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  • 1990-1994  (10,279)
  • Life and Medical Sciences  (10,278)
  • Nuclear reactions
  • 101
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 27 (1994), S. 286-286 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 102
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 27 (1994), S. 150-160 
    ISSN: 0886-1544
    Keywords: axoneme ; bend propagation ; computer simulation ; flagella ; microtubule sliding ; motility ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The distinct damped, or attenuated, bending pattern observed when demembranated sperm flagella of the tunicate, Ciona, are reactivated in the presence of 2 mM Li+ has been analysed in detail. In these patterns, bends are initiated at the base of the flagellum, but die out after they start to propagate along the flagellum, so that little or no bending is seen in the distal half of the flagellum. A quantitative descriptive analysis shows that the distinctive feature of this attenuation of bending wave amplitude is an asymmetric interbend decay, or slippage, occuring, on average, only at the transitions between a reverse bend and the preceding principal bend. This attenuation is combined with a significant amount of synchronous sliding in the distal half of the flagellum and a decrease in propagation velocity of transitions between bends in the mid-region of the flagellum.Computer simulations demonstrate that the synchronous sliding in the distal half of these flagella can be an entirely passive consequence of the mechanical interaction between active sliding and bending in the basal third of the flagellum and viscous resistances to movement of the distal region of the flagellum through the fluid environment. The current computer models do not contain a mechanism for asymmetric interbend decay that can reproduce these attenuated bending patterns. © 1994 Wiley-Liss, Inc.
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  • 103
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 28 (1994), S. 135-142 
    ISSN: 0886-1544
    Keywords: bidirectional swimming ; flagellar movement ; helical bends ; 9+0 axoneme ; planar bends ; viscosity ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Spermatozoa of the small myzostomid worm Myzostomum cirriferum usually swim with the flagellum foremost but occasionally stop and then swim with the head foremost. The spermatozoa have axoneme of the 9+0 type; thus each lacks the central pair microtubules. The flagellum emerges in the anterior end of the cell body and attaches to it with junctions. To understand the mechanism regulating the swimming direction of the spermatozoa, we recorded the sperm and their flagellar movements using a video camera with a high-speed shutter. The effects of calcium and viscosity on these movements were also examined.The cell body with the flagellum attached to it formed a curved plate during beating, while the free portion of the flagellum beats with small helical bends. Motive force to propel a spermatozoon was mainly due to the bends in the cell body. The spermatozoa reversed the direction of their swimming as a result of a change in the direction of bend propagation. The direction of bend propagation was regulated by calcium; the bends in the cell body propagated from the end of the head toward the free portion of the flagellum at low concentrations of Ca2+, whereas the direction of bend propagation was reversed at high concentrations of this ion. High viscosity of the medium stimulated a change in the direction of bend propagation. © 1994 Wiley-Liss, Inc.
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  • 104
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 28 (1994), S. 143-154 
    ISSN: 0886-1544
    Keywords: microtubule-associated proteins ; microtubule nucleation ; tubulin ; cytoskeleton ; axon ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The neuronal microtubule-associated protein tau has been implicated in the development of axonal morphology including the organization of microtubules into a uniformly oriented array of microtubules commonly referred to as “bundle.” Determination of the functional organization of tau has revealed that regions of tau protein which flank the microtubule-binding domain affect the bundling of microtubules in vitro with a microtubule-binding fragment of tau being most effective [Brandt and Lee, 1993: J. Biol. Chem. 268:3414-3419]. In order to study the relation of microtubule bundles that form in vitro to those observed in the axon, we determined the orientation of individual microtubules in bundles and the effects of bundling on microtubule assembly and stability in cell-free assembly reactions. Here we report that bundles induced by a microtubule-binding fragment of tau contain randomly oriented microtubules as determined by using the difference in growth rates at microtubule plus and minus ends. We demonstrate that in vitro bundling increases microtubule growth (about 30%), stabilizes microtubules against dilution- and cold-induced disassembly, and allows microtubule nucleation despite the absence of a tau region which has previously been shown to be required for tau-dependent microtubule nucleation. We conclude that conditions that stabilize microtubules can lead to bundle formation and allow microtubule assembly by a mechanism different from that employed by microtubule-associated proteins. The data also support the view that additional mechanisms besides the action of tau and tubulin exist in order to organize microtubules in the axon. © 1994 Wiley-Liss, Inc.
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  • 105
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    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 29 (1994) 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 106
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 28 (1994), S. 346-358 
    ISSN: 0886-1544
    Keywords: Listeria monocytogenes ; actin ; alpha-actinin ; actin polymerization ; assembly ; disassembly ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Listeria monocytogenes can penetrate and multiply within a variety of cell types, including the PtK2 kidney epithelial line. Once released within the cytoplasm, L. monocytogenes acquires the capacity for rapid movement through the host cell [Dabiri et al., 1990: Proc. Natl. Acad. Sci. 87:6068-6072]. In the process, actin monomers are inserted in proximity to one end of the bacterium, forming a column or tail of actin filaments [Sanger et al., 1992: Infect. Immun. 60:3609-3619]. The rate of new actin filament growth correlates closely with the speed of bacterial migration. In this study we have used fluorescently labeled actin and alpha-actinin to monitor the movement and turnover rate of actin and alpha-actinin molecules in the tails. The half-lives of the actin and alpha-actinin present in the tails are approximately the same: actin, 58.7 sec; alpha-actinin, 55.3 sec. The half-life of alpha-actinin surrounding a dividing bacterium was 30 sec, whereas its half-life in the tails that formed behind the two daughter cells was about 20-30% longer. We discovered that the speeds of the bacteria are not constant, but show aperiodic episodes of decreased and increased speeds. There is a fluctuation also in the intensities of the fluorescent probes at the bacterium/tail interface, implying that there is a fluctuation in the number of actin filaments forming there. There was no strong correlation, however, between these fluctuating intensities and changes in speed of the bacteria. These measurements suggest that while actin polymerization at the bacterial surface is coupled to the movement of the bacterium, the periodic changes in intracellular motility are not a simple function of the number of actin filaments nucleating at the bacterial surfaces. © 1994 Wiley-Liss, Inc.
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  • 107
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 29 (1994), S. 20-28 
    ISSN: 0886-1544
    Keywords: proliferation ; large T antigen ; peripheral nervous system ; cytoskeleton ; microtubules ; myelination ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Schwann cells (SC), the myelinating cells of the peripheral nervous system, show a remarkable capacity to switch from a differentiated state to a proliferative state both during development and peripheral nerve regeneration. In order to better understand the regulatory mechanisms involved with this change we are studying a Schwann cell line transfected with the SV-40 large T gene (TSC). Serum-free medium combined with elevating intra-cellular cAMP levels produced a slower proliferating TSC whose morphology changed from pleiomorphic to process bearing, reminiscent of primary SC in culture. This change was abrogated by colcemid but was unaltered by cytochalasin D, indicating a major role for microtubules. Ultrastructural studies demonstrated numerous microtubules in the cellular extensions which correlated with strong immunocytochemical staining for tubulin in the processes. Analysis of cytoskeletal fractions from the treated cells revealed a greater proportion of tubulin in the polymerized state compared with untreated cells which closely resembled the distribution in primary SC. The cytoskeletal changes observed in the TSC as a result of elevating the intra-cellular cAMP levels may reflect the earliest cellular changes in the induction of myelination. © 1994 Wiley-Liss, Inc.
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  • 108
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    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 29 (1994), S. 110-116 
    ISSN: 0886-1544
    Keywords: high-molecular weight MAPs ; microfilaments ; microtubules ; low-shear viscometry ; taxol ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: High molecular weight microtubule-associated proteins MAP1A and MAP2 form thin projections from microtubule surfaces and have been implicated in crosslinking microtubules and other cytoskeletal components. We have purified native MAP1A from bovine brain and have studied its interaction with G- and F-actin. Using a solid-phase immunoassay we show that MAP1A binds in a dose-dependent manner to both G-actin and F-actin. Addition of MAP1A to F-actin causes gelation of F-actin and SDS-PAGE analysis shows that MAP1A co-sediments with the gelled network, under conditions where F-actin alone does not pellet. The low apparent viscosity of F-actin is markedly increased in the presence of MAP1A, suggesting that MAP1A can crosslink F-actin. Co-incubation experiments indicate that MAP1A and MAP2 may bind to common or overlapping sites on the actin molecule. The widespread distribution of MAP1A and its interaction with microtubules, actin, and intermediate filaments suggests that it may constitute an important determinant of neuronal and non-neuronal cellular morphology. © 1994 Wiley-Liss, Inc.
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  • 109
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 29 (1994), S. 97-109 
    ISSN: 0886-1544
    Keywords: calcium ; flagellar movement ; mechanotransduction ; mechanoshock response ; Spermatozopsis similis ; video analysis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The biflagellate green alga Spermatozopsis similis exhibits a remarkable avoidance reaction in addition to the photophobic or stop response characteristic of such algae. S. similis normally swims forward with its anteriorly attached flagella directed posteriorly and propagating sine-like waves from base to tip. Upon contact with surfaces or other cells, S. similis responds with rapid backward swimming, covering distances of up to 50 μm in 140 to 220 msec. This reaction, which we term the mechanoshock response, also can be triggered by vigorous mechanical stimulation, but not by physiological light intensities. It consists of 3 phases: (1) a rapid acceleration phase with average duration of 31 msec; (2) a phase of about 66 msec with constant high speed (maximal velocities of 〉 600 μm·sec-1) or slow deceleration; and (3) a deceleration phase of ∼ 83 msec, followed by a stop or short period of circling. The cells then resume forward swimming in a random direction. Prior to the mechanoshock response the flagella rapidly are brought together into a close parallel configuration extending anteriorly of the cell body. They then appear to propel the cell by undulatory beating, while the cell describes a pronounced helical path. Small decreases in the extracellular Ca2+ concentration, as well as low concentrations of Ba2+, strongly suppress the probability of this phobic reaction. We conclude that this mechanoshock response involves large Ca2+ influxes, probably mediated by mechanosensitive and/or stretch-activated ion-channel(s). © 1994 Wiley-Liss, Inc.
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  • 110
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 29 (1994), S. 117-130 
    ISSN: 0886-1544
    Keywords: microtubules ; tau ; microfilament-associated proteins ; actin filaments ; growth cones ; antisense oligonucleotides ; cell culture ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We report here a novel intracellular localization and function of Tau proteins in cultured cerebellar neurons. Immunofluorescence staining of detergent-extracted cytoskeletons with antibodies specific for Tau proteins revealed intense labeling of growth cone microtubules. Besides, suppression of Tau by antisense oligonucleotide treatment results in the complete disappearance of antigen 13H9, a specific growth cone component with properties of microfilament- and microtubule-associated protein [Goslin et al., 1989: J. Cell Biol. 109:1621-1631], from its normal intracellular location. This phenomenon is unique to neurite-bearing cells, is not associated with the disappearance of microtubules from growth cones, and is not reversed by taxol, a microtubule-stabilizing agent. In addition, Tau-suppressed neurons display a significant reduction in growth cone area and fillopodial number; on the contrary, fillopodial length increases significantly. The alterations in growth cone morphology are accompanied by considerable changes in the phalloidin staining of assembled actin. Taken together, the present results suggest that in developing neurons Tau proteins participate in mediating interactions between elements of the growth cone cytoskeleton important for maintaining the normal structural organization of this neuritic domain. © 1994 Wiley-Liss, Inc.
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  • 111
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 28 (1994), S. 34-44 
    ISSN: 0886-1544
    Keywords: exocrine gland ; protein secretion ; microtubule-disrupting drugs ; immunofluorescence microscopy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The role of microtubules in the exocrine secretory process is not yet well established, and their disruption by anti-microtubule drugs leads to variable effects on intracellular transit and protein secretion. We investigated the involvement of microtubules in the regulated secretory process of rat parotid glands using microscopic techniques and pulse-chase experiments. We showed that 10 μM colchicine or nocodazole destroys the microtubule network in parotid acinar cells but only weakly reduces the release of newly synthesized proteins. The half-effect was obtained with 0.22 μM colchicine. Moreover, this small reduction was found to be independent of the nature of the drug (colchicine, colcemid, or nocodazole) and of the nature of the stimulation (β-adrenergic or cholinergic pathways). Using nocodazole, we have been able to determine that the steps affected by the drug are very early events in the secretory pathway. Finally, we showed by kinetic analysis that microtubule disruption slows protein release only moderately but does not reduce the total amount of secreted protein. We conclude from this study that microtubule integrity is not essential for protein secretion in rat parotid gland. © 1994 Wiley-Liss, Inc.
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  • 112
    ISSN: 0886-1544
    Keywords: actin filaments ; cytokinesis ; phagocytosis ; contractile vacuole ; immunofluorescence ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Dictyostelium discoideum amoebae possess eight different actin crosslinking proteins. Immunofluorescence microscopy has been employed in this study to investigate the intracellular localization of two of these proteins, α-actinin and the 30 kD actin-bundling protein, to investigate whether they are redundant, or alternatively, make distinct contributions to cell structure and movement. The 30 kD protein is concentrated in the cleavage furrow of dividing cells, while enhanced staining for α-actinin is not apparent in this region. By contrast, α-actinin is concentrated around the contractile vacuole, while the 30 kD protein is not preferentially localized in the area of this organelle. Association of α-actinin with the contractile vacuole was confirmed by colocalization with calmodulin, a marker of this organelle. There are temporal differences in the localization of the 30 kD protein and α-actinin during phagocytosis. The 30 kD protein is localized in the phagocytic cup, but disassociates from phagosomes soon after internalization [Furukawa et al., 1992: Protoplasma 169: 18-27]. α-actinin enters the phagocytic cup after the 30 kD protein, and remains associated with the phagosome after the 30 kD protein has disassociated. These results support the hypothesis that α-actinin and the 30 kD protein play distinct roles in cell structure and movement in Dictyostelium. © 1994 Wiley-Liss, Inc.
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  • 113
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 29 (1994), S. 141-154 
    ISSN: 0886-1544
    Keywords: dynein arms ; nexin links ; radial spokes ; relaxation oscillator ; doublet microtubules ; biological oscillators ; computer model ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Ciliary and flagellar motion is driven by the dynein-tubulin interaction between adjacent doublets of the axoneme, and the resulting sliding displacements are converted into axonemal bends that are propagated. When the axoneme is bent in the normal beating plane, force develops across the axoneme in the plane of the bend. This transverse force (t-force) has maximal effect on the interdoublet spacing of outer doublets 2-4 on one side of the axoneme and doublets 7-9 on the opposite side. Episodes of sliding originates as the t-force brings these doublets into closer proximity (allowing dynein bridges to form) and are terminated when these doublets are separated from each other by the t-force. A second factor, the adhesive force of the dynein-tubulin attachments (bridges), also acts to pull neighboring doublets closer together. This force resists termination of a sliding episode once initiated, and acts locally to give the population of dynein bridges a type of excitability. In other words, as bridges form, the probability of nearby bridges attaching is increased by a positive feedback exerted through the interdoublet spacing. A conceptual working hypothesis explaining the behavior of cilia and flagella is proposed based on the above concepts. Additionally, the feasibility of this proposed mechanism is demonstrated using a computer simulation. The simulation uses a Monte Carlo-type algorithm for dynein attachment and adhesive force, together with a geometric evaluation of the t-force on the key microtubule pairs. This model successfully develops spontaneous oscillations from any starting configuration (including a straight position). It is compatible with the physical dimensions, mechanical properties and bridge forces measured in real cilia and flagella. In operation, it exhibits many of the observed actions of cilia and flagella, most notably wave propagation and the ability to produce both cilia-like and flagella-like waveforms. © 1994 Wiley-Liss, Inc.
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  • 114
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 29 (1994), S. 167-176 
    ISSN: 0886-1544
    Keywords: NuMA ; spindle ; nuclear matrix ; core filaments ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Using a monoclonal antibody 2D3 generated against a kinetochore-enriched human chromosome preparation, we identified a high molecular mass protein with nuclear staining in interphase and polar staining of the pericentriolar region in the mitotic spindle. Initially termed centrophilin, this protein associates with the minus-ends of spindle microtubules (MT) and appears to be important in spindle organization [Tousson et al., 1991: J. Cell Biol. 112:427-440]. Comparison of a partial cDNA sequence obtained for centrophilin with the full length cDNA sequence of nuclear mitotic apparatus protein (NuMA) [Compton et al., 1992: J. Cell Biol. 116:1395-1408; Yang et al., 1992: J. Cell Biol. 116:1303-1317] has indicated that NuMA and centrophilin are the same protein. Using a polyclonal NuMA antibody, we have provided further evidence that NuMA exists as iso-forms as shown by peptide mapping and immunoblots. Sequential fractionation experiments along with immunofluorescence, immunoblotting, and EM immunogold labeling have demonstrated that NuMA isoforms are novel components of nuclear core filaments. Thus, NuMA, a long coiled-coil protein, appears to have dual functions in interphase and mitosis during the cell cycle. In interphase, NuMA likely plays a structural role in the nucleoskeleton that may be important in nuclear organization and functions, whereas in mitosis, NuMA appears to be associated with spindle MT organization and chromosome positioning. © 1994 Wiley-Liss, Inc.
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  • 115
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    Cell Motility and the Cytoskeleton 29 (1994), S. 354-365 
    ISSN: 0886-1544
    Keywords: exocytosis ; rat tumor mast cells ; cytoskeleton ; A23187 ; stress fibres ; tubulin ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Rat basophilic leukemia (RBL-2H3) cells undergo morphological and cytoskeletal changes during antigen-induced secretion of allergic mediators. The exact role these changes play in the process of secretion is unclear. Using confocal microscopy we now show that PMA + A23187 causes extensive F-actin rearrangements during secretion of [3H] 5-HT. We also describe for the first time the association of myosin with F-actin during this secretory process. In unstimulated cells, myosin and F-actin are concentrated at the plasma membrane with no evidence of stress fibres. Upon addition of PMA or A23187, both F-actin and myosin are rearranged into membrane ruffles and discrete aggregations (foci), followed by the formation of parallel stress fibres located on the ventral membrane. This is in contrast to reports in other cell types in which PMA has been described as causing the disruption of F-actin stress fibres. The time course of secretion coincides with the formation of the foci and ruffles whilst the stress fibres form after the majority of secretion has occurred. These changes are accompanied by a 40% decrease in cell height and a two-fold increase in cell spreading and they occur in the absence of extracellular calcium but are inhibited by the protein kinase C inhibitor, Bisindolylmaleimide, which also inhibits secretion. The formation of myosin-decorated stress fibres, foci, and ruffles is not sufficient to cause secretion, as PMA alone induces these changes without any secretion. The relevance of actin and myosin rearrangements for the regulation of secretion is discussed. © 1994 Wiley-Liss, Inc.
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  • 116
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 29 (1994) 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 117
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    Cell Motility and the Cytoskeleton 29 (1994), S. 195-203 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 118
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    Cell Motility and the Cytoskeleton 29 (1994), S. 186-194 
    ISSN: 0886-1544
    Keywords: sperm motility ; intermittent swimming ; Arenicola marina ; annelida ; polychaeta ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Motile spermatozoa of the polychaete Arenicola marina were observed to swim intermittently. On the basis of the behaviour of the flagellum, the quiescent periods can be classified into two main types. The first are those in which, although the generation of the flagellar wave appears to be initiated, its passage down the axoneme appears blocked. This results in the formation of an acute bend (of approximately 2.65 rad) in the proximal region of the flagellum with the remainder of the axoneme remaining straight. These have been termed Type I quiescent periods and are very similar to the “cane-shaped” configuration which has been described in the spermatozoa of some sea urchins. Sperm may also enter a Type II quiescent period, in which both the propagation and the generation of flagellar waves appears blocked. The flagellum of such sperm appears straight or slightly curved and they can remain in this configuration for several minutes. With increased intensity and duration of irradiation, the length of time spent in Type II quiescent period was increased significantly. Both types of quiescent period were (1) reduced in duration and frequency by deletion of calcium from artificial sea water (ASW); (2) either abolished or reduced in duration by the addition of 1 mM cadmium chloride to ASW. In addition, flagellar waveforms very similar to those displayed by spermatozoa in Type I quiescent periods could be induced (if only for a short time) by the addition of the divalent cation ionophore A23187 to ASW. It is suggested that this type of behaviour may be induced following an influx of calcium into the intraflagellar compartment of spermatozoa and that this may be mediated by certain intensities and wavelengths of light. © 1994 Wiley-Liss, Inc.
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  • 119
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    Cell Motility and the Cytoskeleton 29 (1994), S. 383-383 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 120
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    Cell Motility and the Cytoskeleton 29 (1994), S. 215-224 
    ISSN: 0886-1544
    Keywords: cytoplasmic dynein ; Paramecium ; monoclonal antibody ; 12S dynein ; microtubule gliding ; Km and Vmax ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: In an earlier study we reported the isolation of a cytoplasmic dynein from the cytosol of Paramecium multimicronucleatum. In this study we report the isolation and characterization of two cytosolic axonemal dyneins (22S and 12S) as well as a 19S cytoplasmic dynein from the cytosol of whole or deciliated cells using preformed bovine brain microtubules. These three dynein species were characterized according to mass, morphology, vanadate photocleavage patterns, CTPase/ATPase ratios, Km and Vmax values, temperature optima and reactivity with a mAb. For comparison, 22S and 12S axonemal dyneins (ADs) were also isolated and purified from the demembranated axonemes. The 22S and 12S soluble dyneins appear to be related to ciliary ADs in that the 22S soluble dynein is three-headed while the 12S is a one-headed dynein, as determined by negative staining. Ciliary ADs and their corresponding 22S and 12S soluble dyneins isolated from the cytosol also have similar Km and Vmax values as well as vanadate photocleavage patterns and temperature optima. A mAb raised against the soluble 22S dynein reacted with the 22S ciliary dyneins but not the 12S axonemal or the 19S cytoplasmic dynein. All isolated dyneins supported similar microtubule gliding rates but had different ionic requirements for the translocation buffer. These results suggest that: (i) the two soluble 22S and 12S dyneins are precursor molecules of the ciliary dyneins, (ii) the subunits of the outer arm dynein are already assembled in the cytosol as a three-headed bouquet, and (iii) the 22S and 12S soluble dyneins are functional prior to being transported and attached to the axonemes of the cilia. © 1994 Wiley-Liss, Inc.
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  • 121
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    Cell Motility and the Cytoskeleton 29 (1994), S. 231-240 
    ISSN: 0886-1544
    Keywords: cell motility ; scanning acoustic microscopy ; domains of motility ; mechanical properties of the cell ; neoplastic cells ; metastasis ; malignancy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Scanning acoustic microscopy (SAM) observes all mechanical properties of living cells. Subtraction of the SAM images (SubSAM) of live cells was developed as a method for investigating minimal changes in cellular topography and elasticity. The image formation in the SubSAM takes into account the motion of cell mass as well as the changes of tension. High spatial and temporal resolution of the SubSAM revealed the structure of motile processes that develops at increasing time intervals, thus allowing the arising complexity of motion to be registered and investigated. Independent spots of activity emerge on a quiescent background as motility domains; they may change position, divide, merge, or disappear after a long time interval. In addition, zones of quiescence were identified over central parts of cytoplasmic lamellae. Nonmalignant (Ep: tadpole epidermal cells, XTH2: endothelial cells from tadpole hearts, 3T3 cells) and neoplastic cells (K2 cells of rat fibrosarcoma, A870N cells selected from K2) were investigated with the SubSAM. Three types of domains of subcellular cytoplasmic motility were identified in time series of two-dimensional SubSAM images in normal and neoplastic cells. Of them only the wave-like domain is self-evident, being derived from ruffling and protruding activity at the cell margin. Two other domains wait for detailed analysis. The oscillating domain is a visualization of tension within the cell(s), and the nucleating domain indicates intracellular processes possibly preceding locomotion. Differences in motile domains were found between low K2 and high A870N metastatic cells. The dynamics of motility domains of the A870N cells resembled that of the highly motile Ep cells. Cell morphotype and motile activity of the A870N cells are significantly influenced by the pH of the medium. It became evident that identification of the otherwise invisible motile domains in living cells by SubSAM opens a new approach to a characterization of cell motility in vitro and to an understanding of early cellular reactions to various stimuli. © 1994 Wiley-Liss, Inc.
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  • 122
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    Clinical Anatomy 7 (1994), S. 305-314 
    ISSN: 0897-3806
    Keywords: human heart ; membranous ventricular septum (MVS) ; Life and Medical Sciences ; Miscellaneous Medical
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: One of the most common congenital abnormalities of the human heart is a defect in the development of the membranous part of the ventricular septum which, in this study, is designated the MVS. The WS is a thin fibrous membrane, about 1 cm long, which extends upward and to the right from the muscular ventricular septum to the adjacent part of the aortic fibrous annulus that also gives attachment to the right posterior (noncoronary) and anterior (right coronary) aortic valve cusps. It is of considerable clinical importance that there lies between the muscular ventricular septum and the MVS the atrioventricular (AV) bundle of the cardiac conduction system. The MVS has an irregular quadrangular form and has right and left surfaces. This study is based on macroscopic and histological sections of more than 30 normal and abnormal hearts. © 1994 Wiley-Liss, Inc.
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  • 123
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    The @Anatomical Record 238 (1994), S. 57-67 
    ISSN: 0003-276X
    Keywords: Scanning electron microscopy ; Lung fibrosis ; Corrosion casts ; Bleomycin ; Blood vessels ; Endothelial cell ; Collagen ; Bronchi ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: We have used intratracheal instillation of bleomycin in rats to study the microanatomical changes of blood vessels associated with lung fibrosis. Bleomycin is a toxic cytostatic drug employed in classical models of lung fibrosis. Wistar rats were submitted to intratracheal injection of 1.5 units of bleomycin and sacrificed 2.5 months later, a timing when marked fibrosis of the lung is observed. We casted the vascular tree of the rat lungs by perfusion with a methacrylate resin. These caste were studied by scanning electron microscopy. Lung tissue was also studied by light microscopy and thin section electron microscopy. The major vascular modifications observed in the bleomycin-treated rats were: (1) neoformation of an elaborate network of vessels located in the peribronchial domains of the lung, and (2) distortion of the architecture of alveolar capillaries. By light microscopy, it was clear that the newly formed vascular network was located in regions of fibrosis (which in the resin casts were digested away). These neoformed vessels appeared to originate from bronchial arteries. Thin section electron microscopy revealed that endothelial cells of the neoformed vessels were plump, presented large nuclei, and showed numerous pinocytotic vesicles that were also observed in subendothelial pericytes. The alveoli of the bleomycin-treated rats were heterogeneous in size and shape in contrast with the homogeneity of alveoli of control animals. The alveolar capillaries of fibrotic lungs appeared to occupy a larger volume of the alveolar wall than alveolar capillaries of control rats. Our findings indicate that lung fibrosis encompasses marked changes of the vascular system, namely, the neoformation of vessels and the rearrangement of alveolar capillaries. These structural changes suggest that fibrotic transformation of the lung is associated with the local generation of angiogenic stimuli. © 1994 Wiley-Liss, Inc.
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  • 124
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    The @Anatomical Record 238 (1994), S. 68-76 
    ISSN: 0003-276X
    Keywords: Angiogenesis ; Veins ; Endothelial cells ; Prostaglandins ; Microcirculation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The formation of new capillaries from the rat femoral vein was specifically explored to assess whether venous vessels of this caliber may participate in the process of angiogenesis. Prostaglandins of the E series (PGE1 and PGE2) were administered into the soft connective tissue surrounding the rat femoral vessels as angiogenic inducers. In these conditions, between 2 and 7 days, a great number of new capillaries were observed in the media of the femoral vein, arising from the endothelial cells (EC) in the intima. The events of the capillary growth from the femoral vein included EC activation, local degradation of the basal membrane followed by migration and proliferation of EC, solid sprout formation with posterior canalization, development of a new basal membrane, and appearance of pericytes around the new capillary. Although numerous vascular buds were also observed arising from the small venules and capillaries in the periadventitial tissues, they were separated at first from those in the media of the femoral vein by the venous adventitia. Later, connections were observed between both newly formed microcirculations. The present study shows the capacity of PGE1 and PGE2 in the extravascular position of inducing capillary sprouting from veins. Furthermore, the observations provide greater evidence that vessels with characteristics similar to those of the rat femoral vein may contribute to angiogenesis, on occasion with an intense neovascularization. This fact may be of interest for the establishment of a functional circulation after angiogenesis by anastomoses of the new capillaries with those arising from pre-existing vessels of greater caliber than the venules. © 1994 Wiley-Liss, Inc.
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  • 125
    ISSN: 0003-276X
    Keywords: Bimodal breathing ; Cardiovascular ; Pseudobranch ; Choroid plexus ; Lentiform body ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The macrocirculation in the head of three air-breathing species of Channa was examined with the aid of vascular corrosion replicas and a scanning electron microscopic study was conducted on the pseudobranch, choroid gland and lentiform body. Two facultative air-breathing murrles, C. punctata and C. gachua, and one obligate air-breather, C. marulius were examined. In all three, the air-breathing organs (ABO) and systemic circulations were in-parallel, and both were in-series with the branchial circulation. Efferent branchial arteries from the first and second gill arches formed the arterial supply to the ABO, whereas the third and fourth arch efferents perfused systemic tissues. Postbranchial blood from the second gill arch also entered the systemic circulation directly via a shunt from the efferent branchial artery to the lateral aorta and via hypobranchial arteries. Vascular specialization to prevent mixing of oxygenated ABO venous and deoxygenated systemic venous blood was evident in arterial, but not venous circuits. Pseudobranchs of C. gachua and C. punctata are tri-lobed, in C. marulius they have numerous lobules. Pseudobranch lamellae are wider and shorter along the axis of blood flow than gill lamellae and folded perpendicular to this axis. Pseudobranch lamellae appear to be modified to minimize their epithelial surface while retaining an extensive vascular endothelial-pillar cell surface area, counter-current amplification is also possible. The choroid gland is an extensive planar counter-current capillary rete. The lentiform body of the eye is a globular capillary rete but there is no evidence of a counter-current circulation. The choroid and lentiform rete may have distinct physiological functions. © 1994 Wiley-Liss, Inc.
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  • 126
    ISSN: 0003-276X
    Keywords: Cardiovascular ; Endothelium ; Shunt ; Vascular corrosion replica ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Snakehead fish of the genus Channa have well-developed air-breathing organs (ABO) yet retain their gill arches for respiratory and non-respiratory functions. Alterations in the macrocirculation accompany inclusion of the ABO and appear to enhance gas exchange efficiency (Munshi et al., 1994. Anat. Rec. 238:77-91). In the present study, the microcirculatory anatomy of gill and ABO from two facultative air-breathing Channa, C. punctata and C. gachua, and one obligate air-breather, C. marulius, were examined in detail using scanning electron microscopy (SEM) of vascular corrosion replicas and fixed whole-sectioned tissue. The results show that the circulation in the filaments from the first, second, and third gill arches is similar to that found in water-breathing teleosts. Fourth gill arch microcirculation of C. punctata is not different from the other three, whereas in C. marulius, it has been greatly modified into a network of low-resistance vascular shunts, although remnants of an intralamellar filamental microcirculation remain. The vascular shunts are formed from extensions of afferent and efferent lamellar arterioles and the complete, or nearly complete, loss of a lamellar sinus. The vasculature of the ABO has been highly modified in all species into a coiled-spiral capillary network with a constricted aperture guarding a dilated capillary dome at the epithelial surface. Microvilli are found congregated on the aperture endothelium of C. punctata but they are virtually absent from C. marulius endothelium. Less than 15% of the ABO capillary surface appears to face the epithelium and thereby contributes directly to gas exchange. These findings suggest that the microvascular modifications observed in Channa entail more than a simple increase in the contact surface between ABO vessels and air and they may serve other unknown physiological functions. © 1994 Wiley-Liss, Inc.
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  • 127
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    The @Anatomical Record 238 (1994), S. 108-113 
    ISSN: 0003-276X
    Keywords: Computer ; Reconstruction ; Primary palate ; Human ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Our knowledge of the precise spatial relationships of human primary palate morphogenesis remains poorly defined. This is due to intrinsic difficulties that exist in the study of the subject matter and a lack of adequate methodologies. We present a novel new method to allow precise three-dimensional (3-D) visualization of developing embryonic structures in previously sectioned embryos. In our study we focus on human primary palate development. Five normal human embryos from the Carnegie collection were used. 3-D reconstructions appear similar to scanning electron micrographs (SEM); however, unlike in SEM studies, the original specimen has been previously sectioned histologically. 3-D reconstruction from serial sections involved (1) histological preparation of specimen, 2) projection onto digitizing board, 3) digitization, 4) automated reassembly, and 5) relay to interactive optical disc recorder. Detailed observations of each reconstruction were then made. Data generated in this manner may also be used in the near future for quantitative morphometrics. Thus, 3-D reconstruction techniques presented in this paper generated precise spatial information on the development of the human primary palate. © 1994 Wiley-Liss, Inc.
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  • 128
    ISSN: 0003-276X
    Keywords: Striatum ; Caudate nucleus ; Striatopallidal projections ; Striatoentopeduncular projections ; Striatonigral projections ; Cat ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: This study explores the organization of the striatal projections from the rostral caudate nucleus to the output nuclei of the basal ganglia in the cat. Tracer deposits were stereotaxically injected in different dorsoventral, mediolateral, and rostrocaudal sectors of the head of the caudate nucleus using horseradish peroxidase (HRP) conjugated with wheat germ agglutinin (HRP-WGA) either alone or mixed with free HRP. After the injections, a detailed analysis of the terminal labeling was carried out within the globus pallidus (GP), the entopeduncular nucleus (Ep), and the substantia nigra (SN) pars reticulata (SNR). Our findings illustrate how different dorsoventral, mediolateral, and rostrocaudal parts of the rostral caudate nucleus project primarily to similarly positioned but spatially segregated parts of GP. The striatoentopeduncular pathway was also organized topographically, but there was overlapping by projections from different parts of the rostral caudate nucleus. Areas of topographical segregation and zones of overlap were detected in the organization of the striatal projections from the rostral caudate nucleus to SNR. These results raise the possibility of distinct striatal actions upon different sectors of the output nuclei of the basal ganglia and, indirectly, upon their targets in the thalamus and brainstem. © 1994 Wiley-Liss, Inc.
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  • 129
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    The @Anatomical Record 238 (1994), S. 125-130 
    ISSN: 0003-276X
    Keywords: Piriformis ; Superior gluteal nerve ; Innervation ; Human gross anatomy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: In order to examine the relationships between the positional arrangement and supplying nerves of the glutei medius and minimus and the piriformis, we investigated 49 pelvic halves of 28 cadavers. The superior gluteal nerve ran on the ventral surface of the piriformis in 44 cases (89.8%) (Type A), and some branches of the nerve perforated the piriformis in five cases (10.2%) (Type B). Based on the detailed findings of the innervation of the three muscles, the piriformis is chiefly composed of the caudal element of the gluteus medius (Type A) and in some cases the caudal element of the gluteus minimus as well (Type B). © 1994 Wiley-Liss, Inc.
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  • 130
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    The @Anatomical Record 238 (1994), S. 147-147 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 131
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    The @Anatomical Record 238 (1994) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 132
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    The @Anatomical Record 238 (1994), S. 131-146 
    ISSN: 0003-276X
    Keywords: Thumb ; Muscle ; Proprioception ; Opposition ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The observation of thirty dissections of intrinsic muscles of the thumb provides some information differing from earlier anatomical studies. The abductor pollicis brevis and the opponens pollicis have been divided into muscles having six or two fascicles (or bellies), respectively. The adductor pollicis muscle has been separated into nine fascicles. Many variations were observed: absence of fascicles, presence of atrophied or supplementary fascicles, or fascicles with varying insertions sites. Neither head of the flexor pollicis brevis muscle seemed to have any fascicles. The distal insertion of its superficial head observed in this work is not in accordance with the usual description found in the literature. A new classification of the thenar muscles is presented based on the present observations. Many variations were observed: some fascicles were absent, others were supplementary or atrophied, and some had variable insertions. The importance and the individual variations of the fascicles are discussed. © 1994 Wiley-Liss, Inc.
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  • 133
    ISSN: 0003-276X
    Keywords: Human dermis ; Collagen fibers ; Elastic fibers ; Morphometric analysis ; Aging ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Normal human dermis has been analyzed using sterological methods to estimate the quantitative modifications of collagen and elastic fibers in relation to age, sex, and body region. Forty-five skin biopsies from the trunk or the limbs of 26 males and 19 females of different age were fixed in glutaraldehyde and osmium tetroxide and embedded in epoxy resin. The relative volumes of collagen and elastic fibers were calculated by the point counting method on 1 μm semithin sections. Photographic sampling was performed on four consecutive dermis layers: the papillary layer and three consecutive layers of reticular dermis. The data were subjected to analysis of variance which showed that all the factors studied exert a significant influence on the relative amounts of collagen and elastic fibers. The fractional volume of collagen fibers is constant throughout all dermis layers analyzed and is always higher in females than in males, except for the second and third decades of life. Collagen fiber density increases with age in both sexes up to 30-40 years, when it starts decreasing. Both the relative volumes and the diameters of elastic fibers increase from papillary to deep reticular dermis. In reticular dermis of both sexes there is an increment of elastic fiber density in the first decade of life, followed by a drop particularly marked in males. After 20 years, the relative volume of elastic fibers displays a decreasing trend in females, whereas it increases in males, attaining the highest values beyond the 40s. © 1994 Wiley-Liss, Inc.
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  • 134
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    The @Anatomical Record 238 (1994), S. 163-176 
    ISSN: 0003-276X
    Keywords: Endometrium ; Rat ; Estrus cycle ; Electron microscopy ; Sex hormones ; Morphometry ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Studies on the endometrial cycle depend upon the precise dating of the cycle stage. In the present paper the generally applied method of vaginal smear was carefully verified through the measurement of the hormones relevant to the endometrial cycle. From rats predated through vaginal smear cytology, the hormone levels of estradiol-17-beta (E2) and progesterone (P), luteinizing hormone (LH), and follicle stimulating hormone (FSH) were measured. The values obtained were then compared to the standardized values of our reference curve. Animals with values that did not fit within the standard deviation of our reference curve were excluded from this investigation. Thus, for the first time exactly dated rat endometrial morphology was studied with electron microscopy. The morphology of the surface epithelium of rat endometrium from all four stages of the cycle is described in detail. In addition, a semiquantitative morphometric analysis of the following parameters was performed: cell volume, nuclear volume, the volume density of secretory granules, digestive vacuoles, mitochondria, Golgi apparatus, rough endoplasmic reticulum, and lipid vacuoles as well as the size of lipid vacuoles. With the cellular content of lipid vacuoles and their diameter, it is possible to differentiate between proestrus/estrus and diestrus I/diestrus II, the latter possessing definitely more and larger lipid vacuoles. During estrus the greatest cytoplasmic volume develops. In addition to this, secretory granules are only present during estrus. Finally, diestrus I can be well differentiated from diestrus II, because diestrus I exhibits more digestive vacuoles and during diestrus II a high percentage of free ribosomes is present. On the basis of distinct morphological features, described in this paper, it is now clearly possible to distinguish between the four different cycle stages. © 1994 Wiley-Liss, Inc.
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  • 135
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    The @Anatomical Record 238 (1994), S. 177-190 
    ISSN: 0003-276X
    Keywords: Pig placenta ; Vascularisation ; Scanning electron microscopy ; Implantation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The vascular interrelationship of the well-established porcine placenta has previously been described from vascular casts and histology, but not its developmental stages. This study was peformed using the same methods on 17 sows of well-known stages of gestation ranging from 9 1/2 to 43 days post coitum (p.c.). At the precontact stage, days 9 1/2 to 12 1/2 p.c., the subepithelial capillaries formed a wide open meshwork of variable diameter, 3-14 μm, without any difference between meso- and antimesometrial side. At the early contact and adhesion stages (days 13 to 18 p.c.), the first increase in vasculature was seen at the mesometrial side close to the embryonic disc of the very long blastocyst at day 15 p.c., 2 days after the first contact between trophoblast and maternal epithelium was seen. At day 18 p.c., the areas with dense capillaries increased markedly at the mesometrial side with the same parallel organization as seen at day 15 p.c., whereas the antimesometrial side still had a relative loose appearance comparable to the previous stages. At the early placental stages (days 20 1/2 to 23 p.c.), the capillary bed formed smooth folds, which in some areas at day 20 1/2 days developed into smaller folds or prerugae. Here the capillaries changed to convoluted forms with slightly bulbous dilations measuring about 30-35 μm in diameter. This developmental progress became more elaborate at day 23: capillaries of the low ridges of prerugae formed irregular dilations up to 50 μm in some areas. At this stage the parallel arrangement of the capillary meshwork characteristic of the previous stage was not longer discernable. By days 32-43 p.c., an increase in microscopic folding was present, and the maternal arterioles could be traced to the top of the ridges, creating the characteristic vascular architecture needed for an efficient exchange of oxygen, carbon dioxide, and nutrients of the basically developed porcine placenta. © 1994 Wiley-Liss, Inc.
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  • 136
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    The @Anatomical Record 238 (1994) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 137
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    The @Anatomical Record 238 (1994), S. 1-14 
    ISSN: 0003-276X
    Keywords: Junctional epithelium ; Epithelial attachment ; Cementum ; Extracellular matrix ; Electron microscopy ; Electrophoresis ; Pig ; Rat ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The region of epithelial apposition with a tooth surface is the site of an unusual stratified integument, the junctional epithelium, which combines tight attachment to the tooth, cell turnover, tissue permeability, and epithelial versatility into the first line of defense against periodontal destruction by oral pathogens. To better understand the structure and function of the junctional epithelium we have reviewed its developmental and cell biology, and undertaken a multidisciplinary analysis of its composition in the pig, an omnivore whose dietary and dental development and occlusion patterns are similar to the human condition, and which, because of its size, is more readily amenable to experimental manipulation. The porcine junctional epithelium was also compared with this well-described epithelium in the rat. Morphological analyses by light microscopy and scanning and transmission electron microscopy showed the porcine junctional epithelium and epithelial attachment were similar to that in the rat except that apically, extracellular matrix lamellae associated with the internal basal lamina were more complex, and more coronally there was extensive layering of a dental cuticle-like material. Biochemical analysis of the porcine junctional epithelium by dissociative extraction and SDSPAGE revealed the presence of some proteins not present in gingival epithelium. Together, these studies show that the porcine junctional epithelium has predictable morphological and biochemical features which establish the pig as an advantageous model to study the basic and clinical biology of this unique epithelium. © 1994 Wiley-Liss, Inc.
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  • 138
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    The @Anatomical Record 239 (1994) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 139
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    The @Anatomical Record 239 (1994), S. 1-8 
    ISSN: 0003-276X
    Keywords: Rabbit bone marrow cells ; Fibroblastic cell cultures ; Osteogenic colonies ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: This experiment was designed to test whether a single cell suspension of adult marrow-derived cells will form mineralized bone nodules in vitro. Methods: At the time of plating, cellular dispersions of either young adult rabbit bone marrow cells or, as controls, of fetal mouse calvarial cells were size-selected by sieving through various poresize plastic meshes. Results: When marrow-derived cells were passed through a 105 μm pore-size mesh, fibroblastic cell cultures grew in vitro in six of six attempts; however, marrow cell clusters backwashed off 105 μm pore-size meshes produced osteogenic colonies in vitro in six of six trials. Fetal calvarial cells filtered through a 30 μm pore-size mesh yielded osteogenic nodules in culture in six of six tests. Conclusions: For adult bone marrow, cell clumps or clusters larger than 105 μm produced bone colonies under standard cell culture conditions, whereas for fetal calvarial cells, the initiating agent was smaller than 30 μm. © 1994 Wiley-Liss, Inc.
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  • 140
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    The @Anatomical Record 238 (1994), S. 533-533 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 141
    ISSN: 0003-276X
    Keywords: Fracture-label method ; oviductin ; zona pellucida ; oocytes ; cytochemistry ; scanning electron microscopy ; lectins ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Backscattered electron imaging fracture-label (BEI-FL), an adaptation of the fracture-label method for scanning electron microscopy, offers the advantage of providing information about the distribution of antigenic and receptor sites with respect to the three-dimensional organization of tissues and cells over relatively large surfaces. Recently, using post-embedding cytochemistry on thin-sections of Lowicryl-embedded oocytes, a homogenous distribution of glycoproteins in the zona pellucida (ZP) was demonstrated (Kan et al., 1989. Biol. Reprod., 40:585-598, Anat. Rec., 226:37-47; Roux and Kan, 1991. Anat. Rec., 230:347-360). However, it can be argued that the chemical nature of resins and the physical conditions of tissue processing required for post-embedding cytochemistry may introduce changes in the tissue components and result in altered distribution of components. On the other hand, freeze-fracture exposes constituents in a minimally denaturing manner and, since no embedding media are used, binding sites are sterically available to the probe. We have, therefore, applied BEI-FL to examine the distribution of matrix glycoproteins in the ZP of hamster oocytes.Methods: Ovaries and cumulus masses obtained from superovulated female golden hamsters were fixed by immersion in 2.5% glutaraldehyde and processed for fracture-label. Tissues were labeled, respectively, with Wheat germ agglutinin (WGA) followed by ovomucoid-colloidal gold, Ricinus communis agglutinin I (RCA I)-colloidal gold or a monoclonal antibody against Hamster Oviductin-1 followed by protein A-gold, and then examined in the scanning electron microscope.Results: Backscattered electron imaging revealed a homogenous distribution of WGA and RCA I binding sites throughout the cross-fractured matrix of the ZP of cvrian and postovulatory oocytes. Hamster Oviductin-1, an oviductal glycoprotein which is transferred to the ZP of oocytes during oviductal transit, was also found to be uniformly distributed throughout the ZP of postovulatory oocytes.Conclusions: Our results indicate that BEI-FL can be advantageously used to examine extracellular matrices and are consistent with the concept that glycoproteins are uniformly distributed throughout the ZP of the hamster oocyte. © 1994 Wiley-Liss, Inc.
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    The @Anatomical Record 239 (1994), S. 47-54 
    ISSN: 0003-276X
    Keywords: M cell ; Peyer's patches ; follicle associated epithelium ; mucosal immunity ; Streptococcus pneumoniae R36a ; rabbit ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Lymphoid cells have often been observed in the intestinal lumen and it has been hypothesized that M cells could represent one of the most important migration routes for the immunocompetent cells from the lymphoid follicle to the lumen. However, a direct evidence of the passage was lacking. In this study we describe a morphological analysis of the lymphocyte traffic in rabbit Peyer's patches after an in vivo stimulation with an antigen normally not present in the intestine.Methods: The antigenic stimulation of a large number of Peyer's patches was carried out using the isolated ileal loop technique and then the samples from stimulated and control Peyer's patches were analysed by light and transmission electron microscopy.Results: We have been able to describe details of lymphocyte migration through M cells, from the follicle to the intestinal lumen, and a marked increase of intraluminal lymphocytes by counting the immunocompetent cells after periods of antigenic stimulation of varying lengths.Conclusions: Our finding is that the passage of lymphocytes to the lumen is an antigen-dependent event and we also provide direct evidence that M cells are one of the migration routes. Our observations also indicate that lymphoid cells in the intestinal lumen may play an immunologic role in mucosal immunity. © 1994 Wiley-Liss, Inc.
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  • 143
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    The @Anatomical Record 239 (1994), S. 55-64 
    ISSN: 0003-276X
    Keywords: Carboxylesterases ; Nasal metabolism ; Olfactory toxicity ; Xenobiotic metabolism ; Olfactory mucosa ; Respiratory mucosa ; Human ; Dog ; Rat ; Nasal toxicity ; Nose ; Comparative ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background. Carboxylesterases (CE) exhibit high activity in the nasal mucosae and produce acid metabolites toxic to the olfactory epithelium following exposures to inhaled esters. The regional distribution and activity of CE have been studied in rodents, but no comparative studies have examined regional localization or activity in dog or human nasal tisses.Methods. We determined the immunohistochemical distributions of CE in the nasal respiratory and olfactory mucosae of Beagle dogs, and the nasal respiratory mucosa of the human nose and compared these distributions to those in the F344 rat.Results. In the dog respiratory mucosa, the greatest CE immunoreactivity was in the subepithelial glands and surface epithelial cells. In the olfactory mucosa, immunoreactivity was observed in the apical portion of the sustentacular cells, and in duct cells and acinar cells of Bowman's glands. This distribution is similar to that found in rat, except the subepithelial glands of the rat respiratory mucosa showed little to no immunoreactive CE. The human respiratory mucosa showed immunostaining in surface epithelial cells as well as glandular cells. Immunostaining in the human tissue samples was dramatically reduced in the presence of hyperplastic lesions and virtually eliminated in samples with squamous metaplasia.Conclusions. The data indicate that the distribution of CE is very similar in healthy nasal mucosae across the three species studied. However, the loss of CE immunoreactivity correlated with nasal epithelial lesions in the human samples suggests enzymatic activity may be compromised by insults to nasal tissues. Further studies of CE activity in animals following nasal insult could improve the ability to predict human responses to inhaled esters. © 1994 Wiley-Liss, Inc.
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  • 144
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    The @Anatomical Record 240 (1994), S. 59-76 
    ISSN: 0003-276X
    Keywords: Implantation ; Centric ; Intrusive ; Yolk sac placenta ; Marsupial ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: In marsupials implantation occurs about two-thirds the way through the short gestation before which time the embryo is surrounded by the permeable shell membrane which prevents physical contact between the trophoblast and uterine epithelium. Although the trophoblast has been shown to be invasive to varying degrees in several species of marsupials, the ultrastructure of the embryonic-uterine cell interactions at the time of implantation has not been described in this group.Methods: Thick plastic sections and transmission electron microscopy were employed to investigate the cellular interactions at implantation in the fat-tailed dunnart (Sminthopsis crassicaudata), a dasyurid Australian marsupial.Results: Our results show that epithelial penetration begins when the embryo is at the late presomite/early somite stage. In the trilaminar region of the yolk sac (TYS), trophoblast cells adjacent to the embryo form desmosomes with uterine epithelial cells and also appear to fuse with them to form hybrid cells, the cytoplasm of which resembles that of trophoblast. Later in the TYS, as the placenta develops, trophoblast microvilli and larger cell processes invaginate, and interdigitate with, the highly folded maternal epithelium but do not invade it. At this time in the bilaminar, or avascular, yolk sac (BYS), multinucleate trophoblast giant cells (TGCs) from an annular region adjacent to the sinus terminalis intrude between, and possibly fuse with, the maternal epithelium. The invading TGCs spread laterally above the residual basal lamina before migrating into the stroma.Conclusions: In this species of marsupial at least, the cell interactions at the time of implantation are similar to those seen in some eutherian species despite the fact that the fetal chorion is of yolk sac rather than allantoic origin. © 1994 Wiley-Liss, Inc.
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  • 145
    ISSN: 0003-276X
    Keywords: Hormones ; Porphyrinogenesis ; Castration ; Pinealectomy ; Melatonin ; Pineal gland ; Seasonal changes ; Mesocricetus auratus ; golden hamster ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: The porphyrin concentrations of the Harderian glands of Syrian hamsters show marked sexual differences, with male levels being much lower than those of females. Porphyrinogenesis is inhibited by androgens, so orchidectomy leads to elevated male porphyrin concentrations; however, a number of other procedures (some of which also lower androgen levels) prevent this. We studied the effects of short-day photoperiods and melatonin on Harderian porphyrin concentrations.Methods: Intact, castrated, or pinealectomized hamsters of both sexes were exposed to long-day or short-day photoperiods. Intact or castrated hamsters were given melatonin injections in the morning or the afternoon, or were given beeswax pellets containing melatonin. After a variable period, Harderian glands were dissected and porphyrins were measured.Results: Prolonged short-day exposure (13 weeks) led to increased Harderian porphyrin concentrations and this rise was prevented by pinealectomy. The rise in Harderian porphyrins following short-day exposure was small, compared with that following castration. Short-day photoperiods also prevented the rise in porphyrin levels associated with castration and this effect was prevented by removal of the pineal. Melatonin injections, whether given in the morning or in the afternoon, had no effect on Harderian porphyrin concentration of castrated male hamsters. Continuous release melatonin pellets reduced the postcastrational rise in porphyrin levels in one experiment, while having no effect in another. In female hamster, neither short photoperiods nor melatonin pellets influenced Harderian porphyrin concentrations.Conclusions: These results suggested that a factor from the pineal gland helps maintain the low levels of porphyrin which are characteristic of male Harderian glands, despite the decrease in androgen levels which typically results from exposure to short days. Morning and afternoon injections of melatonin and continuous release melatonin pellets failed to resolve the question of whether this pineal factor is melatonin. Our results demonstrated that low male and high female porphyrin levels are maintained in Syrian hamsters, despite seasonal variations in the hormonal milieu, suggesting that these sexual differences are important for the (still unestablished) function of the Harderian glands in this species. © 1994 Wiley-Liss, Inc.
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  • 146
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    The @Anatomical Record 240 (1994), S. 77-85 
    ISSN: 0003-276X
    Keywords: Reproduction ; Estrous cycle ; Ciliated cell ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: In mammals, the oviductal secretory cells and their secretions play important roles in reproductive and developmental events. Therefore, many electron microscopic studies of mammalian oviductal epithelial cells have been performed.Methods: The secretory cells in various regions of the rat oviduct during the estrous cycle were examined by transmission electron microscopy.Results: In the fimbriae, the secretory cells contained small secretory granules with moderately electron-dense matrices and many large bodies that resembled lipid droplets. In the ampullar cells, small secretory granules with moderately electron-dense matrices were observed in the apical cytoplasm. In the isthmus, the secretory cells contained numerous secretory granules with moderately electron-dense matrices. Electron-dense areas were frequently observed in many of the granules of the isthmic cells. Vesicles, partially filled with a dense substance, frequently were observed in the isthmic cells and occasionally in the ampullar cells. Very long stereocilia projected from the surfaces of the isthmic secretory cells into the lumen. Exocytosis of the secretory granules was observed. In addition, there was evidence to suggest the release of the bodies that resembled lipid droplet occurred. Cysts and ciliated vacuoles that appeared to be intraepithelial were frequently observed in the fimbrial and ampullar epithelia. No dramatic changes in the relative numbers of ciliated and secretory cells in any oviductal segment were observed during the estrous cycle.Conclusions: Our ultrastructural observations of the rat oviduct revealed marked regional variations in the morphological features of secretory cells. These results may provide insight into regional and cellular differences in the function of the rat oviduct. © 1994 Wiley-Liss, Inc.
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  • 147
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    The @Anatomical Record 240 (1994), S. 86-103 
    ISSN: 0003-276X
    Keywords: Immobilin ; Development ; Principal cells ; Clear cells ; Secretion ; Endocytosis ; Rat epididymis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Immobilin is a protein secreted by principal cells of the distal initial segment, intermediate zone and caput epididymidis of adult rats, which serves to immobilize spermatozoa. In the distal cauda, epithelial clear cells are involved in its endocytosis. The objective of this study was to correlate the developmental events in the maturation of the epdidymis with the timing of immobilin secretion and endocytosis in order to evaluate the testicular or epididymal factors which may influence or regulate immobilin expression.Methods: Our approach was to follow and compare the developmental expression of immobilin by light microscope immunocytochemistry in control and efferent duct ligated rats of different postnatal ages.Results: Coincident with the morphological maturation of the principal cells by postnatal day 39, immobilin displayed the characteristic secretory immunostaining pattern found in adults. This adult-like expression occurred despite the absence of spermatozoa in the lumen but was coincident with high levels of circulating and luminal androgens. In contrast, immobilin secretion in rats whose efferent ducts were ligated at day 15 was weak to non-existent in the principal cells of the caput epididymidis at day 28 and remained so into adulthood, indicating that principal cells of this region of the epididymis are dependent either directly or indirectly upon testicular factors present in the lumen for immobilin expression. However, secretion of immobilin in the principal cells of the distal initial segment was unaffected by ligation and unlike the case in control rats high levels of immobilin also continued to be secreted into adulthood by the principal cells of the proximal initial segment. Thus in the distal initial segment immobilin secretion is not regulated by luminal factors originating from the testis, while in the proximal initial segment the normal suppression of immobilin that occurs by postnatal day 39 is. Despite ligation, endocytosis of immobilin by clear cells of the distal cauda epididymidis occurred by day 49, indicating that luminal testicular factors are not essential for stimulating the uptake of immobilin by these cells.Conclusions: The results taken together suggest that there are stimulatory and inhibitory luminal testicular factors involved in the regional development of immobilin secretion in the epididymis. There are also immobilin secreting regions in the epididymis, whose secretory development is independent of luminal testicular factors. © 1994 Wiley-Liss, Inc.
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  • 148
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    The @Anatomical Record 240 (1994), S. 104-114 
    ISSN: 0003-276X
    Keywords: Cerebellar bloodflow ; Endothelial injury ; Subarachnoid hemorrhage ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: The leading cause of death and disability in patients suffering from aneurysmal subarachnoid hemorrhage (SAH) is cerebral vasospasm, a persistent, progressive, and often irreversible constriction of cerebral arteries. A wide array of pathological changes occur in cerebral arteries following SAH, with endothelial injury being the earliest and most consistent one. Since intact endothelium modulates many reflexes that influence vascular tone, damage to them may represent a significant contributor to cerebral vasospasm.Methods: Changes in local cerebellar blood flow (LCBF) and pathological alterations in major cerebral arteries were studied and compared in rats at various time intervals following SAH. SAH induced by the subarachnoid injection of 0.3 ml of whole blood. Sham rats received a subarachnoid injection of 0.3 ml of isotonic saline.Results: Except for an immediate but transient decrease, LCBF remained unchanged over a 3 day period following saline injection. Likewise, there were no pathological alterations in cerebral arteries of saline-injected rats. In contrast, the subarachnoid injection of whole blood produced significant changes in both LCBF and cerebral arteries. Within 30 minutes postblood injection, LCBF became significantly decreased and remained so for 4 hours. However, within 24 hours, LCBF had returned to control levels where it remained for 3 days. Endothelial injury was observed in the basilar and middle cerebral arteries from 30 minutes through 4 hours, the same periods in which LCBF was significantly reduced. Within 24 hours, the time period in which LCBF had rebounded to control ranges, cerebral arteries showed no evidence of endothelial damage and resembled control cells.Conclusion: The results indicate a direct correlation between changes in LCBF and the structural integrity of endothelial cells in the early stages following SAH. The lack of chronically depressed LCBF (after 1 day) may be related to the quick structural repair of endothelium. © 1994 Wiley-Liss, Inc.
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  • 149
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    The @Anatomical Record 240 (1994), S. 115-119 
    ISSN: 0003-276X
    Keywords: ACPI ; Cystatin A ; Thymus ; Thymocyte ; Apoptosis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Acid cysteine proteinase inhibitor (ACPI, also called cystatin A) is a protein that is present in the epithelial cells of the skin and in the dendritic reticulum cells of lymphoid tissues. In this study the presence and cellular localization of ACPI in the thymus was investigated.Methods: The cellular and topographical location of ACPI was immunohistochemically demonstrated in the normal thymus of man.Results: ACPI was found in the cells of the-Hassall's corpuscles and in many medullary cells. Most of these cells were epithelial cells, as shown by the results of immunohistochemical cytokeratin and epithelial membrane antigen stainings. Also, some individual cytokeratin negative but S-100 positive medullary reticular dendritic cells were stained with ACPI.Conclusions: The finding that ACPI is constantly present in the thymus at restricted and specific cellular locations leads to the suggestion that protease inhibitors may play a role in specific thymic functions. © 1994 Wiley-Liss, Inc.
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  • 150
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    The @Anatomical Record 240 (1994), S. 120-124 
    ISSN: 0003-276X
    Keywords: BUN ; Glomerulus ; Maternal uninephrectomy ; Morphometry ; Rat kidney ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: The present study was designed to explore whether maternal renal dysfunction affects fetal kidney development and if the effects are lasting during the postnatal development.Methods: Kidneys of 1-day-old and 6-week-old pups from mothers which were uninephrectomized on day 5 of gestation were studied.Results: One day after birth, both the number of immature glomeruli and average volume of mature glomeruli of the neonates from uninephrectomized mothers were significantly larger than those from sham-operated mothers. Six weeks after birth, no significant differences in parameters of the kidney were observed between the pups from uninephrectomized and those from sham-operated mothers. Furthermore, blood urea nitrogen (BUN) concentration in adult female rats was determined at various days after uninephrectomy. BUN concentration in uninephrectomized rats was significantly higher than that in sham-operated ones.Conclusions: These results suggest that the fetal kidney development is accelerated by the elevated BUN level following maternal uninephrectomy and that the renotropic activity does not last during the postnatal developmental period. © 1994 Wiley-Liss, Inc.
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  • 151
    ISSN: 0003-276X
    Keywords: Epidermal growth factor receptors ; Peripheral nerves ; Sensory corpuscles ; Skin ; Human ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: The epidermal growth factor receptor (EGFr) binds both epidermal growth factor (EGF) and transforming growth factor α (TGFα), which are currently considered among putative growth factors playing a role in the nervous system. EGFr and their ligands have been localized in the mammalian peripheral nervous system. The present study was undertaken to investigate whether nerves and sensory corpuscles supplying human glabrous skin express EGFr.Methods: Formaldehyde fixed, paraffin embedded samples of finger-tip digital skin obtained from adult healthy subjects were processed for indirect PAP immunohistochemistry using a monoclonal antibody against an epitope of the intracellular domain of EGFr. To ascertain the localization of EGFr immunoreactivity, neurofilament proteins (NFP), S100 protein (S100P), and epithelial membrane antigen (EMA) were studied in parallel to label axons, Schwann cells, and perineurial cells, respectively, as well as their corpuscular derivatives.Results: A variable intensity of EGFr immunostaining was regularly observed in the perineurium and Schwann cells, and occasionally in the axons of nerve bundles. EGFr immunoreactivity was also present in the axon and lamellar cells of Meissner corpuscles, and within the axon, inner-core, outer-core, and capsule of Pacinian corpuscles.Conclusions: Present results demonstrate that human cutaneous nerves and sensory corpuscles express EGFr suggesting a role for peptides able to bind EGFr, i.e., EGF and TGFα, in the human peripheral nervous sensory system. © 1994 Wiley-Liss, Inc.
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  • 152
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    The @Anatomical Record 240 (1994) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 153
    ISSN: 0003-276X
    Keywords: Electron microscopy ; Immunocytochemistry ; GABA ; Somatosensory system ; Anterograde tracers ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: The ventropostero lateral nucleus (VPL) is a thalamic somatosensory center receving inputs from limbs and trunk; some of this input is via terminals of the dorsal column medial lemniscal pathway. These fibers convey non-noxious somesthesic information.Methods: In this study the neurochemical content of lemniscal afferents in VPL of rats was investigated at the electron microscopic level by combining anterograde transport of horseradish peroxidase conjugated to wheat germ agglutinin, injected in the dorsal dorsal column nuclei, with postembedding immunogold labeling for glutamate (Glu).Results: Anterograde labeling in VPL was detected only in myelinated axons and in large terminals containing round synaptic vesicles, interpreted as lemniscal afferents. Quantitative evaluation of gold particle density showed enrichment of Glu immunolabeling in the identified lemniscal terminals with respect to other neuronal profiles. Observation of serial sections immunoreacted for Glu demonstrated consistency of labeling, whereas in alternate sections immunoreacted for Glu and for the inhibitory amino acid GABA these two antigens were always present in distinct types of terminals.Conclusions: These findings are in agreement with several lines of evidence, obtained with different experimental approaches, supporting the hypothesis that Glu plays a major role in conveying sensory stimuli to the thalamus from second order neurons in the dorsal column nuclei. © 1994 Wiley-Liss, Inc.
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  • 154
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    The @Anatomical Record 240 (1994), S. 141-147 
    ISSN: 0003-276X
    Keywords: Anteromedial eye ; Retina ; Rhabdom ; Nonpigmented cells ; Capillary ; Liphistiid spider ; Heptathela kimurai (Chelicerata) ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: The presence of efferent fibers in the anteromedial eye of liphistiid spiders kept in natural daily cycles of illuminance has been reported. However, this report is limited to innervation by the efferent fiber and daily rhabdomal changes, and there have been no detailed ultrastructural accounts of the eye.Methods: The fine structure of this eye was examined by electron microscopy.Results and conclusions: The eye consists of a cornea, a lens, a vitreous body, and a retina. The retina contains 13 or 14 receptor cells and glial cells. The rhabdoms are distal to the nuclei of the receptor cells. In the distal region of the receptive segment, the rhabdomeres lie in the center of the cell. In the middle region, anisomorphic rhabdoms formed by microvilli from adjacent cells are at the cell periphery. In the proximal region, the rhabdomeres are situated in the center of the cell. The ocellar nerve of the eye runs toward the protocerebrum and enters the posterior part of the first optic ganglion of the secondary eyes. Pigmented cells and nonpigmented cells are observed. The pigmented cells are located in the most lateral of the eye and cover the whole eye. The nonpigmented cells are located in the receptor cell bodies and extend to the origin of the ocellar nerve. They wind to form capillaries filled with electron-dense material. These structures are discussed in comparison with those of other spiders and other chelicerates. © 1994 Wiley-Liss, Inc.
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  • 155
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    The @Anatomical Record 240 (1994), S. 149-156 
    ISSN: 0003-276X
    Keywords: Cochlea ; Supporting cells ; Morphology ; Ion transport ; Ultrastructure ; Gerbil ; Outer tunnel ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: The mammalian cochlea contains beneath and lateral to outer hair cells, several types of supporting cells. The function of these cells has not been explained beyond providing a structural base.Methods: The supporting cells of gerbil cochlea were examined by electron microscopy with a view to elucidating their biologic activity on the basis of cytologic structure.Results: Ultrastructural examination differentiated the laterally located Hensen cells from their medial neighbor connected to the third Deiters cell. The later cell formed a cover to the outer tunnel between Hensen and Deiters cells, appeared not to reach the basilar membrane, and exhibited a denser cytosol and more mitochondria, compared to Hensen cells. In these respects the cell observed here to cover the outer tunnel, corresponded with the tectal cell described by Henson et al. (1983) in the mustache bat, but not heretofore documented in other animals.Conclusions: This distinctive cell in the gerbil differend in displaying unique villus-like structures which projected from the basomedial surface and are referred to as fimbriae. The fimbriae and interspersed filopodia largely filled outer tunnel space and expanded the cell's basal surface. The amplification of basal plasmalemma by fimbriae and their content of mitochondria testify to a role for the tectal cell in ion resorption and an influence on ion content and volume of outer tunnel fluid. © 1994 Wiley-Liss, Inc.
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  • 156
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    The @Anatomical Record 240 (1994), S. 157-166 
    ISSN: 0003-276X
    Keywords: Atrioventricular valve ; Nerve terminals ; Neuropeptide Y ; Interstitial cells ; Electron microscopy ; Immunogold staining ; Japanese monkey ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Bacground: A rich supply of nerves to the atrioventricular valve has been demonstrated. The role of the valvular nerves is still controversial because the target sites of the nerves have not been confirmed.Methods: The innervation of the atrioventricular valves of the Japanese monkey (Macaca fuscata) was examined by acetylcholinesterase staining and electron microscopy. Immunoreactivity for neuropeptide Y (NPY) was also investigated by a post-embedding immunogold method.Results: The valvular nerve elements were clearly concentrated between the endothelium and interstital cells on the atrial side of cusps. Naked axon terminals were observed to make direct contact (20-nm gaps) with interstitial cells and also to be in close proximity (∼200-nm cleft) to the endothelium. NPY immunoreactivity was clearly detected on the large granular vesicles in some terminals that were in close proximity to interstitial cells and/or the endothelium.Conclusion: The present study suggests that the extensive innervation of the atrioventricular valve, which includes NPY-containing nerves, might affect valvular function via interstitial cells and/or the endothelium. © 1994 Wiley-Liss, Inc.
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  • 157
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    The @Anatomical Record 240 (1994), S. 167-177 
    ISSN: 0003-276X
    Keywords: Tongue ; Anterior lingual glands ; Salivary glands ; Glycoconjugates ; Mucous cells ; Seromucous cells ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Speciamens of human anterior lingual salivary glans obtained by surgery and by dissection of cadavers were studied ultrastructurally and histochemically.Methods: Specimens were obtained by surgery for ultrastructural study. Other specimens for histochemistry were obtained by dissection of fresh cadavers. Tissues for electron microscopy were fixed and processed by conventional mesns. Formalin-fixed cadaver specimens were subjected to a battery of tests for glycoconjugates.Results: The anterior lingual salivary glands are composed predominantly of mucous tubules (which come in two distinct sizes: large and small), seromucous demilunes, and rare seromucous acini. Regardless of tubule size, mucous cells are typically in appearance and, like mucous cells in other human salivary glands, contain filamentous bodies. Histochemically, the larger tubules contain neutral glycoproteins, low concentrations of sialoglycoproteins, and large amounts of sulfated glycoproteins. The small mucous tubules contain neutral glycoproteins, much sialoglycoprotein, and relatively small amounts of sulfated glycoprotein. The seromucous cells, whether demilunar or acinar, are identical. They contain numerous secretory granules, which show a spectrum of internal patterns from one individual to another. These cells have considerable concentrations of neutral- and sialoglycoproteins and lower concentrations of sulfated gly-coproteins. Countrary to previously published reports, we could find no differences in the ratio of mucous to seromucous cells along the anteriorposterior lingual axis: there was no gradient of seromucous cells in our specimens. The ducts in the anterior lingual salivary glands are not precise counterparts of those in the major salivary glands, since the former have no capsules, hence lack lobulation. Without these familiar structural landmarks, the only duct that can be identified with certainty is the intercalated duct, and then only if it is in continuity with or lies close to a secretory endpiece. Such ducts consist of simple cuboidal epithelium of prosaic appearance. The ductular epithelium gradually thickens and gives rise to what appear to be excretory ducts consisting of columnar cells with few mitochondria. Scattered within the walls of the walls of the larger ducts are patches of typical striated ducts wherein the taller cells display basal striations resulting from highly folded basal plasma membranes and numerous, vertically oriented, virgulate mitochondria. In other atypical regions of the excretory duct, basal cells may have a primary cilium that juts into the intercellular space.Conclusions: There is a high degree of structural variability in human anterior lingual salivary glands. Because of the technical difficulties in collecting pristine saliva from these glands, the precise functions(s) of these organs remains unknown. © 1994 Wiley-Liss, Inc.
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    The @Anatomical Record 240 (1994), S. 178-188 
    ISSN: 0003-276X
    Keywords: Accessory submandibular gland ; Salivary gland ; Mucous droplets ; Gogli apparatus ; Secretion ; Exocytosis ; Bats ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Certain species of bats possess two sets of submandibular glands, namely, principal and accessory. The ultrastructure and histochemistry of the accessory submandibular gland was examined in three species of long-winged bats.Methods: Specimens of Miniopterus schreibersi and M. Magnator were live-trapped in Thailand, and of M. inflatus were live-trapped in Kenya. For electron microscopy, accessory submandibular lands were initially fixed in triple aldehyde-DMSO, postfixed in osmium tetroxide, and embedded in Epon-Maraglas. A portion of the glands collected in Thailand (M. schreibersi and magnator) was fixed in buffered formalin and embedded in paraffin. Sections of the latter material were subjected to a battery of histochemical tests for glycoconjugates.Results: Although in all three species the accessory submandibular glands have normal histological structure, the glands in two, M. schreibersi and M. magnator, were distinguished by possessing mucous droplets of unusual morphology. These droplets, whose identity as mucous was confirmed by histochemical tests for glygoconjugates, are delimited by maniflod membranes: up to 10 in M. Schreibersi and fewer, but still multiple, in M. magnator. In both species, the entire array of surface membranes may fold inward in the fashion of mitochondiral cristae, forming packets of membranes, many of which have the spurious appearance of floating free in the droplet matirix. These multipartite limiting membranes appear to originate simply by Golgi saccules and moderately large, flattened Golgi vesicles repeatedly wrapping themselves around the surface of nascent mucous droplets. During exocytosis, the outermost membrane of each mucous droplet contacts the luminal membrane, this barrie ruptures, then the remainder of the droplet - multiple membranes and matrix - either flow into the lumen or are cast out in toto. In either case, a great deal of membrane phospholipid is added to the salivea. This salivary lipid may permit these bats to consume insects that normally are able to repel predators with chemical defenses that make them unpalatable. The thrid species that we studied, M. inflatus, has mucous droplets of normal appearance, i.e., they have only one limiting membrane.Conclusions: The varying structure of mucous secretory products among the species of Miniopterus provides important clues as to the evolution of this genus as well as to the evolution of secretory cells in general. © 1994 Wiley-Liss, Inc.
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  • 159
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    The @Anatomical Record 240 (1994), S. 507-515 
    ISSN: 0003-276X
    Keywords: Muscle spindles ; Chicken leg muscles ; Intrafusal fiber types ; Slow myosins ; Fast myosins ; Coexpression ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Chicken intrafusal fibers were classifed on the basis of their myosin heavy chain (MHC) composition, which was compared to that of mammalian nuclear bag and nuclear chain types.Methods: Immunoreactivities of intrafusal fibers from leg muscles of 8-week-old chickens were evaluated in serial cross-sections after incubation with monoclonal antibodies against slow-twitch, slow-tonic, or fast-twitch MHC and fast muscle C-protein.Results: Four categories of slow intrafusal fiber could be distinguished on the basis of differential expression of slow-twitch and slow-tonic MHC. Segregation into types was most evident at the motor axon supplied pole, followed by the sensory region of the equator. Fiber types were least distinct at the juxtaequator where sensory and motor axons meet. Intrafusal fibers negative for slow myosins reacted with anti-fast myosins. Fast fibers were best viewed as a single group without subdivisions. Immunostaining for fast muscle C-protein paralleled in large part reactivities for neonatal/fast MHC, indicating that proteins other than MHC are useful fiber type markers.Conclusions: Despite regional changes along the length of intrafusal fibers and some variation within fiber types, the concept of separate MHC-based fiber types was valid as long as typing of fibers was restricted to the proximal polar region. Comparisons of MHC profiles revealed similarities between chicken fast intrafusal fibers and mammalian nuclear chain fibers and between some chicken slow intrafusal fibers and mammalian nuclear bag fibers. © 1994 Wiley-Liss, Inc.
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  • 160
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    The @Anatomical Record 240 (1994), S. 528-536 
    ISSN: 0003-276X
    Keywords: Beta-endorphin ; Oxytocin ; Pituitary gland ; Hypophysis ; Adenohypophysis ; Neurohypophysis ; Immunohistochemistry ; Bos taurus ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Beta-endorphin and oxytocin immunocytochemical localization were examined in the neurointermediate lobe (lobus nervosus and pars intermedia) of the bovine hypophysis in order to describe the anatomical distribution of these two neurointermediate lobe hormones.Methods: Twenty-seven bovine hypophyses were collected from slaughterhouse animals (seven mature lactating cows, eleven mature nonlactating cows, three nulliparous heifers, and six steers). Hypophyses were immunostained for oxytocin-containing fibers and β-endorphin-secreting cells by using the avidin biotin-immunoperoxidase method. The distributions of β-endorphin-positive cells and oxytocin-positive nerve fibers were plotted on projected outlines of the hypophyses. Immunoreactive staining intensity was graded numerically as weak, moderate, or heavy by three individuals who had no knowledge of the animals' physiological status.Results: Oxytocin immunoreactivity was confined to the lobus nervosus while β-endorphin staining was confined to the pars intermedia and the pars distalis. However, oxytocin immunopositive neurosecretory terminals were distributed more heavily in that part of the lobus nervosus bordering the pars intermedia than in the center of the lobe.Conclusions: These results were similar to those previously reported for the rat (Swaab et al., 1975; J. Neural Transm., 36:195-215; Deftos and Catherwood, 1980; Life Sci., 27:223-228). © 1994 Wiley-Liss, Inc.
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  • 161
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    The @Anatomical Record 240 (1994), S. 537-544 
    ISSN: 0003-276X
    Keywords: Lectins ; Sheep ; Preimplantation embryo ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Preimplantation development of mammalia is characterized by cell surface changes functioning in intercellular communication and adhesion. The glycoconjugate role in cellular interactions has been analysed for several groups but not in sheep embryos. The binding patterns of eleven lectins during sheep preimplanatation development were investigated and the role of glycoconjugates in early development was discussed.Methods: Ultrathin sections from preimplantation ovine embryos (3-7 days) were incubated with different colloidal gold conjugated lectins and the frequency of gold particles on the cell membrane, some organelles, and the zona pellucida was evaluated.Results and Conclusions: We observed a higher staining of WGA, DBA, and SBA lectins in the intercellular contact zone with respect to the free cell surface of blastomeres during cleavage. This indicates that the N-acetyl galactosamine and N-acetyl glucosamine residues may be involved in sheep morula compaction. In contrast, the trophoblast cell displays an increase of staining of some lectins previously identified during cleavage (LcH, WGA, SBA, MPA, and PNA) on the free membrane, and a lack of sugar residues in the intercellular surface. This polarization of the trophoblast cell surface is not observed in the inner cell mass and could provide a mechanism for differentiation within the blastocyst. Intracytoplasmic vesicles show a cytochemical identity with lysosomes in the blastocyst (abundant GlcNAc and Man/Glc residues) that may reflect a functional relationship between both organelles in an intracellular cycle. The zona pellucida presents abundant GalNAc, GlcNAc, and Gal residues during preimplantation ovine development. © 1994 Wiley-Liss, Inc.
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  • 162
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    The @Anatomical Record 240 (1994), S. 516-527 
    ISSN: 0003-276X
    Keywords: Spermatozoa ; Actin ; 53 kDa protein ; Immunocytochemistry ; Rat ; Mouse ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Presence of immunocytochemically detectable actin in the rat and mouse sperm head has been enigmatic for years. In this study, we demonstrate actin in the perinuclear theca and show that the detection of actin epitopes in the rat and mouse epididymal spermatozoa can effectively be enhanced by pre-extraction of sperm cells with SDS.Methods: The study with one monoclonal and one polyclonal anti-actin antibody was carried out at conventional and confocal fluorescence and electron microscope level, and by immunoblotting of proteins isolated from the head and tail fractions.Results: In the head of the control methanol-acetone fixed rat spermatozoa, the polyclonal antibody gave a stronger immunostaining in the postacrosomal area and in the perforatorium than the monoclonal antibody. In the mouse sperm head, the monoclonal antibody labeled the ventral edge of the postacrosomal area and slightly the perforatorium, whereas the polyclonal antibody stained the entire perinuclear space. In the SDS-extracted spermatozoa, an intense postacrosomal and perforatorial labeling was obtained with both antibodies but, in particular in the rat spermatozoa, the middle lateral portion of the postacrosomal segment remained unlabeled. Sonication seemed to cause structural modifications which specifically impeded staining with the monoclonal antibody. Both antibodies detected actin in the basal plate and the monoclonal antibody in the neck. Amorphous matrix of the connecting piece showed immunogold labeling. In the tail, the monoclonal antibody recognized actin and a relatively basic 53 kDa polypeptide, whereas the polyclonal antibody reacted with several protein bands. SDS-soluble actin of the tail was addressed to the midpiece and the SDS-insoluble 53 kDa protein profoundly to the outer dense fibers of the principal piece.Conclusions: Intense labeling of actin in the SDS-extracted rat and mouse spermatozoa was presumably due to the generated demasking of actin epitopes embedded in the perinuclear cytoplasm. The results are important in confirming that actin in the rat and mouse sperm head is not lost during spermiogenesis but apparently contributes to the three-dimensional packing of the mature perinuclear cytoplasm. This study further demonstrates the importance of the methods used in sample preparation and advantages of conofocal microscopy when attempting to detect cytoskeletal proteins which, as in spermatozoa, may occur in small quantities. © 1994 Wiley-Liss, Inc.
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  • 163
    ISSN: 0003-276X
    Keywords: Alveolar-like structures (ALS) ; Fetal lung cell maturation ; Lung maturation in vitro ; Type II cell differentiation ; Undifferentiated lung cells ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Formation of alveolar-like structures (ALS) by mature fetal rabbit type II pneumocytes (day 29 gestation) and long-term differentiation on Engelbreth-Holms-Swarm mouse tumor extract or EHS gel (Matrigel) were reported by our group (Blau et al., 1988. J. Cell Physiol., 136:203-214). We now describe structural organization and differentiation of immature lung epithelial cells, isolated at day 22 gestation, into mature type II cells in vitro.Methods: Peripheral pulmonary tissue was pooled and undifferentiated epithelial cells isolated for primary culture on Matrigel. Cells were examined 12-16 h after plating and on days 1,3,5, and 7 of culture and assessed by phase contrast and by transmission electron microscopy after fixation in situ.Results: Cells formed ALS 12-16 h after plating. Spherule diameter increased about four to eight times from day 1-7 in culture. There was rapid transformation of tall columnar cells to cuboidal, normal polarization of cells with respect to cell-free lumen of ALS, progressive reduction of glycogen zones, apparent gradual increase of cell organelles such as Golgi apparatus, rough endoplasmic reticulum and mitochondria, and apparent extrusion of lipidic figures into the lumen. These morphologic transformations in vitro temporally paralleled cell differentiation in vivo. The relative increase of 14C-acetate precursor into phosphatidylcholine in contrast to cardiolipin was consistent with these transformations.Conclusions: Under the conditions of our culture system, maturation of undifferentiated pulmonary epithelial cells is reproduced in vitro along the same time course and according to the same developmental sequence of fetal lungs in vivo. © 1994 Wiley-Liss, Inc.
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  • 164
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    The @Anatomical Record 239 (1994), S. 177-184 
    ISSN: 0003-276X
    Keywords: Immunogold electron microscopy ; GH cell ; Anterior pituitary gland ; Normal human fetus ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Ultrastructural studies of growth hormoneproducing cells (GH cells) in the anterior pituitary gland have been reported using several experimental animals. However, no attempt has yet been made to identify the ultrastructural heterogeneity of the GH cells within the human anterior pituitary gland. To this end, we employed immunogold electron microscopy to investigate the ultrastructural characteristics of GH cells in relation to gestational age in normal human fetuses.Materials: Based on ultrastructural characteristics, three distinct types of GH cells were identified by immunogold electron microscopy in the anterior pituitary glands of 34 normal human fetal pituitary glands. The age of the tissue samples ranged from 8 to 34 weeks.Results: The Type-I GH cell is a small, round cell with a narrow cytoplasm containing a few small secretory granules (268 nm in mean diameter). The GH cells designated Type-II are polygonal and contain medium-sized secretory granules (347 nm), profiles of rough endoplasmic reticulum (RER) arranged in parallel lamellae, and a Golgi complex which is frequently encountered but only in this cell type. The Type-III GH cell is polygonal, large, and contains numerous large spherical-shaped secretory granules (404 nm). The Type-I was the predominant cell type until about 20 weeks of gestation; its incidence decreased thereafter. In contrast, the Type-II and Type-III cells increased in number starting at 20 weeks of gestational age.Conclusion: From these results, we suggest that Type-I is the most immature type of GH cell, Type-III the most mature, and the Type-II is intermediate in development. The marked difference in the incidence of each GH cell type between the first and second half of gestation appears to be a reflection of the development of the hypothalamic regulation of the anterior pituitary gland, which is reported to be established at around 20 weeks of gestation. © 1994 Wiley-Liss, Inc.
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  • 165
    ISSN: 0003-276X
    Keywords: Development ; Immunohistochemistry ; Renin-containing cells ; Sheep ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Renin-containing (RC) cells in small ruminant kidneys have been known to be widely distributed along the blood vessels. In the present study, RC cells in developing sheep kidneys were studied to investigate not only the appearance but distribution with the potential physiological significance using immunohistochemical and histophanimetrical techniques.Methods: Seven fetal, 12 newborn, and 3 adult metanephric kidneys were used and immunostained by anti-renin antiserum. In the histoplanimetrical analysis, the numerical values of RC cells existing at the walls of 3 major arterial types in the kidneys were calculated.Results: At day 44 of gestation, RC cells were already demonstrated in the walls of renal, interlobar, and afferent vessels, located in the deep cortex and the medulla. In intermediate gestational periods, RC cells were detected throughout the intrarenal arterial trees. In late gestational periods, RC cells expressed in the walls of interlobar/arcuate and interlobular arteries tended to decrease or disappear gradually, while they were distributed predominantly in the afferent glomerular vessels. In newborn lambs, especially days 1 to 3 after birth, increased numbers of RC cells were demonstrated throughout the arterial trees in the kidneys. In older lambs, RC cells located in the interlobar/arcuate arteries and the proximal region of the interlobular arteries decreased in number and gradually disappeared. Some RC cells were still distributed in the distal portion of the interlobular artery even in the adult sheep.Conclusions: These results suggest that the wide distribution of RC cells in sheep kidney is formed in perinatal life, and that the neuronal regulation is associated with the maintenance of this distribution. © 1994 Wiley-Liss, Inc.
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    The @Anatomical Record 239 (1994), S. 198-215 
    ISSN: 0003-276X
    Keywords: Deer ; Pedicle ; Antler ; Intramembranous ossification ; Endochondral ossification ; Antlerogenic periosteum ; Perichondrium ; Transitional ossification ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Although it is known that deer antlerogenic potential resides in the periosteum of an antlerogenic region and antler forms through modified endochondral ossification, how a deciduous antler forms histologically through a permanent pedicle from the periosteum has not been reported.Methods: Histogenesis of the pedicle and the early first antler in red deer was systematically examined using light microscopy techniques.Results and Conclusions: At the pre-pedicle stage, the frontal lateral crest (under 5 mm in height) consisted horizontally of antlerogenic periosteum and underlying cancellous bone. Both the cellular layer (3.74 times, P〈0.01) and the fibrous layer of the antlerogenic periosteum were much thicker than those of the margin of the antlerogenic region or the facial periosteum. The crest was formed through intramembranous ossification. When the pedicle began to develop (5-15 mm in height), some discrete clusters of mature chondrocytes appeared in the bony trabeculae, which signified the beginning of the transition of the ossification pattern from the intramem branous to the endochondral. The pedicle consisted of three portions from distal to proximal, periosteum/perichondrium, osseocartilaginous tissue, and osseous tissue. When the pedicle became visible (about 20 mm in height), it consisted of the same three portions as the pedicle initiation stage, but the osseocartilaginous portion was expanded compared to the initiation stage and the cartilaginous proportion increased distally. When the pedicle grew to 25-40 mm in height, continous cartilaginous trabeculae appeared under the apical perichondrium. The pedicle consisted of four portions from distal to proximal: perichondrium, cartilaginous tissue, osseocartilaginous tissue, osseous tissue. It was formed through endochondral ossification. All these ossification pattern changes could not be seen externally as the overlying integument was characterised by typical scalp skin. When the pedicle grew to about 60 mm in height, antler tissue was visually apparent at the apex as the hair type changed from scalp hair to the velvet-like hair of growing antler. However, this transformation could not be distinguished internally as the inside tissues were all continuous between pedicle and antler. Therefore, the histogenesis of the deer pedicle and the first antler originated from the antlerogenic cells and covered two phases: an internal phase through which pedicle was formed and an external phase which signalled the beginning of antlerogenesis. © 1994 Wiley-Liss, Inc.
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    The @Anatomical Record 239 (1994), S. 230-230 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 168
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    The @Anatomical Record 239 (1994) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 169
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    The @Anatomical Record 239 (1994), S. 216-223 
    ISSN: 0003-276X
    Keywords: Scanning electron microscopy ; Myocardium ; Atrioventricular valves ; Embryology ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Before septation the entire atrioventricular canal is connected with the ventricular inlet segment (primitive left ventricle), wheres the mature heart exhibits an exclusive connection of the right atrium to the right ventricule. The process which is responsible for this change is controversial.Methods: Graphic reconstructions of serially sectioned embryonic rat hearts as well as scanning electron micrographs of similar specimens were made.Results: The first indication of a right atrioventricular connection was seen as a groove in the atrioventricular junctional myocardium to the right of the inferior endocardial cushion. This groove expanded to form the right ventricular inlet portion. The right, inferior, and superior walls of this newly formed cavity were formed from junctional myocardium, which demarcated it from the trabeculated right ventricular portion in all developmental stages. The left wall equally developed from this junctional myocardium and formed the ventricular inlet septum. The junctional myocardium between right ventricular inlet and trabeculated portions was seen to develop into the tricuspid valve and its tension apparatus.Conclusions: The preseptation embryonic heart has no inlet portion to the right ventricle. This new cavity is created by remodelling of atrioventricular junctional myocardium. This myocardium also provides the material contribution to the tricuspid valve and its tension apparatus. Malformations of the right ventricular inlet portion and of the tricuspid valve are indissolubly linked. © 1994 Wiley-Liss, Inc.
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  • 170
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    The @Anatomical Record 239 (1994), S. 224-229 
    ISSN: 0003-276X
    Keywords: Cleft palate ; Diprosopic ; Dipygus ; Gonadal dysgenesis ; Porcine ; Swine-abnormalities ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Twins with doubliong of the cranial and crudal poles, yet having a single thorax, are rare.Methods: One set of diprosopus, dipygus porcine conjoined twins was studied.Results: In addition to the conjoining anomaly, these twins also exhibited ambiguous internal reproductive features. The twins had two snouts, three eyes, a single thorax, and were duplicated from the umbilicus caudally. Radiography indicated a single vertebral column in the cervical region. The vertebral columns were separate caudally from this point. There was a total of six limbs - one pair of forelimbs and two pairs of hindlimbs. Many medial structures failed to develop in these twins. Medial cranial nerves V-XII were absent or displaced although apprarently normal laterally. The medial palates were present but shortened, whereas the medial mandibular rami had folded back on themselves rostrally to form a midline mass between the two chins. Each twin had only one lateral kidney and one lateral tests. Medial scrotal sacs were present but devoid of a testis. There was a midline, “uterine”-like structure which crossed between the twins. However, histological analysis of this structure revealed it to be dysplastic testicular tissue.Conclusions: The relationship between the abnormal reproductive features in these twins and the conjoining is unclear. The anatomy of these twins, in addition to the literature reviewed, illustrates the internal anatomical heterogeneity of grossly similar conjoined twins. A review of the literature also suggests that conjoined twinning may be more common in swine than was previously suspected. © 1994 Wiley-Liss, Inc.
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    The @Anatomical Record 239 (1994), S. 231-242 
    ISSN: 0003-276X
    Keywords: Cell lines ; Endothelium ; Gravin ; Immunohistochemistry ; Mice ; Rabbits ; Papio ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Gravin, a novel, high molecular weight, intra-cellular protein, is expressed in endothelial cells and several other adherent cell types in vitro. To gain insights into its function, we examined the distribution of gravin in tissues.Methods: Affinity-purified polyclonal and monoclonal antibodies were raised against a bacterial fusion protein corresponding to the carboxyl terminus of gravin and against affinity-isolated gravin. The specificity of the antibodies was characterized by immunoblotting bacterial, cell, and tissue extracts. The characterized antibodies were used to localize gravin in baboon tissue sections by immunocytochemistry and immunofluorescence microscopy.Results: The antibodies specifically immunoblotted the fusion protein and recognized either a band at 250 kDa or a doublet at 300 kDa on immunoblots of MG63 cells, HEL cells stimulated with phorbol ester, and several baboon tissues. In tissue sections, cell types that express gravin included fibroblasts, components of the peripheral and central nervous system, the adrenal medulla, the somatic layer of Bowman's capsule, cells associated with the glomerulus, and smooth muscle of certain organs. In contrast, most epithelia and all endothelia, with the exception of endothelia of the hepatic sinusoids and intestinal lacteals, lacked gravin. Levels of gravin mRNA expression in stimulated HEL cells increased dramatically when cells were stimulated in the presence of cycloheximide, suggesting that gravin expression may be partly regulated by protein-dependent mRNA catabolism.Conclusions: These data indicate that gravin expression is regulated in endothelial cells, possibly through protein-dependent mRNA catabolism. The strong expression of gravin in fibroblasts, neurons, and cells derived from neural crest in vivo and in adherent cells in vitro further suggests that this protein may play role in the modulation of cell motility and adhesion. © 1994 Wiley-Liss, Inc.
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  • 172
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    The @Anatomical Record 239 (1994), S. 243-254 
    ISSN: 0003-276X
    Keywords: Bone ; Ovariectomy ; Immobilization ; Bone resorption ; Bone formation ; Rats ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Ovariectomy (OVX) and immobilization (IMM) in rats are useful models of osteopenia, replicating some aspects of osteoporosis in humans. The purpose of this study was to compare changes in cancellous bone after OVX and/or IMM.Methods: Differences in cancellous bone were determined at 6 and 12 weeks after OVX or IMM. Comparisons were also made when rats were ovariectomized or immobilized for 6 weeks and then immobilized (OVX/IMM) and ovariectomized (IMM/OVX), respectively, for 6 more weeks. The femurs were used to determine bone mineral content (BMC) using single photon absorptiometry (SPA) and for scanning electron microscopy (SEM). Tibias were collected for microradiography, image analysis, and histomorphometry of metaphyseal cancellous bone.Results: Six and 12 weeks after OVX, there was less cancellous bone mass, compared with controls, as indicated by SPA, SEM, microradiography, image analyses, and histomorphometry. Bone was lost primarily from the central metaphyseal regions in the OVX animals, whereas the loss occurred throughout the metaphyses in the IMM animals. There were more rodlike bone spicules and fewer platelike trabecule in the OVX and IMM groups compared with controls. Differences in the structural aspects of the cancellous bone, including differences in the types of bone struts and marrow star volumes, indicated less trabecular connectivity and greater trabecular separation in the OVX and IMM animals, compared with controls. Endochondral growth indices in the IMM groups tended to be less, whereas the OVX groups tended to be greater than controls. Cancellous bone formation rates were generally greater in the OVX groups but less in the IMM groups compared with controls. Osteoclastic resorption surfaces were substantially elevated in the IMM and OVX groups, particularly the IMM groups. Changes reflecting OVX and IMM, independently, were apparent in the OVX/IMM and IMM/OVX groups and indices of osteopenia were different from controls, including less bone mass, trabecular connectivity, and greater trabecular separation, bone turnover rates, and osteoclastic surface.Conclusions: These results demonstrate differences in the osteopenic changes that occur in cancellous bone following OVX or IMM. The changes were generally more dramatic in the IMM than in the OVX animals. When OVX and IMM were applied in combination, the osteopenic changes are particularly severe, emphasizing the importance of mechanical usage even with a deficiency of gonadal hormones. © 1994 Wiley-Liss, Inc.
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  • 173
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    The @Anatomical Record 238 (1994), S. 374-382 
    ISSN: 0003-276X
    Keywords: Tendon of Todaro ; Development ; Human embryos ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: This study covers the development of Todaro's tendon during human embryonic and fetal periods. The tendon primordium first appears when human embryos attain a CR length of 22 mm, but it only becomes well-defined at 24 mm CR length. The tissue that will form the tendon proceeds exclusively from the inferior endocardial cushion. The tendon establishes a close relationship with the base of the septum secundum during its path towards the right venous valve, carrying myocardial tissue out and forming the fasciculus limbicus inferior to muscular tissue. The tendon's relationship with the superior aspect of the atrioventricular node primordium during the first part of its path is of particular interest. The relationship is most intriguing when the node morphology is least defined. This would explain the possible embryogenesis of extra atrioventricular nodes. We also consider Todaro's tendon to be largely responsible for the development of the sinus band which protrudes as a crest inside the right atrium. This band is particularly well-developed in the fetal heart and provides an explanation for the large sub-Eustachian sinus cavity. © 1994 Wiley-Liss, Inc.
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  • 174
    ISSN: 0003-276X
    Keywords: Tooth development ; Mouse ; Protein translocation ; Amelogenin ; Epithelial-mesenchymal interactions ; Intercellular communication ; Immunocytochemistry ; Differential gene expression ; In vitro organ culture ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The developmental problem of how dental epithelia and/or dental papilla ectomesenchyme induce and/or up- or down-regulate tooth formation are as yet unresolved issues. We have desinged studies to map the synthesis and fate pathways of secreted amelogenin proteins from Kallenbach differentiation zones II-IV during in vivo and in vitro mouse mandibular first molar tooth development (M1). Tooth organs from cap, bell, and crown stages were processed for reverse transcriptase/polymerase chain reaction (RT-PCR) and high resolution Protein A immunocytochemistry using anti-amelogenin and anti-peptide antibodies. Cap stage M1 were cultured for periods ranging from 10-21 days in vitro using either serumless, or 15% fetal calf sera-supplemented, chemically-defined medium. Amelogenin transcripts are expressed in the mouse embryonic molar from E15 through early postnatal development. Amelogenin antigens were first detected in Kallenbach's differentiation zone II. Amelogenin proteins secreted from preameloblasts were identified along cell processes and cell surfaces of odontoblasts adjacent to forming mantle dentine extracellular matrix (ECM) prior to biomineralization. Amelogenin proteins were restricted to forming endocytotic vesicles, clathrin-coated vesicles, and lysozomes within odontoblasts. At later stages (e.g. 2 days postnatal development), enamel proteins were not identified in odontoblasts or predentine matrix following mineralization. Comparable observations for stages of development were noted for in vitro cultured tooth explants. Preameloblasts synthesize and secrete amelogenin proteins which bind to odontoblast cell surfaces possibly through the process of receptor-mediated endocytosis. We conclude that amelogenin proteins secreted from preameloblasts, prior to the initiation of biomineralization, were translocated to odontoblasts to serve as yet unknown biological functions. © 1994 Wiley-Liss, Inc.
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  • 175
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    The @Anatomical Record 238 (1994), S. 397-406 
    ISSN: 0003-276X
    Keywords: Chick embryo ; Development TGFβ ; Immunocytochemistry ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: We have used an antibody against a TGFβ peptide fragment to localize this growth factor in the early chick embryo from laying to the ten-somite stage of development. Western blotting showed that the antibody reacted with both mammalian TGFβ1 and chicken TGFβ3. By immunocytochemistry we find that at the earliest developmental stage (stage X of Eyal-Giladi and Kochav) immunoreactivity to this antibody is primarily located in the cells of the area opaca and marginal zone, as well as in the most peripheral edge cells of the blastoderm. The yolk is non-reactive, except in a highly localized region subjacent to the edge cells. This pattern persists at stage XII, and at both stages individual isolated cells in the epiblast and hypoblast are also reactive. By the time to gastrulation, reactivity in the epiblast is polarized to the ventral extremity of the cells, and again some isolated cells in this layer are intensely immunoreactive. At this stage also, the endoderm cells, particularly those underlying the primitive streak, are positive, as are the mesoderm cells lateral to the streak. At somite stages, the neuroepithelium is not reactive but the ectoderm lateral to it is strongly positive. At the caudal primitive streak levels of early somite embryos, the ectoderm and endoderm are immunoreactive while the mesoderm loses the reactivity it showed at the early gastrulation stages. The neuroepithelial cells later show reactivity at their apical poles, and, as at the earlier stages, individual cells show intense labelling. These results indicate that TGFβ1 and/or TGFβ3 immunoreactivity is developmentally regulated from very early stages of morphogenesis in the chick, and together with data from earlier functional studies, suggest that this factor has roles in embryonic axis formation and in blastoderm expansion. © 1994 Wiley-Liss, Inc.
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  • 176
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    The @Anatomical Record 238 (1994), S. 424-424 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 177
    ISSN: 0003-276X
    Keywords: Respiratory Biology ; Pulmonary hypoplasia ; Lung pathology ; Chondrodystrophy ; Mouse ; Embryo/fetus ; Ultrastructure ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Fetal mice homozygous for the Disproportionate micromelia (Dmm) gene were studied as a model for pulmonary hypoplasia in chondrodystrophy.Methods: Wet weight, dry weight, and biochemical content were determined in excised whole lungs, terminal sac morphology and presence of multilamellar bodies were determined by electron microscopy, and volume of the thoracic space was estimated from paraffin casts. Lung development of the mutant was further assessed in whole organ culture.Results. Compared with normal littermates, the mutant showed a significant decrease (28%) in lung wet weight without showing altered lung dry weight or tissue content of DNA and protein. The terminal sacs of lungs fixed by intratracheal instillation were significantly smaller than normal. However, the lungs appeared to have undergone maturation on schedule since the surfactant precursors, multilamellar bodies, were observed and normal tissue-levels of phospholipid were detected. The volume of the mutant's thorax was markedly reduced. Finally, the mutant's lungs when removed from the fetus prior to the onset of thoracic dystrophy (day 15) and cultured for three days demonstrated that, without the confining influence of a reduced thoracic space, they are capable of development comparable to normal.Conclusions: These findings support the hypothesis that the Dmm mutant can be further studied as a model for human pulmonary hypoplasia associated with chondrodystrophy, and that the relationship between the reduced thorax and the lung disorder is cause-and-effect. © 1994 Wiley-Liss, Inc.
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  • 178
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    The @Anatomical Record 238 (1994), S. 199-206 
    ISSN: 0003-276X
    Keywords: Cardiac myocyte ; Mitochondria ; Morphometry ; Volume density ; Rat ; Rabbit ; Guinea pig ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The ultrastructural quantitative composition of left ventricular cardiac myocytes from isolated Langendorff-perfused hearts was studied in three different mammals (rabbit, guinea pig, and rat). Volume densities of mitochondria, myofibrils, and unspecified cytoplasm were determined using morphometry and were compared to functional parameters including left ventricular developed pressure (LVDP), contractility (dP/dt), heart rate, TTI (tension-time index, an index of oxygen consumption), and relative heart mass (H/B) obtained from these hearts. Each of the mammals was found to possess a very specific and characteristic quantitative composition of cardiac myocyte. Cardiac myocytes contained 26.8% mitochondria and 56.3% myofibrils in rabbits, 25.8% mitochondria and 60.9% myofibrils in guinea pigs, and 27.7% mitochondria and 58.1% myofibrils in rats. The LVDP, contractility, heart rate, and TTI were quite different among species. However, there were close correlations between the mitochondrial volume density and the LVDP (p 〈 0.05), and between the mitochondrial volume density and the TTI (p 〈 0.05), in any group of the animals. It is concluded that the mitochondrial volume density is a good indirect indicator of function of cardiac muscle related to oxidative capacity. © 1994 Wiley-Liss, Inc.
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  • 179
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    The @Anatomical Record 238 (1994), S. 207-212 
    ISSN: 0003-276X
    Keywords: Calbindin-D28k ; Calmodulin ; Calretinin ; Chickens ; Glial cells ; Immunohistochemistry ; Melatonin synthesis ; Pinealocytes ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Calmodulin distribution in the chicken pineal organ was investigated by immunohistochemistry. Calmodulin immunoreactivity was detected in ependymocytes in the follicular zone and in interstitial cells in the parafollicular zone. No calmodulin immunoreactivity was detected in pinealocytes. Lack of calmodulin immunoreactivity in pinealocytes raises questions about its proposed function in melatonin synthesis as suggested by pharmacological studies using calmodulin antagonists. The calmodulin distribution was comparable to that of S100, a glial cell marker. Two other markers, calbindin-D28k and calretinin, which in neuroanatomical studies give excellent cytoarchitectonic staining, in the chick pineal permitted the detection of two subclasses of pinealocytes. One was darkly stained by calbindin-D28k and rare. The other was very abundant and calretinin positive. In the parafollicular zone, calbindin-D28k and/or calretinin antibodies allowed us to visualize cells presenting a neuron-like morphology. Calretinin immunoreactivity was detected in nearly all pinealocytes in which hydroxy-indol-O-methyl transferase was also located. Comparison between the lack of calmodulin and the presence of calretinin, belonging to the same calcium-binding protein family, in chick pinealocytes raises the hypothesis about a possible role of calretinin in melatonin synthesis. © 1994 Wiley-Liss, Inc.
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  • 180
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    The @Anatomical Record 238 (1994), S. 213-224 
    ISSN: 0003-276X
    Keywords: Lymph node ; Innervation ; Immunostimulation ; Silver impregnation ; Ultrastructure ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The purpose of this investigation was to test the hypothesis that activation of the immune system in rats will lead to changes in the density of innervation in lymph nodes. In order to reduce the variability between animals, the rats were reared under sterile conditions and immunostimulation was effected by subcutaneous application of bovine albumin in a region draining to the axillary lymph nodes of both sides. Control animals received an equivalent application of sterile physiological saline. The animals were sacrificed 10 days and 27 days and 4 months after immunostimulation. The nerves in the axillary lymph nodes were quantified by light microscopy in silver impregnated sections and at the ultrastructural level on ultrathin sections. The survival times were chosen so that the first group was in the ascending phase of antibody production, the second group at the peak, and the third group in the declining phase. Both at the light and ultrastructural levels, there were statistically significant differences in the density of innervation of medulla between the groups, with a particularly pronounced increase in the group 4 months after immunostimulation. At the ultrastructural level, there was also an increase in the density of incompletely ensheathed axonal profiles in the parenchyma of the medulla, while the nerves associated with blood vessels were not increased. We conclude that immunostimulation leads to morphological changes in the innervation of the medulla of axillary lymph nodes, that are consistent with the concept of functional activation of the autonomic nervous system through the immune system. © 1994 Wiley-Liss, Inc.
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  • 181
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    The @Anatomical Record 238 (1994), S. 225-236 
    ISSN: 0003-276X
    Keywords: Chick embryo ; Amnion ; Ectoderm ; Epithelium ; Morphogenesis ; Autoradiography ; Growth ; Cell cycle ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Patterns of cell proliferation in ectoderm epithelium that will form avian amnion correlate with morphogenesis, but not in an obvious pattern with respect to large-scale folding. At sites where the pre-axial amnion folds will first appear in 4- to 8-somite embryos, patterns of proliferation do not separate into domains that presage location of the single pre-axial fold that is commonly described in embryology texts. Instead, increased cell proliferation occurs in a significant, bilateral pattern. In stages with 13 to 27 somites, when lateral amnionic folds are prominent, five paraxial domains of cell proliferation correlate with morphology and show decreasing levels of cell proliferation with distance from the neural axis. Slowly growing areas surround rapidly growing areas and could assist buckling of epithelium by providing constraint on expansion of faster growing areas. Proliferation domains in ectoderm correlate with morphology and morphological events when localized changes in cell shape are lacking and suggest a role for differential cell proliferation in formation of large-scale epithelial folds in early chick embryos. © 1994 Wiley-Liss, Inc.
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  • 182
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    The @Anatomical Record 238 (1994), S. 237-247 
    ISSN: 0003-276X
    Keywords: Embryonic development ; Esophagus ; Growth ; Trachea ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Esophageal atresia and tracheoesophageal fistula, common malformations of the respiratory and digestive tracts, are of unsettled pathogenesis. Part of the difficulty in understanding these abnormalities arises from the uncertainties about the normal developmental processes in the region. This study examined the development and fate of the tracheoesophageal septum. Normal human embryos from the Carnegie Embryological Collection and fetuses from the Hopkins Pathology Collection were examined, and reconstructions of selected specimens were made from photomicrographs of serial histologic sections. The results show that the lung bud appears in Carnegie stage 12, rapidly enlarges, and bend caudally, thereby producing a sulcus between the foregut and the respiratory system on its caudal aspect. The cranial aspect of this tracheoesophageal sulcus remains fixed at the levels of the first cervical vertebra throughout subsequent embryonic and fetal development. At the same time the trachea and esophagus elongate to bring those parts of the respiratory and digestive systems into their definitive anatomic positions. Examination of the tracheoesophageal sulcus shows that its growth-limiting properties may be explained by its catenoidal configuration. Catenoidal, or saddle-shape, sulci have been shown to have similar regional growth-limiting properties in the embryonic heart. These regions contrast with outwardly convex regions in both the developing heart and lung where growth of the tissues occurs. The observations made here suggest that the origin of the tracheoesophageal malformations must be sought in a configurational abnormality in the area of the developing lung bud in Carnegie stage 12. © 1994 Wiley-Liss, Inc.
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  • 183
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    The @Anatomical Record 238 (1994), S. 248-262 
    ISSN: 0003-276X
    Keywords: Rat ; Facial nucleus ; Axotomy ; Axon reaction ; GABA ; Electron microscopy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The facial nerve was unilaterally crushed at its exit from the stylomastoid foramen in three 3-month old male rats. After 10 days survival, before the regenerating axons had reinnervated their target muscles, the facial nucleus was examined to determine central patterns of response in material prepared to demonstrate the presence of GABA-like immunoreactivity with postembedding procedures using gold-labeled secondary antibody. The uninjured nucleus served as a control. In both control and injured nuclei, the GABAergic terminals synapse with all parts of the motor neurons, except the axon, and exhibit diverse morphologies. GABAergic axon terminals vary in their size and in the electron density of their axoplasm and the majority of the terminals contain pleomorphic vesicle profiles that display a range in their packing density and size. In both control and injured facial nuclei, only ∼40% of the axon terminal profiles with pleomorphic vesicles exhibit GABA immunoreactivity. A morphometric analysis of the synaptic vesicle profiles in the GABA-positive terminals reveals that following axotomy there is no change in the mean number of synaptic vesicle profiles per GABAergic terminal profile. However, the mean size of the synaptic vesicle profiles in these terminals shows an axotomy-induced 50% increase, without change in the shapes of the enlarged vesicle profiles. Also, the numerical density of gold particles associated with the GABA-positive terminals is consistently greater in the injured than the control axon terminals. In the control animals quantitative analysis of the relative distribution of all axon terminal profiles in the neuropil categorized by the shape of their vesicle profiles as round, pleomorphic, or flat is 57:37:6. Ten days after axotomy the ratio of these categories in the injured nucleus has shifted to 35:60:5. This study demonstrates that the functional state of a postsynaptic target can influence the morphology of vesicle profiles in presynaptic elements as well as patterns of its afferent input. © 1994 Wiley-Liss, Inc.
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  • 184
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    The @Anatomical Record 238 (1994), S. 277-286 
    ISSN: 0003-276X
    Keywords: Magnetic resonance imaging ; Brain stem ; Neuroanatomy ; Arnold-Chiari deformity ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: High field proton magnetic resonance (MR) imaging has been applied to depict the MR appearaance of the normal excised human cervicomedullary junction, based on which neuropathologic specimens can be described. More specifically, two normal cases and one case of Chiari deformity were imaged in the transverse, sagittal, and coronal dimensions using a 9.4 Tesla vertical bore magnet. The MR images of the normal specimens reveal most of the neuroanatomical microstructures described in literature. An accurate description of the Chiari deformity could be made by comparing the MR reference images with those of the pathologic specimen. All MR detected abnormalities were confirmed by histopathology, by which no additional lesions could be found. © 1994 Wiley-Liss, Inc.
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  • 185
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    The @Anatomical Record 238 (1994), S. 263-276 
    ISSN: 0003-276X
    Keywords: Tongue ; Surface ; Musculature ; Iguanidae ; Reptile ; S.E.M. ; Histology ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The anatomy of the hyo-lingual apparatus in the iguanid lizard Oplurus cuvieri has been studied by light microscopy and scanning electron microscopy. Four areas were observed on the dorsal lingual epithelium of the lizard. Tongue tips are covered with a smooth epithelium. Closely packed flattened and cylindriform papillae cover the foretongue. The surface of the midtongue bears an unpapillose epithelium. Short conical papillae are arranged on the two lateral posterior bundles of the tongue. At high magnification, microvilli and microridges are widely distributed over the surface of the papillae. The epithelium of the papillae is composed of cells filled with secretory granules. Each surface plays successive roles during food ingestion, intra-buccal transport, and swallowing. The mucous interpapillary spaces would serve the adherence between the tongue and the food, the smooth epithelium of the midtongue should facilitate movements of the prey toward the pharynx, and conical papillae of the hindtongue present a rough surface which should act on the prey during the swallowing phase. The intrinsic morphology of the tongue is rather similar to that previously described for iguanids, but fibers of M. verticalis encircles ventrally the lingual process. These fibers could act in tongue protrusion as previously suggested for agamids. The morphology and function of the extrinsic tongue musculature and the hyoid musculature, analysed by electrical stimulations, are similar to the previous descriptions in iguanids and agamids either for feeding or displaying functions. © 1994 Wiley-Liss, Inc.
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  • 186
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    The @Anatomical Record 238 (1994), S. 287-288 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 187
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    The @Anatomical Record 238 (1994) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 188
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    The @Anatomical Record 238 (1994), S. 297-303 
    ISSN: 0003-276X
    Keywords: Fibrous tissue ; Joint surface ; Tibia plateau ; Kangaroo ; Mammals ; Pressure absorption ; Joint mechanics ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The central part of the articular surface on the tibia plateau of Macropus agilis consists of fibrous cartilage of soft consistency and the fiber arrangement is macroscopically visible. The peripheral portions of the plateau are covered by hyaline cartilage but do not communicate with the hyaline articular surfaces of the femur, as they are covered by the menisci. The fibrous cartilage covering of the tibia plateau is a compliant or readily deformed pad that could serve the function of deforming enough under high joint loads to allow surrounding regions of the articular cartilage to share in carrying those loads, thereby magnifying the articular contact surface and decreasing the magnitude of the peak unit loads in the region of the fibrous tissue pad. This pressure-absorbing mechanism represents the evolutionary response to the higher articular stress resulting from kangaroo locomotion. © 1994 Wiley-Liss, Inc.
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  • 189
    ISSN: 0003-276X
    Keywords: Feulgen reaction ; Cell cycle ; Chromosomes ; Interphase ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The Feulgen reaction has been utilized to localize DNA in nuclei throughout the cycle of mouse duodenal crypt cells using Epon-embedded 1 μm thick sections. The observed changes indicate that the 12.3 h long mitotic cycle of these cells can be subdivided into eleven stages, seven of which take place during the interphase. Computer measurements of Feulgen-stained nuclei and previous radioautographic studies indicate that DNA synthesis begins during stage I and ends during stage IV. The staining pattern shows no distinctive feature in the nuclei of the 1.5 h long stage I. Thereafter, marked changes occur during the rest of the interphase - that is during the 6.3 h that precede karyokinesis and the 3.5 h that follow it. Thus, at stage II the background of the nuclei darkens; at stage III, there appear stained threads interpreted as densifying chromosomes and dots interpreted as chromomeres, both of which thicken from 0.2 to 0.4 μm; at stage IV they further thicken to about 0.5 μm and at stage V, to about 0.7 μm. At this stage, which approximately corresponds to prophase, the intensely stained, discrete dots are localized within the less intensely stained sausage-shaped threads. As the breakup of the nuclear envelope introduces stage VI, whose early part corresponds to prometaphase, the intensely stained dots become close to one another within the threads and eventually fuse. The staining of the threads thus intensifies, and, by the late part of the stage that corresponds to metaphase, they have become the homogeneously dense metaphase chromosomes. At stage VII, the anaphase chromosomes reach each pole where they associate into a compact mass. This mass remains solid at stage VIII but gradually dissociates during stages IX, X, and XI as chromosomes are disassembled. © 1994 Wiley-Liss, Inc.
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  • 190
    ISSN: 0003-276X
    Keywords: Secretion pathway ; Yeast cells ; Carrier vesicles ; Golgi apparatus ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: The secretory protein transit between cisternae of endoplasmic reticulum (ER) and Golgi elements is blocked when the yeast Saccharomyces cerevisiae sec21 mutant is shifted from the permissive (24°C) to a non-permissive (37°C) temperature, but 30-50 nm vesicles accumulate in the cytoplasm. At the semi-permissive temperature of 33°C there is no complete block but rather a slowdown of the protein transport between ER and Golgi. The purpose of the present investigation is to analyze the structural expression of these events.Methods: S. cerevisiae sec21 mutants were maintained for 90 min at semi-restrictive (33°C) or restrictive (37°C) temperatures and then progressively returned to 24°C. Following fixation in glutaraldehyde and a postfixation in potassium ferrocyanide reduced osmium, 0.08 to 0.2 μm thick sections were cut from Epon embedded yeasts. Using the thicker sections, stereopairs of electron microscope photographs were prepared and used to visualize the three-dimensional configuration of the organelles.Results: At permissive temperature, the Golgi elements appeared as isolated networks of membranous tubules dispersed throughout the cytoplasm. The diameter of these membranous tubules varied considerably from one Golgi element to another. Larger tubules showed at their intersections distensions with size and staining intensity comparable with that of the secretory granules seen at proximity of the Golgi networks or at the cell periphery. Small vesicles in the 30-50 nm size range were rarely if ever observed in cells grown at permissive temperature. Golgi networks and secretion granules were less conspicuous in mutant cells maintained at 33°C and completely disappeared at 37°C. In both cases, the main structural feature was the presence in the cytoplam of numerous small vesicles and of short membranous tubules with a diameter identical to that of the small vesicles. As soon as 5 minutes after shifting mutants from 33°C to 24°C, the small vesciles disappeared from the cytoplasm, while secretory granules were actively produced in extensively developed Golgi network. When mutants were returned from 37°C to 24°C, the disappearance of small vesicles was more progressive and concomitant with the progressive reconstruction of Golgi networks.Conclusions: It is thus postulated that, in the above mentioned conditions, the small vesicles of the sec21 mutant did not act as intermediate carriers between the endoplasmic reticulum and a pre-existing Golgi apparatus, but rather fused together to produce newly formed Golgi networks. © 1994 Wiley-Liss, Inc.
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  • 191
    ISSN: 0003-276X
    Keywords: Seotonin ; Regulatory peptides ; Bombesin ; Somatostatin ; Neuroepithelial endocrine cells ; Neuroepithelial bodies ; Lung ; Quail ; Birds ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Despite extensive knowledge of the neuroepithelial endocrine (NEE) system in the lungs of species of various vertebrate classes, data on avians are limited. The present investigation deals with the light-and electron-microscopical immunocytochemistry and morphology of pulmonary NEE cells in the quail, Coturnix coturnix. Light-microscopically, serotonin immunoreactivity was detected in numerous solitary and clustered NEE cells located in the cilio-mucous epithelium of primary and secondary bronchi in adult as well as in newly hatched quails. Only in newly hatched quails could a small number of bombesin- and somatostatin-like immunoreactive NEE cells be demonstrated. Electron-microscopical morphology revealed that NEE cells contained dense-cored vesicles of a wide range of diameters and electron densities. Nearly all of the NEE cells were seen to rest on the basement membrane of the cilio-mucous epithelium, lacking direct contact with the luminal surface. Nerve varicostities or nerve endings, of both afferent and efferent morphological appearance, were found directly apposed to the basal portion of NEE cells, invaginating between NEE cells or between NEE cells and adjacent epithelial cells. Often, synaptic specializations could be recognized between NEE cells and nerve terminals. Electron-microscopical immunocytochemistry confirmed that the intraepithelial serotonin-containing cells correspond to the cells with NEE characteristics. Moreover, two types of NEE cells could be distinguished in newly hatched quail lungs. Both types showed serotonin immunoreactivity selectively distributed over the dense-cored vesicles, but somatostatin- and bombesin-like immunoreactivities were only noted in one of the NEE cell types and were never seen colocalized. Thus, the avian NEE system too, harbors at least three different bioactive substances and has a morphology comparable to that of mammals, reptiles and amphibians. © 1994 Wiley-Liss, Inc.
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  • 192
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    The @Anatomical Record 239 (1994), S. 75-87 
    ISSN: 0003-276X
    Keywords: Atrium ; Canine ; Dendrites ; Ganglionated plexus ; Nucleoli ; Pseudounipolar neurons ; Ventricle ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: A three-dimensional description of the distribution and organization of the canine intrinsic cardiac nervous system was developed in order to characterize its full extent physiologically.Methods: The anatomy of the canine intrinsic cardiac nervous system was investigated in 67 mongrel dogs by means of visulization following methylene blue staining as well as by light and electron microscopic analyses.Results: Collections of ganglia associated with nerves, i.e., ganglionated plexuses, were identified in specific locations in epicardial fat and cardiac tissue. Distinct epicardial ganglionated plexuses were consistently observed in four atrial and three ventricular regions, with occasional neurons being located throughout atrial and ventricular tissues. One ganglionated plexus extended from the ventral to dorsal surfaces of the right atrium. Another ganglionated plexus, with three components, was identified in fat on the left atrial ventral surface. A ganglionated plexus was located on the mid-dorsal surface of the two atria, extending ventrally in the interatrial septum. A fourth atrial ganglionated plexus was located at the origin of the inferior vena cava extending to the dorsal caudal surface of the two atria. On the cranial surface of the ventricles a ganglionated plexus that surrounded the aortic root was identified. This plexus extended to the right and left main coronary arteries and origins of the ventral descending and circumflex coronary arteries. Two other ventricular ganglionated plexuses were identified adjacent to the origins of the right and left marginal coronary arteries. Intrinsic cardiac ganglia ranged in size from ones comprising one or a few neurons along the course of a nerve to ones as large as 1 × 3 mm estimated to contain a few hundred neurons. Intrinsic cardiac neuronal somata varied in size and shape, up to 36% containing multiple nucleoli. Electron microscopic examination demonstrated typical autonomic neurons and satellite cells in intrinsic cardiac ganglia. Many of their axon profiles contained large numbers of clear, round, and dense-core vesicles. Asymmetrical axodendritic synapses were common.Conclusions: The canine intrinsic cardiac nervous system contains a variety of neurons interconnected via plexuses of nerves, the distribution of which is wider than previously assumed. © 1994 Wiley-Liss, Inc.
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  • 193
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 239 (1994), S. 88-94 
    ISSN: 0003-276X
    Keywords: Prothymosin alpha ; Proliferating cell nuclear antigen (PCNA) ; 5-Bromodeoxyuridine ; Proliferation markers ; Adrenal ; Glomerulosa ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Prothymosin alpha (ProT) is a polypeptide widely distributed in the organism and expressed by cell types with a high proliferative capacity. The aim of the current work was to investigate if ProT was localized in the progenitor compartment of the adrenal cortex which, following the cell migration theory, corresponds to the zona glomerulosa.Methods: We studied by immunohistochemical and in situ hybridization methods the distribution of ProT in rat and human adrenal cortex. Immunohistochemical techniques for the study of the proliferating cell nuclear antigen (PCNA) and incorporation of 5-bromo-2′-deoxyuridin during DNA synthesis were also done. Immunoelectron microscopic procedures were performed to determine the exact subcellular localization of ProT.Results: ProT was found in the zona glomerulosa cells, but not in the cells of the remaining cortical layers (zonae fasciculata and reticularis). Glomerulosa cells showed immunostaining for ProT only in the nuclei, excluding the nucleoli. Variability in immunostaining intensity was found between different glomerulosa cells. In situ hybridization of ProT mRNA confirmed that ProT synthesis in adrenal cortex occurs only in the zona glomerulosa. The results obtained for proliferating cell nuclear antigen and incorporation of 5-bromo-2′-deoxyuridin confirmed that adrenocortical proliferation occurs in the zona glomerculosa. Ultrastructural immunocytochemistry showed labelling for ProT over the euchromatin, but not on the heterochromatin aggregations nor the nucleoli.Conclusions: The results presented here: (1) support the migration theory for the adrenocortical cell renewal, (2) demonstrate that ProT is present in the nuclei of proliferating cells (being associated with euchromatin), and (3) suggest that the study of ProT expression would be useful in distinguishing cycling from resting cells. © 1994 Wiley-Liss, Inc.
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  • 194
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 239 (1994), S. 95-102 
    ISSN: 0003-276X
    Keywords: Steroidogenesis ; Actin ; Adrenal cortex ; Immunoelectron microscopy ; Rat ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Differences in the cytoskeletal protein actin in cells from the zona glomerulosa and zona fasciculata would be of considerable interest because there is persuasive evidence that rat corticosteroids are secreted by mechanisms that are somewhat zone-specific. We have previously shown evidence that actin may be involved in steroid secretion, possibly in connection with changes in adrenocortical microvilli. However, the cells upon which the data were based were not separated according to zone of origin.Methods: Immunogold electron microscopy and morphometric procedures were used to determine whether ACTH-induced changes in the peripheral cytoplasm of isolated adrenocortical cells occur in both zona fasciculata and zona glomerulosa cells.Results: Actin immunoreactivity was more concentrated in the cytoplasm adjacent to the plasma membrane (including the cytoplasm within the microvilli) than it was in the internal cytoplasm in cells from both zones (4-6 times more concentrated in zona glomerulosa cells and 3-6 times more concentrated in zona fasciculata cells). However, the mean aggregate microvillar surface length (microvillar index) of untreated zona fasciculata cells previously reported (Loesser and Malamed, 1987) was 23% greater than that of untreated zona glomerulosa cells. Although ACTH (at a maximal steroidogenic concentration) had no effect on the peripheral cytoplasmic actin concentration of zona glomerulosa cells, there was a 24% increase in the aggregate microvillar length. In contrast, in zona fasciculata cells, ACTH treatment was accompanied by an increase in peripheral cytoplasmic actin concentration of 58-64% and an increase in aggregate microvillar surface length of 40% (previously reported (Loesser and Malamed, 1987)), almost twice that for zona glomerulosa cells.Conclusion: The results suggest that ACTH-induced hormone release from zona fasciculata cells is mediated by increases in peripheral cytoplasmic actin and aggregate microvillar length; in zona glomerulosa cells such changes are small or absent. © 1994 Wiley-Liss, Inc.
    Additional Material: 7 Ill.
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  • 195
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 239 (1994) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 196
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 239 (1994), S. 103-112 
    ISSN: 0003-276X
    Keywords: Cell Rearrangement ; Convergent-Extension ; Gastrulation ; Growth ; Hensen's Node ; Mesoderm ; Mitosis ; Mitotic Spindles ; Neurulation ; Primitive Streak ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Formation and extension of the notochord (i.e., notogenesis) is one of the earliest and most obvious events of axis development in vertebrate embryos. In birds and mammals, prospective notochord cells arise from Hensen's node and come to lie beneath the midline of the neural plate. Throughout the period of neurulation, the notochord retains its close spatial relationship with the developing neural tube and undergoes rapid extension in concert with the overlying neuroepithelium.Methods: In the present study, we examined notochord development quantitatively in mouse embryos. C57BL/6 mouse embryos were collected at 8, 8.5, 9, 9.5, and 10 days of gestation. They were then embedded in paraffin and sectioned transversely. Serial sections from 21 embryos were stained with Schiff's reagent according to the Feulgen-Rossenbeck procedure and used for quantitative analyses of notochord extension.Results: Quantitative analyses revealed that extension of the notochord involves cell division within the notochord proper and cell rearrangement within the notochordal plate (the immediate precursor of the notochord). In addition, extension of the notochord involves cell accretion, that is, the addition of cells to the notochord's caudal end, a process that involves considerable cell rearrangement at the notochordal plate-node interface.Conclusions: Extension of the mouse notochord occurs similarly to that described previously for birds (Sausedo and Schoenwolf, 1993 Anat. Rec. 237:58-70). That is, in both birds (i.e., quail and chick) and mouse embryos, notochord extension involves cell division, cell rearrangement, and cell accretion. Thus higher vertebrates utilize similar morphogenetic movements to effect notogenesis. © 1994 Wiley-Liss, Inc.
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  • 197
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 239 (1994), S. 119-125 
    ISSN: 0003-276X
    Keywords: Immunocytochemistry ; M-cadherin ; Muscle regeneration ; Myoblasts ; Myotubes ; Satellite cells ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Cadherins are transmembrane proteins mediating calcium-dependent cell-cell adhesion in a cell type-specific manner by means of homophilic binding. M(muscle)-cadherin is a recently detected member of the cadherin family.Methods: We have investigated the localization of M-cadherin innormal and aneurally regenerating skeletal muscle of rat by means of pre-embedding immunocytochemistry. The antibody was directed against the extra-cellular domain of M-cadherin.Results: Myoblasts and myotubes in regenerating muscles tended to be arranged in clusters enclosed by a common basal lamina. Satellite cells of mature muscle fibers were attached to the underlying fiber without separating basal lamina. Reactivity for M-cadherin was restricted to the plasma membranes of myoblasts and satellite cells, and was most intense at the membrane areas facing adjacent myotubes or myofibers. Myoblasts interposed between two myotubes were stained on the entire surface. The adjacent plasma membrane of the otherwise negative myotube or muscle fiber, was stained as well, and extracellular reaction product was in the gap between the cells.Conclusion: The cellular localization of M-cadherin may indicate that M-cadherin is involved in calcium-dependent adhesion between satellite cells and muscle fibers or, by means of interposed myoblasts, between the clustered myotubes in a regenerating muscle. © 1994 Wiley-Liss, Inc.
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  • 198
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 239 (1994), S. 126-136 
    ISSN: 0003-276X
    Keywords: Argentophilic proteins ; Extraction ; Western blot ; Spermiogenesis ; Spermatozoa ; Rat ; Bovine ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Silver-stainability (argentophilia) of cytoplastmic structures occurring in spermatids have been localized into the organizing perinuclear theca, but the biochemical nature and structural associations of these proteins with the cytoskeletal and membranous elements are unresolved and, therefore, were the aim of the present study.Methods: Light and electron microscopic analysis of the silver-stainability in the rat spermatids and spermatozoa was carried out in the intact testis tissue and epididymal spermatozoa and after their chemical and mechanical extraction. Correlation of argentophilia with specific proteins of rat and bovine spermatids and spermatozoa was investigated using a recently developed technique for silver nitrate staining of proteins on nitro-cellulose.Results: Sequential formation of the silver-stainable domains seemed to proceed from the argentophilic acrosomal ring. Various extractions indicated that argentophilia in the spermatids and spermatozoa was mainly associated with the perinuclear theca and to some extent to the plasma membrane. Hyamine-soluble extract from spermatozoa of rat and bull revealed only a single argentophilic protein of 130 kDa. Hyamine and SDS-soluble extracts of rat testis tissue contained an additional group of argentophilic polypeptides of lower molecular weight (115, 94, 36, 23, and 21 kDa).Conclusions: Reduction in the number of argentophilic proteins appears to be involved in a series of changes in the cyto-architecture of developing spermatids. Tentative cytoskeletal nature of argentophilic proteins remains to be identified. Nevertheless, they may have important physical relations with the higher-order organization of the sperm head cytoskeleton and overlying membranes. © 1994 Wiley-Liss, Inc.
    Additional Material: 17 Ill.
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  • 199
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 239 (1994), S. 453-467 
    ISSN: 0003-276X
    Keywords: Electron microscopy ; Glycoconjugates ; Lectins ; Light microscopy ; Serous and mucous cells ; Submucosal laryngeal glands ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: The respiratory submucosal glands are a major source of secretions in the airway. Human submucosal laryngeal glands have been scarcely studied, with no works existing about their ultrastructure and histochemistry.Methods: Samples of epiglottis, ventricle, false vocal folds and true vocal folds were fixed in 10% buffered formalin for histochemical study with conventional and carbohydrate lectin histochemistry. Other samples were fixed in 2.5% glutaraldehyde and conventionally processed for transmission electron microscopy.Results: The human submucosal laryngeal glands are composed of serous tubules; mucous tubules; collector duct; and final portion of this duct. The serous cells showed sialosulphomucins and affinity for WGA and Con-A lectins. With a previous treatment with neuraminidase, they also labelled with PNA. The mucous cells contained sialosulphomucins and showed affinity for WGA and DBA lectins in the samples proceeding from blood group A, and for WGA, UEA-I and LTA with those from blood group O. Ultrastructurally, the serous cells presented a wide variety of granules, cells in which seromucous granules predominated. The mucous cells presented larger-sized granules which were very electron-lucent. The collector duct was composed of mitochondria-rich cells and basal cells. A cell which we have termed “intermediate” was identified in the transition zone between the mucous tubules and the collector duct, and in the final portion of the collector duct. It had morphological characteristics as if it were a transition between a goblet cell and collector duct cell. Some nerve endings with cholinergic and peptidergic vesicles were found among the myoepithelial cells.Conclusions: These glands presented some histological differences from the bronchial glands, the mucous secretion was related to the blood group antigens, and the serous cells showed a wide variability in their secretory granules, many of them being of a seromucous type. © 1994 Wiley-Liss, Inc.
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  • 200
    ISSN: 0003-276X
    Keywords: Spinal malformations ; Lordosis ; Perinotochordal connective sheet ; Sparus aurata ; Larvae ; Histochemistry ; Immunohistochemistry ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: Spinal malformations in adult teleosts occur under natural conditions and, more frequently, in culture exploitations. Skeletal deformities are linked with dysfunctions in collagen metabolism. We studied axial deviations appearing in early larval stages of cultured sea bream (Sparus aurata, L.).Methods: To evaluate connective tissue components of normal and lordotic fish we used histochemistry (alcian blue, picrosirius-polarization, clorhydric orcein, fuchsin resorcin), immunohistochemistry (anti-collagen I, II, III, and IV), and specific enzymatic digestions. The results were evaluated by semiquantitative methods.Results: Lordosis appeared before a vertebral column was developed, thus affecting the only skeletal structure present in the animal body, the notochord. At this stage the animal depends on the vitelline sac and an inflated swim-bladder is missing. The region of the curvature showed strong alterations in the arrangement of the muscle bundles and irregularities in notochord and perinotochordal collagen sheet. Histochemical and immunocytochemical analysis of the periotochordal sheet revealed the presence of type II collagen, non-sulfated glycosaminoglycans, and elastic fibers in normal and lordotic specimens. Low collagen-proteoglycan interactions occurred in lordotic animals.Conclusions: Lordosis in Sparus aurata originated during embryonic development and was characterized by disorganized connective tissue and muscle bundles. No major differences in connective tissue constituents were seen with respect to normal specimens. © 1994 Wiley-Liss, Inc.
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