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  • 1980-1984  (842)
  • 1981  (842)
  • Life and Medical Sciences  (842)
  • Nuclear reactions
  • 1
    ISSN: 0886-1544
    Keywords: videomicroscopy ; differential interference microscopy ; streaming ; reticulopodial motility ; Allogromia ; microtubules ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: A new method called Allen Video-enhanced Contrast, Differential Interference Contrast (AVEC-DIC) microscopy is shown to be sufficiently sensitive to detect several new features of microtubule-related motility in the reticulopodial network of the foraminifer, Allogromia. The method takes advantage of the variable gain and offset features of a binary video camera to operate the DIC microscope under conditions highly favorable for video imaging, but in which the optical image is virtually invisible to the eye yet retains its full information when viewed by a suitable video camera. The improvements are made possible by setting a dé Senarmont compensator to λ/9-λ/4 at maximal working aperture of internally corrected planapochromatic objectives. Under these conditions, the offset feature of the video camera can reject so much stray light from the instrument and specimen that contrast compares favorably with that observed in high-extinction images, and polarizing rectifiers offer scarcely any advantage. Freed from the constraints of the light-limited conditions of DIC microscopy, video images can be recorded 60 times per second, or over 1,000 times the rate of photomicrographs at comparable magnifications under high-extinction conditions.Application of this method to the reticulopodial network of Allogromia has shown that cytoplasmic organelles are translocated only in contact with single microtubules or bundles of microtubules, and that these organelles fail to move when separated from microtubules. Microtubules themselves undergo both axial translatory (“sliding”) and lateral “zipping and unzipping” movements that have been suggested to occur during mitosis and other biological processes.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 329-347 
    ISSN: 0886-1544
    Keywords: actin ; microfilaments ; heavy meromyosin ; mammary gland ; secretion ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Cytochalasin B, a microfilament-altering drug, inhibits lactose synthesis in lactating guinea pig mammary gland [Biochim. Biophys. Acta 392:20, 1975] but not primarily by inhibiting glucose transport [Eur. J. Cell Biol. 20:150, 1979]. In order to study the possible role of microfilaments in lactose synthesis and secretion, we isolated both the alveolar (milk-secreting) and myoepithelial (contractile) cells from lactating mammary gland. Light microscopy shows that the alveolar cell fraction (viability approximately 71%) is homogenous and that the cells retain strong polarity of secretory structures in the apical region. Two proteins were extracted from the alveolar cell fraction. One (mol wt 42,000) comigrates with skeletal muscle actin on SDS-PAGE gels. The other, a high-molecular-weight (180,000) protein (HMWP) may be analogous to actin-binding protein or clathrin. An extract from the myoepithelial cell fraction also contains a protein that comigrates with actin but no HMWP. Whole tissue extract contains the 42K protein, and a 185K HMWP. Examination of the alveolar cell extract by electron microscopic (EM) negative staining revealed meshworks of multistranded, interconnecting filaments, with attached globular structures (100-200 A) (possibly the HMWP) and single filaments (40-60 A diameter) branching off. To localize these filamentous structures in situ, whole tissue was glycerinated and incubated with rabbit skeletal muscle heavy meromyosin (HMM). Masses of filaments in myoepithelial cells served as convenient standards for HMM decoration. Decorated filaments have cross-arms or projections, unlike the narrow, smooth filaments of control tissue. Decorated filaments in alveolar cells are located beneath the plasma membrane, in close association with secretory vacuoles, and near the Golgi apparatus; filaments near the latter two are often oriented perpendicular to the plasma membrane. Microvesicles are embedded in meshworks under the plasmalemma and near the Golgi apparatus. Intermediate-sized (85-115 A diameter), non-decorated filaments diverge from the meshworks of decorated filaments. Microvesicles are associated with intermediate-sized filaments as well. The association of actin-like filaments with secretory vacuoles and microvesicles and their location in areas of the cell concerned with biosynthetic activities suggest a possible function in the intracellular transport of secretory products.
    Additional Material: 13 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 455-468 
    ISSN: 0886-1544
    Keywords: intercellular bridge ; intercellular communication ; cytokinesis ; squid ; ultrastructure ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Incomplete cytokinesis followed by the disappearance of the midbody and spindle remnant results in intercellular bridges between the cells of the blastoderm of the squid embryo. An electron microscope study of the morphology of the stages of development of the intercellular bridge is presented. Cytokinesis ceased as the furrow base reached a diameter slightly larger than the midbody. As furrowing stopped, a dense material accumulated to form a cylindrical sheath 50 nm thick, lining the inner surface of the furrow base. Proteolytic enzymes showed this material to have a significant protein component. As the midbody broke down, vesicles lined the inner surface of the bridge sheath. In this configuration, there was cyto-plasmic continuity between the cells, and organelles appeared to pass through the bridge.The intercellular bridge could become temporarily closed. Vesicles entered the channel and fused with the vesicles lining the inner surface of the sheath. The vesicles enlarged until the channel became occluded with a series of transverse cisternae, the edges of which were embedded in the material of the sheath. When the bridge reopened, the transverse cisterna appeared to dissociate from the sheath, move out of the channel, and break down. Occasionally bridges were seen in which the bridge wall appeared distorted into lobes. It is suggested that such bridges might be in the porcess of breaking down, resulting in the final separation of the cells.
    Additional Material: 16 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 469-483 
    ISSN: 0886-1544
    Keywords: microtubules ; nucleation ; mitosis ; nocodazole ; immunocytochemistry ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The reassembly of microtubules is described in mitotic cells after release from nocodazole-induced block. The formation of microtubules was followed by light microscopic immunocytochemical staining using the PAP method, combined with to-luidine blue staining of the chromatin. The light microscopic observations on whole cells were compared with ultrastructural observations on thin sections. This step is essential to ascertain complete destruction of microtubules during the nocodazole treatment and to correlate immunocytochemical staining with the presence of microtubules.Removal of nocodazole (10 or 1 μg/ml) after a sufficiently long incubation to induce a complete disappearance of microtubules resulted in the appearance of tubulin staining specifically associated with the centromeres and with one or two isolated points in the cytoplasm. Electron microscopy confirmed that the staining was due to the massive accumulation of small microtubules at the kinetochores and centrosomes. Kinetochore nucleation was seen only in association with condensed metaphase-stage chromosomes and not with the less-condensed prophase chromosomes.In a second type of experiment cells were allowed to enter mitosis in the presence of an incompletely active concentration of nocodazole (0.1 μg/ml). The construction of the mitotic spindle was arrested; however, short microtubules were assembled at the kinetochores and centrosomes.These experiments demonstrate that in living mitotic PTK2 cells the kinetochores, as well as the centrosomes, exert a nucleating action on tubulin assembly.The further elongation of microtubules after removal of nocodazole was seen to occur preferentially along axes between the centrosomes and the kinetochores. This resulted in the construction of normal metaphases that evolved through anaphase and telophase. We have attempted to formulate a hypothesis that may explain the oriented assembly that seems to be essential in the construction of the spindle.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 485-497 
    ISSN: 0886-1544
    Keywords: actin ; tubulin ; nucleotides ; polymerization ; microfilaments ; microtubules ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Both actin and tubulin, the major proteins of the cytoskeleton, bind nucleotide triphosphate (NTP) and exhibit the phenomenon of “polymerization-coupled” NTP hydrolysis. In this report I review the nature of polymerization-coupled NTP hydrolysis, and its possible role in the cellular function of actin and tubulin. Polymerization-coupled hydrolysis may be viewed as simply reflecting differences in the NTPase activity of free subunit as compared to polymer. Making assumptions concerning the values of various rate constants, it is possible to write expressions for the effects of NTP hydrolysis on the kinetics of polymerization. The role of NTP hydrolysis may be viewed in at least three different ways: (1) Hydrolysis alters the kinetics of assembly and disassembly. This leads to a consideration of the role of subunit flow in microtubule and microfilament function. (2) Hydrolysis is an essentially irreversible step that separates the assembly and disassembly reactions. This suggests a role of NTP in the regulation of polymer content during cellular cycles of assembly and disassembly. (3) NTP may allow transient stabilization of intersubunit bonds. This suggests a role of NTP in nucleation and possible regulation of nonequilibrium states of assembly.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 499-515 
    ISSN: 0886-1544
    Keywords: dynein ; tubulin ; axonemes ; microtubules ; microtubule-associated proteins ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Microtubule-associated proteins (MAPs), isolated from brain tubulin, bound to and saturated outer fibers of Chlamydomonas flagella. MAPs present on these microtubules prevented the subsequent recombination of dynein. MAPs also bound to intact axonemes and thus did not specifically bind to the dynein binding sites on the A subfiber. A molar ratio of 1 mole MAP2 per 27 moles tubulin dimers at saturation of the outer fibers with MAP2 suggested that MAPs could effectively interfere with dynein recombination only if the MAPs were near the dynein binding sites to sterically prevent binding. However, electron microscopic observations indicated that MAPs were not localized but, instead, were dispersed around the outer fibers. In addition, MAP2 present at saturating amounts on in vitro assembled brain microtubules had no significant effect on dynein binding. Dynein-decorated microtubules contained clusters of arms suggesting that there may be cooperative interaction between the arms during dynein binding. Because the A subfiber of axonemes contains sites to which dynein preferentially attaches, MAPs may prevent recombination by interfering with cooperative binding to these specific sites. Dynein presumably binds with equal affinity to any protofilament on in vitro assembled microtubules, and, therefore, the MAPs may not be capable of effectively interfering with cooperative binding of dynein to these microtubules.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 167-178 
    ISSN: 0886-1544
    Keywords: nerve growth ; actin ; tubulin ; antibodies ; immunofluorescence ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Embryonic chick nerve cells, from dissociated dorsal root ganglia, were cultured on polylysine substrata and examined for tubulin and actin distribution by indirect immunofluorescence.Antibodies generated against chick brain tubulin produced specific fluorescence in growth cones, neurites, and cell bodies without revealing distribution differences or substructure in the nerve cells. However, at reduced antitubulin concentrations, differences were resolved. Tubulin fluorescence remained uniform and intense in neurites and cell bodies, but exhibited reduced intensity and patterning in growth cones. Nonneuronal cells in the reduced intensity and patterning in growth cones. Nonneuronal cells in the cultures served as controls for typical cytoplasmic tubulin fluorescence distribution. Straining controls demonstrated that fluorescence resulted from tubulin-antitubulin binding.Analogous studies, using antibodies generated against chick brain actin, demonstrated distribution differences at reduced antiactin concentrations, including “hot spots” of intense fluorescence in growth cones and a paucity of fluorescence in neurites.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 237-245 
    ISSN: 0886-1544
    Keywords: centrioles ; symmetry ; triplet blades ; thermal fluctuations ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The paper suggests several principles of construction of a microscopically small device for locating the directions of signal sources in microscopic dimensions. It appears that the simplest and smallest device that is compatible with the scrambling influence of thermal fluctuations as are demonstrated by Brownian motion is a pair of cylinders oriented at right angles to each other. Nine equally spaced blades run in a pitched fashion along the mantle of each cylinder. The blades have a concave cross-section and bend around the circumference of the cylinder in a certain rotational pattern. Considering the striking similarity of this hypothetical device with centrioles, the paper puts forward the conjecture that centrioles locate the direction of hypothetical signals inside cells.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 247-260 
    ISSN: 0886-1544
    Keywords: cilia ; trachea ; ATP-reactivation ; ciliary activity ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Evidence for active sliding of microtubules during ciliary activity has been demonstrated in a number of organisms: sea urchin sperm flagella, protozoan cilia, and mollusc gill cilia. Although there is evidence that active sliding also occurs in mammalian sperm flagella, there is little or no information on whether active sliding of microtubules also occurs in the short (5-μm) cilia of the mammalian trachea or oviduct. Since these cilia are important in tracheobronchial clearance and ovum transport, respectively, it has been important to demonstrate that microtubule sliding is also involved in the activity of somatic cilia. Ciliated apical portions (cortices) and cilia were isolated from rabbit trachea and oviduct, using Triton X-100 to demembranate the cilia. Most of the ciliated cortices reactivated upon addition of ATP, whereas isolated cilia reactivated to a lesser extent. When preparations of cilia were digested with trypsin before or after ATP addition, disintegration of axonemal doublets occurred with about the same frequency as reactivation. These events were recorded using Nomarski optics and dark-field microscopy. When isolated cilia which had been digested by trypsin and exposed to ATP were also prepared for electron microscopy by negative staining, telescoping of doublet microtubules from axonemes could be shown. These results demonstrate that mammalian somatic ciliary doublet microtubules actively slide in a manner similar to that described for invertebrate cilia.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 269-272 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 261-268 
    ISSN: 0886-1544
    Keywords: Tetrahymena ; chemotaxis ; temporal-gradient sensing ; modulation of turning frequency ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The motility pattern of Tetrahymena thermophila in a homogeneous attractant field consists of successive “runs” and “turns.” The turning frequency decreases or increases upon an abrupt increase in attractant or repellent concentration, respectively. The dose-response curve for leucine and methionine yields a saturation curve with half maximum modulation of the turning frequency at a concentration of 15 μM and 2 μM, respectively. The turning frequency is modulated at a threshold concentration of 0.02 μM and 0.50 μM for leucine and methionine, respectively. The decrease (increase) in turning frequency in the presence of an attractant (repellent) jump reverts to prestimulus frequency in a time proportional to the concentration jump. Hence, Tetrahymena seem to employ temporal-gradient sensing for chemotaxis. Spatial-gradient taxis is thus exerted by random walk, which is biased in the direction of the gradient.
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 273-273 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981) 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 14
    ISSN: 0886-1544
    Keywords: videomicroscopy ; polarization microscopy ; streaming ; reticulopodial motility ; Allogromia ; microtubules ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: A new method is described for recording rapid processes of cell motility in polarized light. The Allen video-enhanced contrast (AVEC-POL) method of polarization microscopy achieves significant improvements in resolution, contrast, and the visibility of fine detail by a combination of novel adjustments to a standard (unrectified) polarizing microscope and video camera. Using the full working aperture of a high-power planapochromatic objective lens and compensator setting of λ/9-λ/4, visible images appear lacking in contrast. However, the same images viewed with an appropriate video camera equipped with an electronic offset adjustment can be made to appear with as much contrast as desired, revealing a significantly greater amount of fine detail in the image than can be seen by high extinction visual microscopy alone. At bias retardations between one-ninth and one-quarter wave, the diffraction anomaly observed near extinction disappears. Consequently, polarizing rectifiers are not required with the AVEC-POL method, and images previously requiring photographic exposures of around 20 seconds are sufficiently bright to be registered on the video monitor in 1/60 second. Using an intensity monitor, quantitative measurements of cellular birefringence can be retrieved from live or videotaped images displaying a linear relationship between contrast and phase retardation due to birefringence. The AVEC-POL method also renders accessible to polarized light analysis a number of objects that scatter or depolarize too much light to be studied by high extinction methods. The method is demonstrated on model objects and applied to the highly motile reticulopodial network of Allogromia laticollaris. Rapid motion in close association with microtubules can now be analyzed in greater detail at a significant reduction in the cost of recording.
    Additional Material: 10 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 303-327 
    ISSN: 0886-1544
    Keywords: cilia ; microtubules ; ATPase ; vanadate ; geometry of sliding ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: A dynein arm attachment cycle produces sliding between adjacent doublet microtubules (N and N + 1) of cilia. In intact axonemes, in the absence of ATP, almost all arms appear attached at both ends (rigor). When ATP is added, most arms detach from doublet N + 1. In ATP and vanadate, the arms do not return to rigor, suggesting that ATP hydrolysis is required for re-extension and reattachment of the dynein arm, but not for detachment. Using solutions containing dynein to decorate dynein-less axonemal doublets, we confirm this interpretation. In the absence of ATP, both sides of each doublet decorate with arms. Addition of ATP, ATP and vanadate or AMP-PNP causes immediate arm detachment, but only in the first instance, where extensive ATP hydrolysis can occur, does decoration eventually reappear. Dynein decorates heterologous axonemal doublets and brain microtubules, as well as homologous doublets, suggesting that this mechanochemical cycle may have general applicability in microtubule-based cell motility.
    Additional Material: 111 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 433-443 
    ISSN: 0886-1544
    Keywords: Physarum ; acellular slime mold ; calcium ion ; calcium-ionophore ; cytoplasmic contraction ; oscillation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Calcium is now generally thought to play a key role in regulating a variety of cellular movements. When the plasmodium of Physarum polycephalum was treated with the calcium-ionophore A23187 or the quasi-ionophore amphotericin B, Ca2+ leaked out. Ca2+ efflux into the ambient solution from the plasmodial strand segment was measured by the luminescence of a photoprotein aequorin, and the tensile force production was recorded simultaneously. Ca2+ efflux oscillated with the same period as the cycle of tension generation in the strand, but the phase of cyclic changes in Ca2+ efflux was opposite to that of tension generation. That is, Ca2+ efflux fell in the increasing tension phase and rose in the decreasing tension phase. Cyclic changes in efflux of Ca2+ are provisionally interpreted as reflecting corresponding changes in concentrations of free Ca2+ in the cytoplasm.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 445-454 
    ISSN: 0886-1544
    Keywords: taxol ; microtubules ; polymerization ; tubulin ; mitotic inhibitor ; protein self-assembly ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Dissociated bovine brain microtubule protein has been shown to reassemble at 0°C in the presence of the drug taxol. Tubulin polymerization was monitored both by electron microscopy of the polymeric structures and by incorporation of tritiated GTP into filterable polymeric structures. Most of the labeled guanine nucleotide uptake into tubulin polymeric structures occurred in the first 30 minutes of incubation with the drug. The initial polymerization event results in the formation of protofilamentous tubulin ribbons. The first microtubules were noted after 1 hour of incubation with the drug. After 20 hours of incubation at 0°C with taxol, the bulk of the polymerized tubulin appeared to be in the form of microtubules. Cold-stable tubulin rings with a mean diameter of 34 nm were present in the reaction mixture before the addition of taxol and throughout the 20-hour incubation. Most of the rings were apparantly not involved in the taxol-induced microtubule assembly. The results are consistant with a model whereby taxol induces an initial formation of protofilamentous ribbon structures, mostly from free tubulin dimers, and a slower subsequent folding of the ribbon structures into microtubules.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 179-192 
    ISSN: 0886-1544
    Keywords: actin ; echinoderm ; fascin ; filopodia ; actin cross-linking protein ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Echinoderm coelomocytes transform from petaloid cells with large motile lamellipodia to filopodial forms. During this morphological transformation, actin filaments extensively reorganize from a random meshwork into tight bundles, which become the skeletons or cores of the filopodia. Antibody localization procedures show that fascin, a 58,000 dalton actin cross-linking protein, becomes incorporated into the filament bundles as they form. Isolated filopodial cores have a pronounced transverse striping pattern, which has been previously identified with fascin crosslinks, and gel electrophoresis identifies a protein in the cores that co-migrates with purified egg fascin. A few of the core fragments also have a distinctive “cap,” which we presume is the membrane insertion site for actin filaments.We have developed a radioimmunoassay for fascin and have used it to study the redistribution of this protein during transformation. Data from the assay indicate that fascin constitutes about 5% of the total cell protein and that substantially more fascin, approximately 1.5-2 times more, is found in the Triton-insoluble cytoskeletons of the filopodial cells than in the petaloid cells. Actin, measured by the DNAase I inhibition assay accounts for approximately 10% of the total cell protein. Approximately 65% of this actin is in a soluble non-filamentous form in the petaloid cells. Our results show that actin polymerization must occur during the cell shape change, since we find approximately 25% more actin in the filopodial cytoskeleton than in the petaloid cytoskeleton. The results show a preferential incorporation of fascin into the cytoskeleton as the cells form filopodia.
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 193-203 
    ISSN: 0886-1544
    Keywords: polygonal network ; rat aortic smooth muscle cell ; cell culture ; electron microscopy ; amino acid analysis ; elastin ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Cultured rat aortic smooth muscle cells (SMC) were examined by electron microscopy and found to contain polygonal networks of 75 A° thin myofilament bundles. The cells also had large bundles of longitudinally aligned thin myofilaments with periodically spaced dense bodies. Abundant plasmalemmal vesicles were present at the cell periphery, and the cells were connected by desmosomes. Intercellular spaces contained sparse amounts of elastic fibers, a material generally present in SMC cultures. Analyses of amino acids by automated column-chromatography showed that isodesmosine and desmosine, two amino acid residues unique for elastin, were present. Accordingly, it was concluded that polygonal networks, previously detected solely in cultured nonmuscle cells, were present in SMC.Other findings suggest (1) a change in myofilament arrangement takes place during cell migration, and (2) rat aortic SMC grown in tissue culture flasks is an important experimental tool in the study of cell motility since such myofilament rearrangements were observed to occur up to fourteen days in first passage.
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 205-235 
    ISSN: 0886-1544
    Keywords: capping of receptors ; cell locomotion ; cell-surface interactions ; frictional force ; membrane flow ; polymorphonuclear leukocytes ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: As a cell moves over a surface, the distribution of membrane proteins that adhere to the surface will be changed relative to the distribution of these molecules on a static cell. Observations of this redistribution offer, in principle, evidence as to the mechanisms of membrane dynamics during cell locomotion. Toward extracting such information we present and analyze a mathematical model of receptor transport in the membrane by diffusion and convection, as affected by the making and breaking of the bonds between the receptors and the surface as the cell moves.We show that the disruption of receptor-surface bonds at the tail of the cell provides a mechanism by which the frictional force opposing a cell's motion is exerted, and calculate the magnitude of this force as a function of cell velocity. Assuming this to be the major contribution to the frictional force, we show that when the shear force on a cell is above a critical value it is no longer possible for the cell to slide across the surface. For such large forces, it is still possible for the cell to roll; alternatively the cell can be torn free of the surface.Our analysis of existing data on movement of polymorphonuclear leukocytes indicates that cell motion is not accompanied by a bulk flow of membrane from the front to the back of the cell. The data also indicate that cells do not tend to roll as they move over a surface under normal conditions. The data are most consistent with a model where the membrane as a whole is stationary but where receptors that bind to the surface become coupled to sub-membrane contractile proteins.
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  • 21
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 1 (1981), S. 387-397 
    ISSN: 0886-1544
    Keywords: birefringence ; polarizing microscope ; sea urchin egg ; cortex ; mitosis ; cleavage ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Birefringence (BR) at the cell surface of fertilized eggs of the sand-dollar, Clypeaster japonicus, during mitosis and cleavage was determined with a photoelectric BR detection apparatus [Hiramoto et al, 1981a]. The cortex of about 2 μm thickness is birefringent positive with respect to the normal to the cell surface. The hyaline layer is negatively birefringent. The halo-layer consisting of a row of microvilli surrounding the egg is positively birefringent in normal Ca-free sea water, while it is negatively birefringent in Ca-free sea water with high refractive index. The BR of the cortex gradually increases over the entire surface during mitosis until the onset of cleavage. The BR of the cortex at the polar region reaches a maximum shortly after the onset of cleavage and then decreases, while the BR of the cortex at the equatorial region begins to decrease shortly before the onset of cleavage, reaches a minimum shortly after the cleavage starts, and then increases again as the cleavage furrow advances. The coefficient of birefringence of the cortex is about 2.5 × 10-5 at the maximum. The BR change of the cortex during mitosis and cleavage is interpreted as a passive deformation caused by the constriction of the contractile ring as well as an active structural change of the cortex occurring in the dividing cell.
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  • 22
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    Cell Motility and the Cytoskeleton 1 (1981) 
    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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  • 23
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    Cell Motility and the Cytoskeleton 1 (1981), S. 417-431 
    ISSN: 0886-1544
    Keywords: spindle poles ; centrioles ; cell center ; scaffold ; electron microscopy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: I have used fluorescence microscopy and antibodies to 10nm filaments and tubulin labelled with contrasting fluorochromes to compare the distribution of these proteins in endothelial cells during cell division. During interphase the two filament systems have entirely different distributions: The bulk of the 10nm filaments form a ring that surrounds the cell center and nucleus and remains parallel to the substrate, while the microtubules radiate from the cell center to the cell's border. When the mitotic spindle replaces the radial microtubule pattern in mitosis, the spindle poles remain within - and in close proximity to - the ring of 10nm filaments. This was confirmed by electron microscopy which showed the ring and centrioles in the same plane separated by a distance of 300-400 nm.
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  • 24
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    Cell Motility and the Cytoskeleton 1 (1981), S. 399-416 
    ISSN: 0886-1544
    Keywords: myosin heavy chain ; avian muscular dystrophy ; adult and embryonic fast white fibers ; slow red fiber ; rod ; subfragment-1 ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Avian muscular dystrophy is characterized by the degeneration of fast white skeletal muscle fibers, with onset during development. Using a one-dimensional peptide mapping technique, we have detected two forms of the myosin heavy chain in the fast white fibers of adult domestic chickens, one form characteristic of birds homozygous for muscular dystrophy, the other of their normal controls. Four dystrophic strains carrying the same gene for muscular dystrophy were examined.No differences were detected in the embryonic heavy chain peptide maps of normal and dystrophic chickens, consistent with the developmental onset of the condition. Differences were also absent from the peptide maps of heavy chains from slow red fibers, which are unaffected in dystrophy. No dystrophy-specific peptide map differences were detected in the three light chains. Analysis of peptide maps of rod and the heavy chain component of subfragment-1 from normal and dystrophic heavy chains indicates the presence of amino acid sequence differences in the two proteins.
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  • 25
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    Cell Motility and the Cytoskeleton 1 (1981) 
    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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  • 26
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    Cell Motility and the Cytoskeleton 1 (1981), S. 349-362 
    ISSN: 0886-1544
    Keywords: Ca2+ ; flagella ; symmetry ; vanadate ; spermatozoa ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Increased Ca2+ concentration causes a reversible increase in asymmetry of the flagellar bending waves of “potentially symmetric” demembranated sea urchin spermatozoa. When these flagella are immobilized with 5 μM vanadate, increased Ca2+ concentration causes a reversible increase in the total bend angle between the tip and the base of the immobilized flagella. These effects of Ca2+, and the movement which can be activated by CaATP2-, can be inhibited by vanadate, but in both cases, high concentrations of vanadate, of the order of 100 μM, are required. These observations suggest that ATP, possibly in the form of CaATP2-, is required for the Ca2+-induced change in shape of the flagella, but other observations suggest that the magnitudes of asymmetry and total bend angle are more closely related to Ca2+ concentration than to CaATP2- concentration.
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  • 27
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    Cell Motility and the Cytoskeleton 1 (1981), S. 363-370 
    ISSN: 0886-1544
    Keywords: Ca2+ ; Mg2+ ; symmetry ; flagella ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Potentially asymmetric spermatozoa are obtained when spermatozoa are demembranated in the presence of a low Ca2+/Mg2+ ion concentration ratio. They swim with asymmetric bending waves even when reactivated at low Ca2+ concentrations, and become more asymmetric when Ca2+ is increased. Potentially symmetric spermatozoa, which swim with symmetric bending waves at low Ca2+ and become asymmetric as the Ca2+ is increased, can be obtained by exposing the flagella to a high Ca2+/Mg2+ ratio, either during or subsequent to demembranation. The rate of this conversion is an increasing function of temperature and Triton concentration. Potentially symmetric spermatozoa can be reconverted to potential asymmetry, if the exposure to high Ca2+/Mg2+ is brief, and is terminated by addition of EGTA and Mg2+ before diluting the spermatozoa. The conversion to potential symmetry may involve removal of a labile component from the axoneme.
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  • 28
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    Cell Motility and the Cytoskeleton 1 (1981), S. 371-385 
    ISSN: 0886-1544
    Keywords: rotating filaments ; cytoplasmic streaming ; Nitella ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Our knowledge about the actin-containing characean filaments on the basis of light and electron microscopical investigations is reviewed. Dynamic filamentous networks, known already from isolated droplets, were detected in Nitella rhizoidal cells using light microscopical techniques. Earlier light microscopic observations in cytoplasmic droplets are confirmed and complemented by new model experiments with rotating helices. The motile phenomena occurring at the filament bundles (ring formation, wave propagation, particle translocation, net dynamics, rolling motions, formation of side arms) can, in this way, be imitated in detail. Thus, the concept of cytoplasmic streaming as a translocation along bundles of rapidly rotating helical filaments is supported. In order to explain unidirectional cytoplasmic streaming, a periodic winding up and unwinding of fine filaments is postulated by which ions are periodically bound and displaced. The formation of side arms which is favored during unwinding results in a screw-mechanical different behavior of the filaments in the two directions of rotation and therefore causes permanent particle transport in one direction.
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  • 29
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    The @Anatomical Record 199 (1981), S. 89-97 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The electron microscopic localization of insulin, glucagon, somatostatin, and pancreatic polypeptide (PP) in the pancreas of the iguanid lizard, Anolis carolinensis was studied by the unlabeled antibody peroxidase-antiperoxidase immunocytochemical technique. Insulin, glucagon, and somatostatin were localized absolutely to those cells previously identified on the basis of the characteristics of their secretory granules as being β cells, α cell, and D cells, respectively. The secretory granule cores of the PP-containing cells appeared to be ellipsoidal with a semi-major axis of 450 nm and a semi-minor axis of 365 nm. This previously unidentified cell type is named the F cell, in keeping with the localization of PP to the original F cell of the canine pancreas. Without immunocytochemical staining, the qualitative ultrastructural characteristics of the F cell secretory granules were inadequate to permit certain identification of the F cell, especially with regard to the D cell.
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  • 30
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    The @Anatomical Record 199 (1981), S. 129-137 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The epithelium of rat palatal mucosa was examined from 2 to 30 days after birth and changes in epithelial thickness, cellularity, average cell volume, mitotic activity and the turnover time of the nucleated cell layer were determined from histological sections. The mean epithelial thickness, which was 35.3 ± 1.5 μm at 2 days, remained constant for the first 9 days and then progressively increased, reaching 91.7 ± 1.7 μm by 30 days. This change in thickness was partly bought about by a doubling of the number of nucleated cells per mm2 of the surface, from 90.4 ± 2.81 × 103 to 187.63 × 5.654 × 103, and partly due to a change in the ratio of cells in the progenitor and maturing cell compartments, as assessed by the change in volume of an “average” epithelial cell. Mitotic activity also remained constant for the first 9 days and then increased, reaching levels five times greater than initial levels by 30 days. It is suggested that these changes are brought about by frictional stimulation associated with the initial intake of solid food as well as systemic influences related to general growth mechanisms.
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  • 31
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    The @Anatomical Record 199 (1981), S. 109-127 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Protein synthesis and secretion in mouse uterine glands during the peri-implantation period were studied, by both light and electron microscopic autoradiography, after the in vivo administration of tritiated leucine (3H-leucine) and proline (3H-proline). Light microscopic autoradiography revealed that the time course of synthesis and secretion of labeled proteins was constant during days four, five, and six of pregnancy. Labeled material could be detected in the glandular lumen by 45 minutes after administration and in higher concentrations by 90 minutes after administration.Analysis of electron microscopic autoradiographs from days five and six of pregnancy showed that high levels of activity were initially present over the rough endoplasmic reticulum and Golgi complexes and subsequently declined at the longer time intervals (45 and 90 minutes), while activity over the glandular lumen increased with time. The pathway of intracellular transport to the glandular lumen appeared to be via small cytoplasmic vesicles on both days five and six of pregnancy. Additional pathways for transport of the labeled protein to the glandular lumen appeared to be present in the form of the large vesicles on day five and granules on day six of pregnancy.Throughout the peri-implantation period, mouse uterine glands were active secretory structures in which the mode of secretion was similar to other exocrine cells. Thus, the uterine glands of the mouse must be considered a source of uterine fluid proteins at the time of implantation that may contribute to quantitative changes in these proteins.
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  • 32
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    The @Anatomical Record 199 (1981), S. 139-152 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 33
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    The @Anatomical Record 199 (1981) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 34
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    The @Anatomical Record 199 (1981), S. 177-186 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Urinary bladders and urethrae were collected from six adult and two juvenile female dogs. Five urethral regions and the neck and body of the bladder were sampled. Volume fractions for connective tissue including elastic fibers, smooth and striated muscle, and epithelium were obtained by projecting section images onto an array of points and computing the number of points overlying a tissue constituent per total points overlying the tissue section.Smooth muscle occupied approximately half the volume of the bladder wall, one-third the volume of the vesical neck, and one-fourth the volume of the proximal urethra. Striated muscle was present in the distal half of the urethra, where the total muscle coat occupied about one-third of the urethral wall volume. Smooth muscle was practically absent in the terminal urethra, where the striated urethralis muscle encircles urethra and vagina in common. Epithelial area and lumen perimeter were not significantly different along the length of the urethra except that urethral epithelium was significantly thicker adjacent to the vesical neck. In terms of histological proportions, the vesical neck was intermediate between the body of the bladder and the proximal urethra.
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  • 35
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    The @Anatomical Record 199 (1981), S. 187-195 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Urinary bladders and pelvic urethrae were collected from six adult and two juvenile male dogs. Within two vesical and six urethral sampling regions, volume densities were estimated for smooth and striated muscle, connective tissue and elastic fibers, stratum cavernosum, luminal epithelium, and prostate. The neck had significantly less smooth muscle and more connective tissue than the body of the bladder. In the prostatic urethra, smooth muscle was associated principally with trabeculae surrounding prostate lobules. Smooth muscle was sparse superficially in the prostatic capsule and practically absent in relation to the mid-prostatic urethra. Thus there was no mechanism for active closure of the middle prostatic urethra, and elastic fiber density was correspondingly high in this region. The smooth muscle sphincter needed to maintain urinary continuence and prevent semen reflux was primarily the vesical neck. Caudal to the body of the prostate, striated muslce comprised more than 50% of the urethral wall. Juvenile and adult postprostatic urethrae were similar except for a decreased quantity of stratum cavernosum in the pups.
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  • 36
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    The @Anatomical Record 199 (1981), S. 403-421 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The rostral pars distalis of the anterior pituitary gland of the marine alewife, Alosa pseudoharengus, during its annual spawning run to fresh water was examined histologically. The rostral pars distalis is composed of many interconnecting follicles of various sizes. Contrary to earlier reports, the follicular epithelium contains not only prolactin (PRL) cells but corticotropic (ACTH) cells and thyrotropic (TSH) cells (in addition to two nonendocrine cell types). Basally all three endocrine cell types make direct contact with the basement membrane which separates the follicles from the neurohypophysial processes. Apically, however, only the prolactin cells, the largest of the three, protrude into the follicular lumen by means of the small ciliated apical protruberance. All other cellular elements are sealed from the follicular lumen by a layer of covering cells which have properties of transitional epithelial cells. In the follicular epithelium, the slender TSH cells are intercalated between the large conspicuous prolactin cells. The ACTH cells, the smallest of the three endocrine cells, lie in deep invaginations in the basal regions of the individual PRL cells in such a way that on cursory examination they can be mistaken for the nuclei of the latter. Only a small portion of the cellular surface of the ACTH cell escapes the enveloping prolactin cell to make contact with the basement membrane of the follicle. In teleosts, prolactin, ACTH, and TSH have all been implicated in the regulation of hydromineral metabolism and reproductive development. The intimate spatial relation between the three endocrine cells in the alewife rostral pars distalis thus raises the possibility of some functional interactions at the adenohypophysial level, perhaps as an adaptation of this anadromous teleost whose reproductive development and behavior is associated with large changes in ambient salinity. The functional significance of the follicular lumen is discussed together with possible sensory functions of the PRL cells.
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  • 37
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    The @Anatomical Record 199 (1981), S. 433-439 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The purpose of this study was to determine (1) growth of the turtle shell and change in weight under constant controlled laboratory conditions and (2) whether under these constant conditions there were seasonal changes. Fifty unfed refrigerated eight-week-old hatchling turtles Chrysemys scripta were received in October and maintained in aquaria with 16 hours of artificial light and eight hours of darkness, at 24-27°C and a humidity of 30% and fed twice weekly. Gross linear measurements of the width and length of the plastron and carapace, and total body weights, were taken at eight weeks and thereafter at about six-week intervals. During the two-year period the mean increase of the plastron length was from 30.79 ± 0.19 mm to 68.32 ± 1.58 mm, plastron width from 24.23 ± 0.20 mm to 50.43 ± 1.03 mm; carapace length from 32.47 ± 0.24 mm to 75.21 ± 1.82 mm, carapace width from 31.81 ± 0.28 mm to 67.12 ± 1.29 mm, and body weight from 6.94 ± 0.15 gm to 80.63 ± 5.02 gm. Calculated daily percent changes revealed that as the turtles aged, the rates decreased. At 56 days of age, weight was the most strongly correlated with its value at 786 days of age. No seasonal differences in growth were noted between the summer and winter periods when turtles would enter winter dormancy in certain natural environments. Environmental factors are reflected in the growth of the turtle.
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  • 38
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    The @Anatomical Record 199 (1981), S. 441-448 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A live-born, one-day-old diprosopic piglet was presented to the Ontario Veterinary College. The piglet had a normal body with two heads, joined in the occipital region. There were two complete snouts, four eyes and three ears. The lower jaws were immobile because of overlapping mandibular rami. Although there was only one vertebral column, the bodies of the vertebrae, but not the neural arches, were doubled from the axis to T8. There was one thyroid gland and one larynx and hyoid apparatus. The two tongues were joined at their base just rostral to the single epiglottis. The palate was completely split in the right head but only partially split in the left. The cranial nerves were normal and doubled except for IX, X and XI. The brains were fused at the pons-medulla junction. An anomalous midline tag of neural tissue resembling remnants of the medial halves of two nervous systems extended from this point to the level of T8. Possible developmental mechanisms and rates of incidence are discussed.
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  • 39
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Fusion of the cervical spine in Globicephala macrorhyncha is a prenatal rather than postnatal phenomenon which encompasses all cervical vertebra. This results in a relatively short, nonarticulated, composite cervical spine in this particular species. Cervicothoracic spine segments removed from fetuses demonstrated complete fusion of all cervical vertebra commencing during early prenatal development. C1 and C2 initially developed as a composite central cartilaginous unit, although laterally there was some separation through rudimentary interzone formation. However, C3 through C7 formed individual cartilaginous centra which were divided from each other by thin, well-demarcated interzones, but without the formation of intervertebral discs (which were concomitantly evident dividing the thoracic, lumbar, and caudal vertebra, and were also present between the seventh cervical and first thoracic vertebra, although this was a very rudimentary intervertebral region). The first primary ossification center appeared in C2. Subsequently, primary ossification occurred in C7, and finally in C2 through C6, with ossification progressing in a craniocaudal fashion in these four vertebra. The centra ossification centers then progressively coalesced in the midline, from C2 to C7, in a craniocaudal sequence. This entire chondroosseous fusion process was completed during early gestation (probably less than 2 to 3 months of prenatal development), so that a composite “single” cervical vertebra developed that characterizes this species at birth and throughout postnatal development. Postnatally, ossification spreads laterally within each centrum, and also progressively removes the vestiges of the intervertebral material. C7 also develops a secondary ossification center, but only in the caudal region. The cranial end of C7 and the remainder of the cervical vertebra do not form secondary centers. An extensive fibrocartilaginous/hyaline cartilage bridge remains between C1 and C2, even after closure of the vertebral physes. Undoubtedly, this allows continued growth in C1 and C2, which become the dominant portion of the cervical unitary vertebra. Eventually, even this synchondrosis will disappear to form a completely osseous cervical mass.
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  • 40
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    The @Anatomical Record 200 (1981), S. 103-113 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Capillary density and capillary orientation in canine spinal cords were estimated by calculating actual lengths, surfaces, and volumes of capillary segments in tissue sections. Transverse, sagittal, and frontal section planes were sampled from dorsal, ventral, and lateral funiculi and from dorsal and ventral gray horns of spinal segments C3, T6, and L3 from three dogs. Capillaries were defined as vessels less than 10 μm in diameter. Electron microscopy of 104 such vessels revealed no muscle coat but collagen fibrils between endothelium and astrocyte process in 68% of the white matter capillaries and 16% of those in gray matter. Capillary diameter was significantly different among regions in some cases, but consistent patterns of variation were not found. Capillary density was four to five times greater in gray matter than in white matter. Capillary density differed significantly among the same-size dogs, but within dogs, density was similar among segments and within gray matter and white matter regions. In 62% of the transverse sections, capillary orientation was significant but mean direction was variable. Significant capillary orientation was found in 89% of the sagittal and frontal sections, and the mean direction was always along the craniocaudal axis of the spinal cord. The craniocaudal orientation was significant in 96% of the white matter sections and 78% of the gray sections, and in 97% of the cervical and thoracic sections but only 73% of the lumbar sagittal and frontal sections.Because capillary orientation is neither isotropic nor regular, unbiased, lowvariance estimates of capillary density cannot be expected without resorting to excessive sampling. An efficient method of quantifying spinal capillaries for comparative purposes by counting number of profiles per unit area is recommended.
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  • 41
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    The @Anatomical Record 200 (1981) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 42
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    The @Anatomical Record 200 (1981), S. 121-125 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The central nervous system (CNS) of the pigeon has been difficult to fix with consistency, and consequently this problem has impeded ultrastructural studies of various parts of the pigeon brain. Here we describe a method for effective fixation of the pigeon CNS and discuss the three principal problems associated with good fixation of this animal's brain. The animal was deeply anesthetized and the thoracic cavity was opened without collapsing the pectoral girdle upon the brachiocephalic trunks and the common carotids. The perfusion pressure was raised to 140-150 mm Hg to overcome the high resistance of the small diameter, long common carotids. Heparin was added to the wash buffer to retard coagulation of blood in the vascular bed of the brain. The method is not foolproof, but with care excellent fixation can be achieved.
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  • 43
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    The @Anatomical Record 199 (1981), S. 449-457 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The morphological features of avian epiphyseal cartilage have been investigated by freeze-fracture techniques. Progressive changes occurred in both the cells and the matrix during differentiation. Chondrocytes changed in shape from small flattened cells with few, short cellular processes, to enlarged ovoid cells with numerous long processes often associated with extracellular vesicles. In the matrix these vesicles appeared first in the cellular lacunae, then in the extralacunar matrix, becoming larger and more numerous. Large membrane-associated particles (MAPS) were seen on the p faces of the plasmalemma. These became progressively concentrated on and around the cellular processes, with few large MAPS being seen on the e face. Similar distribution of MAPS was seen in the matrix vesicles. Domains of hydrated proteoglycan aggregates were manifest as regular fracture patterns in the extralacunar matrix of the upper regions of the plate. Collagen fibrils progressively increased in size and state of aggregation, often being associated with matrix vesicles and in the end, with long plate-like mineral crystals. These findings, while in basic agreement with patterns observed with TEM, reveal important new features concerning cellular and matrix structure during cartilage differentiation.
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  • 44
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    The @Anatomical Record 199 (1981), S. 459-471 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Fibroblasts of the periodontal ligament (PDL) of the mouse exhibit a high degree of cytoplasmic and functional polarity. This polarity is dependent upon an elaborate system of microtubules. The location of the microtubular arrays and the observed effects of colchicine administration suggest that microtubules play an important role in maintaining the organization of the Golgi complex and its functional relationship to the rough endoplasmic reticulum. Smooth-walled intermediate vesicles, apparently derived from the rough endoplasmic reticulum, are aligned along microtubules at the immature face of the Golgi apparatus, and mature secretory granules are closely related to microtubules at the mature face of the Golgi apparatus. In distal cell processes the granules are closely parallel to microtubules and on occasion bridge-like attachments from granules to microtubules were noted. This relationship of secretory granules to microtubules, the lack of granule storage, and the effects of colchicine on granule secretion suggests that microtubules are part of a mechanism for collagen granule translocation from the Golgi complex to the cell periphery.
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  • 45
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 199 (1981), S. 473-480 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The purpose of this study was to assess the importance of the phagocytic mechanism of collagen resorption in the normal turnover and remodelling of soft connective tissues. Collagen phagocytosis by fibroblasts in rat skin, attached gingiva, and periodontal ligament was quantitated using the methodology of electron microscopic stereology. Periodontal ligament contained five and 15 times as much phagocytosed collagen as attached gingiva and skin respectively. Also, for each tissue examined, a positive correlation was observed between the amount of collagen phagocytosed and the known rate of mature collagen turnover.
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  • 46
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    The @Anatomical Record 199 (1981), S. 481-489 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The present study defined the ultrastructural features of peritubular capillary development. Two-day-old beagle puppies and adult dogs were perfused with 2.5% glutaraldehyde and routinely prepared for light and transmission electron microscopy. Some of the fixed tissue was subsequently used to make freeze-fracture replicas.The outer cortex of the puppy kidney possessed large, thick-walled vessels best termed sinusoidal capillaries instead of the small caliber vessels (peritubular capillaries) noted in the adult. These sinusoidal vessels showed extensive overlapping of the endothelium with isolated patches of fenestrae. Their luminal surfaces were irregular, owing to prominent ridges and sporadic bulges of endothelium. The basement membrane of most vessels was not present. Interstitial spaces were filled with mesenchymal cells and cells closely resembling pericytes. The diameter of the fenestrae of vessels throughout the cortex was similar; however, the number of fenestrae per micrometer of endothelium increased significantly from outer to inner cortex. Vessels of the inner cortex were also immature when compared to the adult. From these morphological findings, it was apparent that a true peritubular capillary system does not exist in the two-day-old puppy. Ultrastructural features of these vessels suggested reduced permeability characteristics.
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  • 47
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    The @Anatomical Record 199 (1981), S. 491-505 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A study of the circadian rhythm in the mitotic index (MI) of the corneal epithelium was completed in non-tumor-bearing mice and in mice bearing the Ehrlich ascites carcinoma (EAC). All mice were standardized to a light-dark cycle with 12 hours of light from 0600 to 1800 CST alternating with 12 hours of darkness from 1800 to 0600 CST. Treatments included injection with saline (SAL) or hydroxyurea (HU) at different circadian times. This investigation demonstrated that: (1) Data from untouched animals cannot serve as proper controls because treatment with SAL altered the level of the MI, but only during the diurnal, not the nocturnal, phase of the circadian cycle; (2) the presence of the EAC depressed the level of the MI, but this inhibition was only detected during the diurnal period; (3) treatment with 500 mg/kg HU injected at 0500 caused more perturbation in this rhythm than did treatment with 500 mg/kg HU at 1700; (4) when 500 mg/kg HU was given at 2000 and 0100 and 0500, the perturbation of the rhythm was greater than when 500 mg/kg HU was given at 0900 and 1400 and 1700; (5) when 3000 mg/kg HU was given at 1700 and compared to 500 mg/kg HU at 1700, little difference in the overall circadian profiles of these rhythms was observed, indicating that the circadian control mechanisms operating on the MI exerted a greater influence than did a dosage change from 500 to 3000 mg/kg HU; and (6) a comparison of the practice of plotting experimental and control data as “hours after treatment” versus using a “time of day” plot for the same data demonstrated that the “hours after treatment” plot is very misleading because it fails to account for the significant circadian oscillation in this in vivo system.
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  • 48
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    The @Anatomical Record 200 (1981), S. 207-220 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: ABSTRACT Recently, the deep cortex of the adult rat lymph node was shown to be made up of semirounded lymphocytic “units.” Each unit is contiguous to the peripheral cortex, bulges into the medulla, and is centered on the opening(s) of an afferent lymphatic vessel of a node. Furthermore, each unit comprises a “center” and a “periphery,” bearing distinct morphological features. The present study investigated the postnatal development of the units in rats of various ages. One minute after birth, no lymphocytic structures were detected in the nodes. One day after birth, tiny rounded lymphocytic areas were detected in the developing cortex. These areas were topographically related to the openings of afferent lymphatic vessels. One week after birth, small semirounded lymphocytic areas with some morphological features of the adult deep cortex units were observed. Two weeks after birth, typical units were present in the nodes. The observations indicated that the rounded lymphocytic areas observed in nodes of rats aged 1 week or less were actually developing deep cortex units. The overall findings further provided information on the morphological processes involved during the postnatal development of the deep cortex units. Key words: lymph node, deep cortex, development of deep cortex, rat.
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  • 49
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    The @Anatomical Record 200 (1981) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 50
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    The @Anatomical Record 200 (1981), S. 231-237 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A morphometric analysis has been done on developing rat substantia gelatinosa of the lower cervical and upper thoracic levels of the spinal cord starting on the 15th day of gestation. The following parameters were measured: cell body diameter, cytoplasmic/nuclear areas, synaptic density, synaptic type and vesicle morphology of the presynaptic terminal in axodendritic synapses. Cell body size and cytoplasmic/nuclear areas of gelatinosal cells increase until the 15th day postnatally and then decrease somewhat to the adult values. The first synapses are seen on gestation day 17. Synaptic density increases linearly until the third day postnatally. Axodendritic synapses are most common throughout development and in the adult, while the proportion of axoaxonic synapses increases and axosomatic synapses decreases during development. Most of the terminals in axodendritic synapses contain clear-spherical vesicles but the occurrence of clear-flat vesicles and dense-cored vesicles in the terminals increases during development. It appears that these morphological parameters provide a stable index of development in the substantia gelatinosa which can be correlated with functional development of the area. Hopefully, they will provide a means to assess subtle anomalies induced by nonteratogenic drugs or other environmental changes.
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  • 51
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    The @Anatomical Record 201 (1981), S. 43-49 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: There have been advances in electrophysiology which have necessitated a more thorough semi-quantitative analysis of the entire conduction system to yield data useful for correlation purposes. Thus an attempt is made to modify and expand our previous method of studying the conduction system pathologically. This method thus includes the study of the sinoatrial (SA) node and its approaches, the atrial preferential pathways, the approaches to the atrioventricular (AV) node, the AV node, the penetrating and branching portions of the AV bundle, the bundle branches, the peripheral Purkinje nets, and the remainder of the atrial and ventricular myocardium.The SA node and its approaches are studied in a longitudinal manner. This gives a better insight into the pathologic changes than does a study in the transverse direction. The approaches to the AV node, bundle and bundle branches are studied in an oblique manner, rather than horizontally apicalward, or from the posterior to the anterior septal region. The horizontal manner does not give sufficient sampling of the AV node and bundle unless complete serial sections are made. Sectioning from the posterior to the anterior septal wall makes difficult an evaluation of the right bundle branch.In conduction system correlation with Wolff-Parkinson-White and Lown-Ganong-Levine syndromes complete serial sectioning of both AV rims is advisable. Where complete serial sectioning is impossible in large adult hearts, retaining every fifth section may be permissable. In the study of congenitally abnormal hearts, it is advisable to embed the entire heart as a unit. If that is impossible because of the size of the heart, then very careful judicious planning of the fashioning of the blocks is necessary, so that displaced SA nodes, and anterior AV nodes and bundles are not overlooked.
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  • 52
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    The @Anatomical Record 200 (1981) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 53
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    The @Anatomical Record 200 (1981), S. 1-10 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Odontoblasts are cells with single cytoplasmic processes that grow longer as more dentin is elaborated. Ameloblasts also have single processes and it has been postulated that they too grow longer as more enamel is made. Support for this hypothesis was obtained using rat incisors to investigate the behavior of substances labeled with 3H-proline and 3H-fucose. A comparison was made between odontoblasts, which have processes known to grow and remain within the dentin, and the ameloblasts whose Tomes' processes are hypothesized to grow and leave remnants in the completed enamel. With 3H-proline, the odontoblast bodies are labeled at the early time intervals. They synthesize and secrete a layer of intensely labeled predentin, which by 1 and 2 days is converted to mineralized dentin. Matrix deposited after the main pulse is weakly labeled. Odontoblast processes are never labeled in dentin formed prior to injection. With 3H-fucose, the cell bodies are labeled at the early intervals and the newly formed glycoproteins are deposited into the predentin. Almost immediately, these are progressively added to the dentin at the calcification front. With time a gradient of labeling extends from the unlabeled dentin toward the odontoblast bodies. Unlike the behavior of labeled proteins, by 1 and 2 days labeled glycoproteins appear along the entire length of the odontoblast processes. In the enamel, no Tomes' processes are present during maturation. With 3H-proline, reactions are adjacent to the cells and diffuse toward, but do not reach the dentino-enamel junction by 1 and 2 days. With 3H-fucose, reactions appear over the enamel near the cells. By 1 and 2 days no diffusive pattern is seen, but grains are concentrated near the dentino-enamel junction, in a region containing holes known to be the beginning of Tomes' processes. Since odontoblast glycoproteins migrate along odontoblast processes, it was postulated that cytoplasmic remnants were present in enamel along which ameloblast glycoproteins could also migrate to reach the holes at the dentino-enamel junction.
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  • 54
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    The @Anatomical Record 200 (1981), S. 281-285 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Neural structures containing gonadotropin-releasing hormone (GnRH) in the bovine brain and infundibulum were characterized by light microscopic immunohistochemistry. GnRH-positive perikarya were localized singly or in small groups within the infundibular nucleus and were seen grouped in large discrete clusters within the ventromedial nucleus. Positive axons were localized within the brain from the nucleus of the rostral commissure to the medial mammillary nuclei, and in specific areas of the infundibulum and infundibular stalk.
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  • 55
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    The @Anatomical Record 200 (1981), S. 115-120 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The effects of melatonin and cooling on the disintegration and reassembly of microtubules were studied in the sciatic nerve of the toad. Control and melatonin-treated nerves showed disintegration of the majority of microtubules after 2 hours of cooling. When room temperature was restored, microtubules were reformed in the controls, but not in the nerves treated by melatonin where the disorganization persisted. These results demonstrate that melatonin interferes with the microtubular reassembly after cooling of the axons of the sciatic nerve.
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  • 56
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    The @Anatomical Record 200 (1981), S. i 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 57
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    The @Anatomical Record 200 (1981), S. 127-137 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Histochemical properties, muscle fiber cross-sectional area, muscle fiber length, and the oxidative capacity of masticatory muscles of female rhesus monkeys were assessed following alteration in functional length by an intraoral appliance or by detachment of the muscle. Experimental groups received the appliance only (A); the appliance and subsequent detachment of the masseter (AD); the appliance and detached masseter, but with surgical reattachment of the masseter to the pterygomasseteric sling (ADR); no appliance, but detachment and reattachment of masseter (DR); or an appliance which was removed after 24 weeks to study posttreatment responses (PT). Animals were sacrificed and the muscles were studied at intervals from 4 to 48 weeks after initiation of the experimental period. The results of these studies led to the following conclusions: (1) Stretching the masseter and temporalis muscles within physiological limits did not significantly alter the proportion of fiber types, although oxidative capacity of the fibers was reduced. (2) Fibers with “intermediate” myofibrillar AT-Pase activity were no more prevalent in experimental than control muscles. (3) The cross-sectional area of Type I fibers of masseter muscles decreased following some experimental procedures, indicating that recruitment of these fibers is the most sensitive to altered jaw function. (4) Minimal alteration of muscle capillarity was induced by any of the experimental procedures. (5) The lengths of masseter muscle fibers in Group PT and of temporalis muscle fibers in groups AD and ADR were greater than in control animals.
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  • 58
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    The @Anatomical Record 201 (1981), S. 573-576 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Medical students often find it difficult to conceptualize and learn the anatomy of the inguinal region and canal. A model of the inguinal canal, appropriate for lecture and laboratory presentations, has been used for many years by one of the authors (J.J.J.), and based on student and staff feedback, is judged a successful visual learning aid. This paper outlines a step-by-step procedure for constructing the model out of plexiglass and colored, felt-tipped marking pens.
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  • 59
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    The @Anatomical Record 201 (1981), S. 577-586 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Analysis of electon microscopic radioautographs revealed a maximum labeling with 3H-proline of rough endoplasmic reticulum (RER) at 3 minutes, Golgi saccules 1 and 2 at 10 minutes. Golgi saccules type 3 at 20 minutes, and presecretory and secretory granules at 30 minutes. Labeling of the extra-cellular collagen matrix occurred at 30 minutes and increased with time. These observations suggest that pro-a-chains of collagen in periodontal ligament fibroblasts are synthesized in the RER and transported to the Golgi apparatus within 10 minutes. These chains then undergo parallel alignment in Golgi saccules type 2 and form segment-long-spacing-like crystallites in Golgi saccules type 3 between 10 and 20 minutes. The peak labeling of presecretory granules and mature secretory granules in small amounts at 30 minutes and the rapid increase in labeling of extracellular collagen matrix which begins at 30 minutes, indicates that the formation of secretory granules requires approximately 30 minutes and that a rapid system of secretory granule translocation exists in periodontal ligament fibroblasts. This evidence futher supports the previously published morphologic evidence for a microtubuledependent system of collagen secretion in periodontal ligament fibroblasts (Cho and Garant, 1981b).
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  • 60
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    The @Anatomical Record 200 (1981), S. 337-347 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Utilizing Golgi-Cox impregnation, tanycytes were found in the ependyma of the cerebral aqueduct of the neonatal and adult rabbit. These tanycyte somas showed a variety of shapes, apical projections into the aqueduct, and basal processes (shafts) projecting into the mesencephalon, particularly into the periaqueductal gray (PAG). The shafts showed a variety of branching patterns, and sometimes abutted or terminated on capillaries or on specific neuronal elements. Other shafts coiled within the PAG or terminated within the neuropil of the mesencephalon. It is possible that these tanycytes provide a route for transport of cerebrospinal-fluid-borne substances from the aqueduct to the neuronal regions and vasculature of the mesencephalon. The presence of these tanycytes with complex branching patterns in proximity to neural and vascular structures suggests a permanent, active role for these specialized ependymal cells.
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  • 61
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    The @Anatomical Record 200 (1981), S. 349-356 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: We have developed and employed a stereotaxic coordinate system for the pig brain based on external skull landmarks. Sagittal, coronal, and horizontal planes were defined. Based on histological maps and ventricular casts, the coordinates for locating the lateral ventricles were described. Guide tubes leading to the lateral ventricles have been chronically implanted. This access route to the ventricular system has been used for stimulation of the dipsogenic response with angiotensin and for withdrawal of cerebrospinal fluid. Solved and unsolved problems arising with these procedures have been defined.
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  • 62
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    The @Anatomical Record 200 (1981) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 63
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    The @Anatomical Record 201 (1981), S. 273-281 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: An improved method is presented for processing single cells for electron microscopy. Agarose, which has a low (30°C) gelling temperature, was used as an initial embedding medium for single cells (spermatozoa and oocytes) and dissociated cell preparations (luteal cells and spleen cells). Dispersed cells of corpus luteum, spleen, and epididymal spermatozoa were placed in 1.5% agarose after aldehyde fixation. These fixed cells, embedded in agarose, were packed into a dense pellet by centrifugation, postfixed, then embedded in Epon. Mammalian eggs were not centrifuged; instead, they were embedded in agarose discs. Cells embedded in agarose were cooled below 30°C to allow for gelling, then processed for electron microscopy. Because agarose has a low gelling temperature, some heat-labile substances were preserved, as demonstrated by retention of peroxidase activity using the DAB histochemical method. The agarose embedding procedure is both rapid and facile, and has proven to be of value in the handling of fragile single cells for electron microscopic studies.
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  • 64
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    The @Anatomical Record 201 (1981), S. 293-302 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The muscle-tendon junctions of the extensor carpi radialis longus and brevis muscles from adult Balb C Bailey/J mice have been examined tensiometrically and ultrastructurally following removal of cellular membrane and soluble cytoplasm by exposure to nonionic detergent. As judged by the ability of the extracted muscle to generate tension upon exposure to ATP and to transmit the generated tension to the tendon, detergent extraction leaves the muscle-tendon junction functionally intact. Electron microscopic analysis of the extracted muscle-tendon junctions reveals that the relationship between the terminal myofilaments and the lamina densa of the basal lamina is retained, despite the extensive extraction of the plasma membrane. Fine filaments (2-7 nm) are seen to connect the lamina densa with an electron-dense intracellular layer into which terminal actin filaments appear to insert. These fine filaments are considered to represent an important component of the structural linkage between myofilaments and connective tissue and hence to be a significant component of the tension transmitting mechanism. Their precise nature is not known, but some part of the filaments must pass through the hydrophobic compartment of the plasma membrane and thus must be a transmembrane component of considerable tensile strength. These studies suggest that detergent-extractable membrane lipids play no significant role in the transmission of tension at the muscle-tendon junction, and that fine filaments, probably protein, are responsible for transmitting tension from myofilaments, through the plasma membrane, to the lamina densa of the basal lamina.
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  • 65
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    The @Anatomical Record 201 (1981), S. 553-561 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: In preceeding studies, we clarified the histology of the deep cortex of the rat lymph node. It was shown that the deep cortex is made up of basic elements termed “deep cortex units,” some of which are fused to one another into “deep cortex complexes.” Each unit is a semirounded lymphocytic structure, centered on the opening of an afferent lymphatic, contiguous to the peripheral cortex, and bulging into the medulla of a node. Moreover, each unit comprises a “center” and a “periphery,” bearing distinct morphological features. The present work was undertaken to verify whether the histology of the deep cortex of nodes from various species of mammals, currently used for experimental immunology, is comparable to that of the rate. The observations yielded a positive answer to the question.
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  • 66
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    The @Anatomical Record 201 (1981), S. 563-566 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: For identification of paraganglia (PG), samples of para-aortic tissue, tissues containing the coeliac-mesenteric ganglion complex, and the hypogastric ganglia were removed from 3- and 33-month-old male Fischer-344 rats and were processed by the formaldehyde-induced fluorescence method for visualization of catecholamines. Small PG containing 5-30 cells per section were found consistently in young animals. In each of six old rats, large PG containing 500-4000 brightly fluorescent cells per section were detected. Cell counting revealed a 13.5 × increase in number of PG cells between 3- and 33-month old rats. Microspectrofluorimetric quantitation in old rats showed equal amounts of catecholemines in PG cells and in adrenal medullary cells. Most PG were located in samples from the para-aortic area.
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  • 67
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    The @Anatomical Record 201 (1981), S. 567-572 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The authors observed the postaortic left innominate vein, which passed behind the ascending aorta, in the body of a 69-year-old Japanese male during dissection in 1979. In this case, no rudiment of the ordinary left innominate vein could be found in front of the arteries arising from the arch of the aorta. There are few reports of this anomaly and an extensive search of the available literature revealed only ten cases, including three in Japan. Adachi classified the postaortic left innominate vein into two types, types I and II, on the basis of the positional relation between the left innominate vein and the ligamentum arteriosum. Our case was of type I, in which the left innominate vein passed ventral to the ligamentum arteriosum and ran across from left to right behind the ascending aorta to join the right innominate vein. The embryological explanation which generally is accepted for the postaortic left innominate vein lies in the transposition of a transverse connection, which becomes the left innominate vein in a later stage of development, between the left and right anterior cardinal veins from the ventral to dorsal sides of the rudiment of the ascending aorta.
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  • 68
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    The @Anatomical Record 201 (1981), S. 537-551 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Rat adrenals in different states of stimulation were examined by transmission electron microscopy following perfusion fixation using an in situ isolated-circulation technique. In unstimulated glands, intracortical capillaries were constricted and the cells of the cortex were pressed closely together with little development of filopodia or intercellular spaces. Glands fixed during the period of operative stress, or following a 1 hr perfusion with Adrenocorticotropic hormone (ACTH) showed that the radially orientated capillaries of the cortex were massively expanded, and the cells of both the glomerulosa and fasciculata exhibited an extensive development of filopodia on their surfaces. These filopodia extended into enlarged intercellular spaces, where they often entered into complex relationships with filopodia from neighboring cells.The development of filopodia by cells of the adrenal cortex was also observed using scanning electron microscope techniques. In cells either icubated with ACTH in vitro or isolated from adrenals of rats treated with ACTH in vivo, the filopodia were numerous, often branched, and could reach as much as 1 μm in length. In contrast, adrenal cells obtained from animals pretreated with cortisol were smooth surfaced.Other cell characteristics, including mitochondria, smooth endoplasmic reticulum, dense granules, and coated vesicles did not show such dramatic correlations with the state of stimulation. It is considered that the development of filopodia and intercellular space is related to secretory mechanisms in the rat adrenal cortex.
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  • 69
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    The @Anatomical Record 201 (1981) 
    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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  • 70
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    The @Anatomical Record 199 (1981), S. 15-22 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The purpose of this study was to examine the distribution and mobility of anionic sites on the surface of fetal trophoblast in contact with maternal blood using polycationic ferritin (PCF) as a probe. Pieces of human placental villi were washed to remove maternal blood, and fresh, unfixed tissue was expose to PCF for varying times, concentrations, and temperatures to determine the effects on labeling patterns. The major findings were: (1) anionic sites were localized almost exclusively on the microvillous portion of the trophoblast surface; intermicrovillous regions of the surface, including the coated pits, were generally not labeled with PCF; (2) PCF binding was present as small clusters on the microvilli. This pattern was observed in tissue incubated 5-10 sec at 4°C and 23°C. The size of the cluster was increased with increased incubation time, suggesting some aggregation or patching can occur; (3) following the fomation of patches, the anionic sites showed no evidence of being cleared from the membrane by endocytosis during incubation subsequent to labeling; (4) the binding of PCF to the surface was reduced by pretreatment of the tissue with neuraminidase. Tissue fixed in glutaraldehyde prior to PCF exposure showed both clustered and more dispersed labeling. The results indicate that anionic sites on human trophoblast surface have a non-random distribution and have restricted mobility on the surface. This may be indicative of a segregation of different membrane proteins and functions within different structural regions of the placental cell surface.
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  • 71
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    The @Anatomical Record 199 (1981), S. 23-31 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: We have investigated morphologic and histochemical characteristics of serotonin-containing epithelial cells in tracheas from adult rabbits, using the Falck-Hillarp freeze-dried formaldehyde vapor technique. An intracellular formaldehyde-induced fluorescent substance was identified as serotonin by microspectrofluorometric techniques. Fluorescence microscopy and subsequent histochemical staining of the same sections demonstrated that serotonin-containing cells were argentaffin-, argyrophil-, and ferric ferricyanide-positive. The serotonin-containing epithelial cells were more numerous in ventral than in dorsal aspects of trachea. The number of detectable fluorescent cells was reduced after reserpine administration but was not affected by injecting the amine precursor L-dihydroxyphenylalanine (L-DOPA). The emission peak of the fluorophore was not significantly shifted after L-DOPA injections. The cells may regulate tracheobronchial-pulmonary function by releasing serotonin or other as yet unidentified biologically active substances.
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  • 72
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    The @Anatomical Record 199 (1981), S. 45-59 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Diagrams of the lymph node currently represent its deep cortex (paracortex) as a layer of rather uniform thickness underlying the whole peripheral cortex. However, this concept has not been supported by actual observations; previous nvestigators have observed, instead, related structures whose appearance varied greatly from nodule-like to ill-defined components. Clearly, the present knowledge of the histology of the deep cortex is inadequate and confusing. Therefore, we undertook a tridimensional study of the region in different nodes of rats. The present work, bearing on the topography of the region, revealed that the deep cortex of the rat node is formed of one to several basic “units”. Each unit is a semi-rounded structure, varying from semispheric to semi-ovoid in shape and contiguous to a portion of peripheral cortex. The work further showed that two to several units can fuse to form a “complex”. The data indicated that the number, the size and the shape of the units and/or of the complexes of a node differ to some extent according to its anatomical location. These differences probably reflect corresponding variations in the nature and importance of the antigenic stimulation in the different sites of the organism. Finally, the study demonstrated the necessity of tridimensional examination of a node to obtain adequate information on its overall architecture and, particularly, on its deep cortex topography.
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  • 73
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    The @Anatomical Record 199 (1981), S. 321-339 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A comparison of the anatomy, fiber type profiles, and contractile properties of the wrist flexor muscles was undertaken in the cat. Isometric contractile characteristics were measured for each muscle. Three muscle fiber types, FG, FOG, and SO, were differentiated by staining cross sections of each muscle for ATPase, NADH diaphorase, SDH, and α-GPD activities. The wrist flexor muscles ranged from less than 1% to 49% SO fiber content; with two of the five heads of the flexor digitorium profundus (FDP) having 1% or less SO fibers (FDP1 - 1.07%, FDP5 - 0.81%) and the humeral head of the flexor carpi ulnaris muscle (FCUh) having the greatest content of SO fibers. The mean contraction time (CT) plus one-half relaxation time for an isometric twitch was correlated with the percentage of SO fibers and ranged from 40.5 to 111.8 ms. Except for the FCU (37 ms), the CT was less than 25 ms for the wrist flexor muscles. The uniarticular wrist flexor muscles, the flexor carpi radialis (FCR), and the FCU had the highest percentage of SO fibers and were more fatigue-resistant that the multiarticular muscles. Considerable differences exist in muscle structure, fiber type proportions, and contractile properties between the FCR and FCU, which may be related to functional differences between the two sides of the wrist that may exist during the placement of the foot during locomotion.
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  • 74
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    The @Anatomical Record 199 (1981), S. 309-320 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The formation and maturation of collagen secretion granules in periodontal ligament (PDL) fibroblasts of young male Balb-C mice were studied by electron microscopy and cytochemistry. The Golgi apparatus was composed of several dictyosomes, each consisting of a stack of five smooth-walled cisternae. Each cisterna was connected at both ends to a dilated saccule. The cisternae, with their associated pairs of saccules, underwent progressive maturational changes from the immature to mature face of each dictyosome. The most immature saccules (type 1) were large, spherical, and filled with loosely arranged short filamentous structures. These saccules were continuous with the first and second Golgi cisternae (counting from the immature side). Golgi saccules type 2 were ellipsoidal, associated with the third and fourth cisternae, and contained parallel, elongate filaments. The most mature saccules, type 3, were more rectangular and connected by a short fifth cisterna. They contained aggregated filamentous material in the form of eight segment-long-spacing (SLS)-like crystallites, one in the center and seven at the periphery, to form a basic secretory unit. As type 3 saccules matured, the interconnecting cisterna progressively shortened until the two saccules were nearly juxtaposed. At this time the shortened fifth cisterna split to give rise to two independent presecretory granules. By progressive condensation, presecretory granules matured into secretion granules that contained a densely packed SLS- like aggregate, within which individual crystallites were no longer discernable. Maturation of cisternae and saccules involved removal of membrane, apparently by the formation and detachment of coated vesicles. The staining reaction with silver methenamine and phosphotungstic acid increased over the procollagen as the saccules matured, indicating addition of carbohydrate moieties and possible crosslinkages. It is concluded that the formation and maturation of collagen secretion granules in PDL fibroblasts involves the packaging and further modification of eight SLS-like crystallites, which are secreted as a basic unit.
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  • 75
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    The @Anatomical Record 199 (1981), S. 349-360 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The establishment of the undifferentiated gonad was studied in Xenopus laevis and Rana pipiens using high resolution techniques. It was found that the cells of the so-called “mesonephric blastema” had no structural resemblance to the cells of the gonadal medulla in both species. Furthermore, there was no morphological evidence that would suggest a migration of the former cells towards the incipient gonad at the time of its appearance. However, the basal lamina of the coelomic epithelium was interrupted in the region of the genital crest, and there was a definite ultrastructural similarity between the cells of this epithelium and those that first form the medulla. These observations suggest that, in amphibians, the cells of the gonadal medulla come from a cellular line arising from the coelomic epithelium and not from the “mesonephric blastema,” as has been proposed.
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  • 76
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    The @Anatomical Record 199 (1981), S. 361-376 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Membranes of boar spermatozoa from different regions of the epididymis and after ejaculation were studied by the freeze-fracture replica technique. The ordered pattern of the intramembranous particles of spermatozoan plasma membranes was different in the five arbitrary zones of the epididymis and in the semen. A distinctive ordered pattern was absent in zone 1, which is the proximal segment of the epididymis. In zone 2, paired parallel rows of the particles were present in the plasma membrane over the acrosomal region. This parallel arrangement was not present in zone 3 spermatozoa. Anterior to the posterior ring, cords formed by packed particles were apparent in zone 2 spermatozoa and reached their maximum prominence in zone 3, and persisted in zones 4 and 5 and in the semen. The plasma membrane over the marginal ridge of the acrosome had a hexagonal array of particles only in zones 4 and 5 spermatozoa. A similar pattern appeared on the post-acrosomal region of spermatozoa in zone 5 and in the semen. The plasma membrane of the middle piece had a rectilinear arrangement of the particles in zone 2 spermatozoa in which the migration of the cytoplasmic droplet was complete. Rudiments of the rectilinear arrangement persisted in spermatozoa in zones 4 and 5 and in the semen. These changes are discussed in relation to sperm maturation in the epididymis. The acrosomal membrane had a hexagonal arrangement of particles in the equatorial segment. The marginal ridge of the outer acrosonal membrane had parallel rows of intramembranous particles. The organization of the acrosomal membrane particles did not change during the epididymal passage of boar spermatozoa.
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  • 77
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    The @Anatomical Record 199 (1981), S. 377-387 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The development of the secretion granule population of rabbit parotid glands after isoprenaline (IPR)-induced degranulation has been analyzed at the E.M. level using stereological techniques. Young male New Zealand White rabbits were sacrificed 2, 4, 8, 12 and 16 hours after IPR administration and the granule populations compared with those of starved controls. In controls. In control glands a third of cell volume was occupied by stored secretory material, and it was estimated that, on average, cells contained 386 granules. The granule population as a whole had a mean diameter of 0.94 μm, with a unimodal positively skewed size distribution. Two hours after IPR treatment overall granule volume density was only 15% of that of control glands, but there was evidence that the process of restitution had already begun. At 8 hours about a fifth of acinar cell volume was occupied by electron-dense granules with an estimated mean diameter of only 0.58 μm, and the population as a whole was more strongly skewed than in the controls. In the later stages of restitution (12 and 16 hours), the volume of stored secretory material continued to rise, mean granule diameter increased, the size-frequency distribution became less skewed and the estimated number of granules per cell fell to 277 by 16 hours, suggesting that some granule fusion occurs during development.The analyses are discussed in relation to the techniques employed, and the results are equated with other independent evidence of the mode of granule genesis.
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  • 78
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    The @Anatomical Record 199 (1981), S. 389-401 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Recently weaned male rabbits were injected either with 150 μg/kg isoprenaline in saline containing 0.01 M ascorbic acid or simply with the drug vehicle. Groups of drug-injected animals were killed at various time after injection. Parotid gland tissue samples from all animals were fixed, embedded and thin sectioned, and micrographs were prepared at standard magnification. Estimations of membrane areas of each membrane type in parotid acinar cells were made. It was found that in animals killed 2 hours after induced secretion apical area was larger than in controls. In animals killed at sucessively later times the apical area was progressively less. No elevation of any internal smooth membrane areas was ascertained at any sampling time, though the areas of rough endoplasmic reticulum in 2-12 hour samples were larger. It is suggested that excess apical membrane, though probably removed by interiorization, is afterwards disassembled inside the cell to create fresh macromolecular building units (protein molecules), perhaps after passing through the Golgi apparatus. This cryptic pool of building units can provide about 900 μm2 of secretion granule membrane per cell, the supply apparently being exhausted in the first eight hours after degranulation, whilst granule numbers are being increased. Thereafter, apparently, limited granule fusion occurs, so that ultimately the cellular complement of secretion granule membrane comes to enclose a greater volume of secretory product, though the average granule number per cell is smaller.
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  • 79
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    The @Anatomical Record 199 (1981), S. 565-574 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Methods are described for the isolation of intact intestinal epithelium in several novel forms. The first method described is for application to segments of bowel that must be studied without killing the animal, e.g., a resected length of bowel. In this method, the isolated segment is everted onto a glass rod and incubated at 37°C in fresh 30 mM ethylenediaminetetraacetic acid (EDTA) in calcium-magnesium-free Hank's balanced salt solution (CMF) for either 15 or 20 minutes. At the end of the incubation, the epithelium is isolated by vibration into a tube of cold CMF. If it is incubated for 20 minutes, the entire epithelium is isolated in the form of single crypt-villus units. If it is incubated for 15 minutes, the epithelium is isolated in the form of small intact sheets, but not all of the epithelium is removed.The second method requires the death of the animal but yields better results. The anesthetized animal is perfused through the left ventricle with a fresh 37° solution of EDTA (0.01-30 mM) in CMF. Then the segment of gut is removed, everted onto a glass rod, and the epithelium isolated by vibration into cold CMF. The whole of the epithelium is isolated with this procedure and, with higher concentrations of EDTA, it is isolated in the form of large sheets (1-2 cm2). Structurally inact units could be obtained with either procedure. There was no contamination with underlying nonepithelial elements.The best results, as determined by morphology and viability, were obtained with the perfusion method using 30 mM EDTA. With this concentration, the whole procedure, from sacrifice of the animal to isolation of the epithelium, requires less than 4 minutes. Procedures are also described for the isolation of either pure intact crypts or of pure intact vill from small intestine. Each of the methods described could be used to isolate the epithelium from any region of the intestinal tract with equal ease. Some applications of the methods are also discussed.
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  • 80
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    The @Anatomical Record 200 (1981), S. 11-31 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Three-dimensional reconstructions of “regenerating” myotubes in the “degeneration-regeneration” regions and in the “regenerative” foci of the extensor digitorum longus muscle of the C57BL6J/dy2J myopathic mutant mouse were made from spaced serial ultrathin section. Complex branching and recombination occurred, involving myotubes which for extensive regions along their length appeared to be independent. No accumulation of specialized organelles occurred at the branching site. Continuous branches displayed multiple discrete motor endplates.
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  • 81
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    The @Anatomical Record 200 (1981), S. 447-459 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The purpose of this study was to determine the organization of collagen in the wall of the human pulmonary alveolus. Samples of human lung obtained at surgery were processed for light and electron microscopy. Light microscopy confirmed the general findings of Orsos ('36): there were 3 common fibers called primary, secondary, tertiary in this study in order of their increasing size. Primary fibers (called “pericapillary” by Orsos) formed a continuous mesh in the alveolar wall and were often confluent within the intercapillary regions of the wall (“knötenpunkten,” or nodes, Orsos). The tortuous secondary fibers (“circulatory fibers,” Orsos) passed frequently across the thickness of the alveolar wall and were closely applied to capillary walls. Tertiary fibers (“respiratory fibers,” Orsos) were continuous with the alveolar ostia and formed the supportive struts of the alveolar wall as they crossed the wall in a more direct course than the serpiginous secondary fibers.Electron microscopy (serial sections and stereo pairs) showed that the primary fibers inserted near the edge of an intercapillary region, where they were attached to the endothelial or epithelial basal lamina directly or by a smaller fiber or microfibril resembling the fibrous component of elastin or oxytalan. Primary fibers passed through a typical intercapillary region while describing a helix or a portion thereof. Secondary fibers were more coarse than primary, and both secondary and tertiary fibers resembled woven ropes.
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  • 82
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    The @Anatomical Record 200 (1981), S. 461-470 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: C-cell complexes are special cell groups consisting of a mass of C-cells associated with other epithelial elements and cysts. They are remnants of ultimobranchial bodies retaining fetal characteristics. In the C-cell complexes there are follicular cells in various stages of differentiation, i.e., the cell clusters not yet organized into follicles, primordial follicles with small lumens and comparatively enlarged follicles storing plentiful amounts of colloid. They have a morphology similar to follicular cells of fetal thyroid glands and react to antiserum to 19S thyroglobulin. In order to determine whether or not the follicles in these complexes have the ability to incorporate radioiodine, autoradiography after a single injection of 125I was combined with immunoperoxidase staining using specific anti-calcitonin, anti-C-thyroglobulin, and anti-19S thyroglobulin antisera. The 19S-positive cells not yet organized into follicles did not take up radioiodine. Primordial follicles showed a heavy accumulation of silver grains over their follicular lumens storing new 19S thyroglobulin as colloid. Comparatively enlarged follicles revealed a strong autoradiographic reaction and their labeling patterns were identical with those of typical thyroid follicles. These results confirm that the follicles in C-cell complexes, as well as thyroid follicles, can incorporate radioiodine and are related to thyroid hormone synthesis. That is, functional thyroid follicles can arise from the ultimobranchial bodies.
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  • 83
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    The @Anatomical Record 200 (1981), S. 491-500 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The embryonic development of the albino rat pineal gland has been studied from day 13 of development until birth. The first pineal anlage appears as a midline evagination of the diencephalic roof, which soon adopts a tubular morphology. At 17 days, the disappearance of the pineal recess begins, along with the transformation of the gland into a solid organ. The latter is mainly achieved by an infolding and thickening of the dorsal recess wall, from which derives most of the future pineal parenchyma. Blood vessels are mainly derived from the vessels found in the dorsal surface of the pineal gland.
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  • 84
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    The @Anatomical Record 200 (1981), S. 471-479 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The blood and bone marrow of New Hampshire chicks were analyzed quantitatively from the time of hatch to 8 weeks of age. Hormonal bursectomy was performed by treating embryonating eggs on the 11th day of incubation with testosterone propionate (TP) which resulted in severe hypogammaglobulinemia and complete atrophy of the bursa of Fabricius. TP-treated birds exhibited some lymphocytopenia, reduced splenic weight, and lack of plasma cells in their bone marrow. The number of cells per milligram bone marrow was comparable in normal and TP-treated birds, falling in the range reported for laboratory rodents. The chick medullary hemopoiesis is characterized by the predominance of erythroblasts throughout early development; granulocytes and lymphocytes represent much smaller cellular compartments than in rodents. In the chick granulocytes tend to decrease after hatch, whereas in rodents they tend to increase. The normal chick shows a temporary increase in marrow lymphocytes after hatch, similar to that observed in some young rodents, but on a much smaller scale. Hormonal bursectomy did not prevent the development of a lymphocyte population in the bone marrow. These cells were fewer in TP-treated birds at hatch and at 4 weeks than in normal birds, but at 8 weeks of age normal and bursectomized chicks had comparable numbers of lymphocytes in their marrow. Although some lymphocytes in avain bone marrow may depend on the bursa of Fabricius for their development, a substantial proportion of bone marrow lymphocytes in the chick are bursa independent. The cell surface phenotype and site of origin of these cells remains to be investigated.
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  • 85
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    The @Anatomical Record 200 (1981), S. 481-489 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Morphology of guinea-pig thymic fragments was studied sequentially during in vitro organ culture by using light and electron microscopy and 3H-thymidine autoradiography. In culture the fragments became alymphoid. Thymic lymphocytes started to disappear first at the corticomedullary border, which gradually broadened, giving rise to alymphoid epithelial fragments. As the lymphoid cells disappeared the thymic epithelium began to transform into a keratinized squamous epithelium. The keratinization started in the cells surrounding the Hassall's corpuscles, causing the enlargement of the corpuscles and finally total keratinization of the cultured epithelial fragments. In autoradiographic studies cell proliferation could be observed in uncultured thymuses at the cortical pericapsular area. In cultured alymphoid fragments labelled cells were distributed diffusely in the epithelium. Later labelling was concentrated to epithelial cells transforming to keratinized epithelium. Ultrastructural studies similarly showed transformation of the epithelial cells to squamous keratinized epithelium. The observation support the view that Hassall's corpuscles are derived from the keratinized thymic epithelium and that their existence is connected to the normal function of the epithelium.
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  • 86
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    The @Anatomical Record 201 (1981) 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 87
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    The @Anatomical Record 201 (1981), S. 1-11 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 88
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    The @Anatomical Record 201 (1981), S. 13-21 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Previous studies have indicated that total nucleolar area and volume remain constant regardless of the number of nucleoli. The question remains whether this relationship is valid for mass. To answer this, total nucleolar mass values were obtained from nuclei of living mesothelial cells in culture possessing one to four nucleoli. The nucleolar mass was calculated using interferometry. The mean total nucleolar dry mass for cells with one, two, three, and four nucleoli was 40 × 10-12gm, 38.4 × 10-12gm, 39.1 × 10-12gm, and 41.4 × 10-12gm, respectively. These data suggest that on the average, each cell had approximately the same total nucleolar dry mass regardless of the number of nucleoli.In an additional study, interferometry was employed to reveal changes in nucleolar mass and concentration during a seven-hour period. It was concluded that the nucleolus is a dynamic organelle, with its total mass varying in time from an average 40 × 10-12gm with a mean concentration of 22.2gm/100cm3.
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  • 89
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    The @Anatomical Record 201 (1981), S. 23-29 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The cell bodies of neurons innervating a rat mandibular molar tooth were examined with respect to their location in the trigeminal ganglion. The study sought to determine if these cell bodies were restricted to a specific somatotopic location within the mandibular territory of the ganglion or if they were distributed throughout the entire mandibular territory. Horseradish peroxidase (HRP) pellets were placed in the cavity preparation of right first mandibular molar teeth for a 24-hour period. The animals were then perfusion fixed, and the right trigeminal ganglion was removed, sectioned and processed by the tetramethyl benzidine neurohistochemical technic.The four trigeminal ganglia constituting this experimental series demonstrated 129, 185, 236, 318 HRP-positive cell bodies. These cell bodies were dispersed throughout the extent of the mandibular territory. It was concluded from these observations that the distribution of cell bodies innervating a rat mandibular molar tooth is not restricted to a specific region of the mandibular territory of the trigeminal ganglion, but rather the distribution of these cell bodies is throughout all parts of the mandibular territory.
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  • 90
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    The @Anatomical Record 200 (1981), S. i 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
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  • 91
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    The @Anatomical Record 200 (1981), S. 253-258 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Ultrastructural studies of the stone crab (Menippe mercenaria) and the lobster (Homarus americanus) demonstrate that the basement membrane of the midgut (intestine) is unusually complex. In both species, the basement membrane is three-layered and has processes that form extensive networks protruding into the connective tissue. The possible functional significance of this complex structure is discussed.
    Additional Material: 6 Ill.
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  • 92
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 200 (1981), S. 259-270 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The histological structure of the gerbil Harderian gland was investigated by means of light and transmission electron microscopy. The single excretory duct of the gland is directly continuous with endpieces at the hilus and opens nasally and ventrally to the third eyelid. The excretory duct is accompanied by many acini of small serous glands around it. The gland is composed of tubuloalveoli (tubular alveoli) with wide lumina and is not divided into lobules. There is no branched duct system within the gland. The tubuloalveoli themselves convey the secretory materials to the hilus where the excretory duct begins. The alveolar epithelium is composed of only one type of glandular cell as well as myoepithelial cells. The glandular cells contain many clear secretory vacuoles containing lipids and well-developed tubular smooth endoplasmic reticulum. The secretory vacuoles are surrounded by a unit membrane and are secreted by exocytosis. The interstices of the gland contain two types of autonomic nerve varicosities and a number of melanocytes. The surface of the gland is covered with the endothelium of the orbital venous sinus.
    Additional Material: 12 Ill.
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  • 93
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    The @Anatomical Record 200 (1981), S. 41-59 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The ultrastructural organization of 40 soleus neuromuscular junctions from ten normal young adult male and female Sprague-Dawley (SD)-derived rats (Charles River Breeders, CD-Crl:COBS (SD)BR) has been studied. A smaller sample of motor endplates from the gastrocnemius, diaphragm, and extensor digitorum longus muscles of these rats as well as from the soleus muscles of two adult Wistar (W) rats (Crl:COBS(WI)BR) was included. Widespread ultrastructural reorganization was evident at the soleus neuromuscular junction during the growth period from three to five months of age. A major characteristic of reorganization is the presence of junctional folds not associated with axonal terminals; such sites occur within a single endplate adjacent to areas with typical intact synaptic associations. Additional features possibly related to remodelling are: (1) spatial separation of axonal terminals from the myofiber, (2) intervention of Schwann cell cytoplasm between an axon terminal and myofiber, (3) aggregates of satellite cells, and (4) folded or multilayered basal lamina. These features are most pronounced in the soleus muscle but occur to varying degrees in the neuromuscular junctions of other muscles of SD-derived rats.Distinctive characteristics of the rat soleus postjunctional sarcoplasm include the widespread occurrence of myofibrillar components, abundant free and membrane-associated polysomes, and triads oriented in various planes. Away from such discrete sites, myofibers possess the usual highly oriented organization of myofibrils, T tubules, sarcoplasmic reticulum, and mitochondria.The soleus muscle is a postural muscle that responds directly to rising workload imposed by continuous body growth during young adulthood by steady myofiber hypertrophy and conversion of motor units (Kugelberg, '76). This changing structural-functional relationship may be reflected also by ultrastructural remodelling of the neuromuscular junctions reported here.
    Additional Material: 12 Ill.
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  • 94
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 200 (1981), S. 67-81 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Buccopharyngeal epithelium covering gill arches and gill rakers of the fathead minnow was studied by light microscopic, scanning, and transmission electron microscopic techniques. Mature mucous cells in goblet pattern and nonmucus containing cells were in the apical one-third of the tissue. The latter cells contributed to a surface microridge system which overlapped apices of goblet cells. The bottom of the epithelium was comprised of a continuous row of darkly stained basal epithelial cells. In this region, two to three epithelial cells of similar staining characteristics were piled up forming apical columns which partially encircled nests of lightly stained cells. A basal lamina and thick basement lamella of about 20 plies of orthogonally arranged collagen supported the epithelium. Numerous taste buds were seen in gill arches and rakers. Taste bud cellular components included marginal cells, light receptor cells, dark receptor cells, and basal cells. These were identical in all taste buds. Taste bud surface morphology differed between gill arch and raker. Pores of the former were depressed, while those of the latter were raised. Thick microvilli of taste pores were apical extensions of light cells, while smaller, more numerous microvilli were projections from dark cells.
    Additional Material: 22 Ill.
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  • 95
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 200 (1981), S. 95-101 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The origin of the afferent fibers to the lingual muscles of the dog was investigated by means of retrograde transport of horseradish peroxidase (HRP) from injection sites in the tongue and the extrinsic lingual muscles. Intralingual injections were not satisfactory because the enzyme diffused beyond the intrinsic lingual muscles to include virtually all tissues within the tongue. Thus, the resultant retrograde labeling of cell bodies of the trigeminal, geniculate, glossopharyngeal, vagal, and first cervical (C1) spinal ganglia represented a composite of lingual sensory innervation.In order to confine HRP uptake to intramuscular nerve endings, injections were limited to surgically isolated extrinsic lingual muscles, i.e., the genioglossus, hyoglossus, and styloglossus. After these intramuscular injections, labeled neurons appeared ipsilaterally in the C1 spinal ganglion, the proximal vagal (jugular) ganglion, and trigeminal ganglion. Earlier suggestions that the lingual proprioceptive neurons of the dog reside in the distal vagal (nodose) ganglion and hypoglossal ganglia were not confirmed. The mesencephalic nucleus of the trigeminal nerve failed to label after enzyme injections into the tongue or the extrinsic lingual muscles.The retrograde labeling of cell bodies in the C1 spinal ganglion was abolished when HRP injections into the extrinsic lingual muscles were preceded by surgical interruption of the ansa cervicalis or distal section of the hypoglossal nerve. Retrograde labeling of neurons in the proximal vagal ganglion persisted after hypoglossal nerve transections.
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  • 96
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    The @Anatomical Record 201 (1981), S. 189-195 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The ependymal lining of the central canal of the filum terminale and spinal cord in the vicinity of the caudal neurosecretory system in P. sphenops was examined in this study. Two general cell types based on shape and location were observed in the ependymal lining: cuboidal ependyma located in dorsal aspects of the filum terminal and columnar to pseudostratified ependymal cells found in ventrolateral and ventral aspects of the filum terminale. Comparison of the ependymal lining was made in animals adapted to saltwater and freshwater. In animals adapted to saltwater there was an increase in the basal infoldings of the cell membrane of the dorsal cuboidal ependyma. Infolding of the basal cell membrane is a phenomenon shared by cells known to participate in transport of electrolytes. Since a possible functional relationship between the ependyma of the third ventricle and median eminence has been shown, in future studies on the osmoregulatory function of the caudal neurosecretory system the ependymal lining of the central canal in this region should be considered.
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  • 97
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    The @Anatomical Record 201 (1981), S. 179-188 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Mapping of atrial-AV nodal (AVN) activation patterns was performed in 10 superfused rabbit AVN preparations utilizing 3 bipolar electrodes placed simultaneously at the crista terminalis (CT), interatrial septum (IAS) and His bundle (H) regions in close proximity to the AVN, along with two or three microelectrodes in the AN, N and NH regions of the AVN. Basic and premature stimuli were introduced at either or both the CT and IAS regions of the AVN. The timing of the premature stimuli was varied to induce close interaction of inputs to the AVN. Summation and/or cancellation, as evidenced by changes in the morphology of the action potentials and alteration of H1-H2 intervals, were observed. Apparent reentry phenomena could be induced or terminated by appropriately timed stimulation at the CT and IAS inputs. Reentry was critically related to both the patterns and timing of the spread of excitation within AVN and surrounding atrial tissue. Slow conduction and unidirectional block were observed in various portions of the reentry circuit. It is concluded that (1) interaction between input waves engaging the AVN produced either summation or fragmentation; (2) slow conduction and reentry resulted from a critical collision of wavefronts: (3) in this preparation, AVN reentry circuits always appeared to involve conduction through atrial tissue immediately surrounding AVN; and (4) remarkably, reentry confined to the intranodal region was never observed.
    Additional Material: 5 Ill.
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  • 98
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 201 (1981), S. 225-235 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Urea and dithiothreitol can decondense the chromatin in some of rat sperm heads. By this treatment, we have observed that in the nuclei of rat sperm the chromatin is organized into two morphologically distinct portions, namely: the compact chromatin rods of about 450 to 1,000 Å thick, and the interlacing fibers about 250-290 Å in thickness. When these treated sperm are further digested with micrococcal nuclease, the small fibers disappear, whereas the chromatin rods are still present in the “urea-nuclease pellet.” From the available evidence, we suggest that the chromatin rods represent the highly packed nucleoprotamine, whereas the small fibers represent the more loosely organized nucleohistone.
    Additional Material: 7 Ill.
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  • 99
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 201 (1981), S. 203-223 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The relationship of nascent albumin and hepatocyte organelles was studied with the immunoperoxidase reaction in rats given various drugs to alter cellular albumin content. Colchicine was used to increase intracellular albumin. Cycloheximide inhibited synthesis but allowed nascent albumin to remain with its ribosome of origin. Puromycin also inhibited synthesis but released albumin from its ribosome. There was no difference in the appearance of attached ribosomes in hepatocytes from saline-injected rats and those given colchicine or cycloheximide. In these cases, membranes of the endoplasmic reticulum were consistently decorated with ribosomes positive for the presence of albumin antigenicity on their cytosolic surface. The cisternal and cytosolic compartments were negative. The situation after puromycin was different. Here the membranes appeared to be denuded of ribosomes and reaction product, indicative of albumin, was present only on the lumenal surface. To determine whether puromycin had caused the release of ribosomes, sections from puromycin-treated cells were stained nonspecifically with uranyl acetate. This showed that the normal amount of ribosomes was still bound but that they could not be seen when a probe specific only for albumin was used. It appears that nascent albumin can associate with its ribosome within the cytosol. Also, apparently after albumin passes through the membrane of the rough endoplasmic reticulum, it remains attached to its lumenal surface. A model incorporating cytosolic folding of albumin followed by its entropic membrane transit is presented.
    Additional Material: 33 Ill.
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  • 100
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    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 201 (1981), S. 237-248 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: We reinvestigated the still controversial existence of arterial pathways by-passing glomeruli within kidneys of rats from weaning to more than 12 months old (i.e., body weight ranging from 39 g to 643 g). For this purpose, the arterial injection of microspheres 7.5 μm to 17 μm in diameter was combined to corrosion-replication of the arterial bed of a vasodilated perfused kidney preparation. This procedure allowed easy detection of arterial by-passes with light microscope and detailed observation with scanning electron microscope. Our results clearly demonstrate the existence of various categories of arterial by-passes throughout renal cortex regardless of age. Some of them had never been described before. These vascular by-passes were found with increased frequency from superficial to juxtamedullary cortex. In the latter area, frequency was not agedependent, and approximately 10% (range 4-22%) of juxtamedullary glomeruli were involved. Data derived from previous microsphere studies would suggest that these structures are (partially) nonfunctioning in basal physiological conditions, but more information is needed to assess their possible functional role in the rat.
    Additional Material: 16 Ill.
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