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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 154 (1977), S. 427-458 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Simultaneous cine and electromyographic records of freely feeding, unanesthetized golden hamsters show that their motion and muscular activity during mastication differ from those of albino rats (Weijs, '75). Rats show only propalinal motion while hamsters show lateral translation as well. The masticatory muscles of hamsters and rats are generally similar, but their molar dentitions differ. The interlocking molar cusps of hamsters restrict propalinal protrusion and retrusion when the molars are in occlusion; however, hamsters readily unlock occlusion by a twisting movement in the horizontal plane. Rats may perform propalinal movements even with the teeth in occlusion.In mastication the hamstery's jaw moves laterally as well as vertically and anteroposteriorly. Chewing orbits typically reverse after one to three orbits. Reversal begins at the start of the upstroke and involves a lateral shift in the opposite direction with the mouth closed.Electromyograms show that symmetric and asymmetric activities of closing protrusive and closing retrusive muscles produce a unilateral force couple on both sides. (This couple accompanies a midline closing stroke.) When the mouth is closed, unilateral activity of closing retrusors and closing protrusors also induces lateral translation. A bilateral force couple pits the retrusors of one side against the protrusors on the opposite side. Simultaneous with lateral excursion to the opposite side of midline and the action of these closing muscles, the anterior digastric and lateral pterygoid muscles of one side fire asymmetrically.The mandible moves downward coincidently with bilateral activity of the digastrics and lateral pterygoids. As the jaw opens further, activity differences of the lateral pterygoids accompany a shift of the mandible toward midline. At the end of the downstroke, all masticatory muscles studied are silent. The jaw returns to midline when the adductors fire asymmetrically at the start of closing.Trituration appears to coincide with an initial simple protrusion, which is subsequently accompanied by lateral translation. Different food types are reduced by distint chewing patterns with the differences clearest when the teeth are near occlusion. During gnawing the lateral pterygoids and digastrics fire longer, and the closing muscles fire less strongly. Chewing patterns in golden hamsters appear more generalized than those of rats; the differences may be directly associated with the ability of hamsters to store food in their cheek pouches.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 105 (1959), S. 241-291 
    ISSN: 0362-2525
    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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  • 3
    ISSN: 0730-2312
    Keywords: collagen gene regulation ; collagen gene expression ; glucocorticoid collagen gene regulation ; retinoid collagen gene regulation ; dexamethasone ; trans-retinoic acid ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Glucocorticoids decrease type I procollagen synthesis by decreasing the steady state levels of procollagen mRNAs and mRNA synthesis. The present studies were undertaken to determine the functional sequences of the proα2(1) collagen gene required for the glucocorticoid-mediated decrease of type I procollagen mRNA synthesis. Embryonic mouse fibroblasts were stably transfected with the pR40 DNA CAT construct containing the 5′ flanking region fragment from -2048 to +54 and the intronic fragment from +418 to +1524 of the mouse α2(I) collagen gene. Dexamethasone treatment of these pR40 transfected fibroblasts resulted in a significant decrease in CAT activity which agrees with the glucocorticoid-mediated decrease of the steady state levels of type I procollagen mRNAs. To determine the ppossible role of the first intron fragment in the dexamethasone-mediated decrease of CAT activity, pR36, a CAT plasmid containing the first intron fragment and the SV40 early promoter, was trasnfected into mouse fibroblasts and treated with dexamethasone. No significant decrease in CAT activity was observed. The dexamethasone-mediated response was then localized within the 5′ flanking region by preparing a series of constructs containing internal deletions and transfecting these plasmids into mouse fibroblasts. The regions -2048 to -981 and -506 to -351 were required for the dexamethasone response of gene activity. However, the DNA stretch from -981 to -506 was not. Analysis of the DNA sequences of these regions revelaed a singel GRE at -1023 to -1018 and a modified doublet at -873 to -856. The doublet GRE contains and A/T strand switch of the third base pair as compared to the single GRE and is not necessary for dexamethasone regulation of gene activity. All-trans-retionic acid increased CAT activity of the same pR40 CAT construct transfected in the mouse fibroblasts. DNA sequencing revealed a RARE and a modified RARE in the stretch of DNA from -981 to -506. Deletion of only the latter DNA region eliminated the elevation of CAT activity elicited by all-trans-retinoic acid. Our results indicate that the single GRE and the RARE are required for glucocorticoid and retinoic acid regulation of proα2(I) collagen gene activity, respectively.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 40 (1989), S. 353-359 
    ISSN: 0730-2312
    Keywords: platelet activating factor (PAF, PAF-acether) ; neutrophils ; Krebs II cells ; phospholipid asymmetry ; phospholipase A2 ; acetyltransferase ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The biosynthesis of platelet-activating factor (PAF-acether or 1-O-2-acetyl-sn-glycero-3-phosphocholine) through the remodeling pathway was investigated at the subcellular level in two different cell lines. In human neutrophils, plasma membrane was isolated not only from granules, but also from internal membranes related to endoplasmic reticulum. Interestingly, the latter exhibited enhanced acetyltransferase upon neutrophil stimulation with ionophore A23187. A similar study was undertaken on the tumor strain Krebs-II cells. The enzyme acetyltransferase was found to be located only on an endoplasmic reticulum subfraction, whereas most alkylacyl-GPC, the source of PAF-precursor alkyl-lyso-GPC, was located in the plasma membrane inner leaflet. The topographical separation of enzyme and precursor emphasizes the central role of the intracellular phospholipase A2 in providing lyso-PAF to the acetyltransferase to form PAF-acether.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 220 (1988), S. 328-334 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The ultrastructure of the nonsensory cells (dark cells, transitional cells, and undifferentiated cells) of the frog semicircular canal was studied by using transmission electron microscopy in an attempt to correlate the structure with the functions of these epithelial cells. All the nonsensory cells were linked by tight junctions and desmosomes; this suggested that there is little paracellular ionic transport from perilymph to endolymph. In the dark cell epithelium, the apicai intercellular spaces were dilated; in the basal part, numerous basolateral plasma membrane infoldings, containing mitochondria, delimited electron-lucent spaces. The undifferentiated cells and the transitional cells were devoid of any basal membrane infolding. Surrounding the semicircular canal, very flattened and interdigitated mesothelial cells constituted a thin multilayer tissue which limited the perilymphatic space. The morphological aspect of the dark cells suggests that they may play a role in the secretion and/or in the reabsorption of endolymph, which bathes the apical pole of these cells. The undifferentiated and transitional cells can play a role in the maintenance of the endolymphatic ionic composition because of their apical tight junctions and desmosomes.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 238 (1994), S. 263-276 
    ISSN: 0003-276X
    Keywords: Tongue ; Surface ; Musculature ; Iguanidae ; Reptile ; S.E.M. ; Histology ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The anatomy of the hyo-lingual apparatus in the iguanid lizard Oplurus cuvieri has been studied by light microscopy and scanning electron microscopy. Four areas were observed on the dorsal lingual epithelium of the lizard. Tongue tips are covered with a smooth epithelium. Closely packed flattened and cylindriform papillae cover the foretongue. The surface of the midtongue bears an unpapillose epithelium. Short conical papillae are arranged on the two lateral posterior bundles of the tongue. At high magnification, microvilli and microridges are widely distributed over the surface of the papillae. The epithelium of the papillae is composed of cells filled with secretory granules. Each surface plays successive roles during food ingestion, intra-buccal transport, and swallowing. The mucous interpapillary spaces would serve the adherence between the tongue and the food, the smooth epithelium of the midtongue should facilitate movements of the prey toward the pharynx, and conical papillae of the hindtongue present a rough surface which should act on the prey during the swallowing phase. The intrinsic morphology of the tongue is rather similar to that previously described for iguanids, but fibers of M. verticalis encircles ventrally the lingual process. These fibers could act in tongue protrusion as previously suggested for agamids. The morphology and function of the extrinsic tongue musculature and the hyoid musculature, analysed by electrical stimulations, are similar to the previous descriptions in iguanids and agamids either for feeding or displaying functions. © 1994 Wiley-Liss, Inc.
    Additional Material: 14 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 240 (1994), S. 423-433 
    ISSN: 0003-276X
    Keywords: Anguidae ; Buccal cavity ; Histology ; SEM ; Taste buds ; Tongue ; Vomeronasal organ ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background. The ability to detect chemical cues is highly developed in Scleroglossa, and particularly in anguid lizards. This ability was predicted because anguids possess a well-developed vomeronasal organ (VNO) (or Jacobson's organ) and rely largely on chemical cues in various behaviours as other active foragers. In this work, we have investigated the possible functional association between tongue flicking and the VNO in the lizard Anguis fragilis.Methods. The morphology of the tongue and the buccal cavity was investigated by light and scanning electron microscopy. The kinematics of tongue and jaw movements was studied by high speed cinematography.Results. The epithelial cells of the ventral aspect of the tongue tips show microstructures (microridges, microfacets, micropores) which are not present on other areas of the mouth. Beneath the tongue, the floor of the buccal cavity shows two concave-like elevations suggesting a structural analogy with the anterior processes described in snakes. The apex and the internal margin of these processes bear parallel oblique ridges. Taste buds occur anteriorly on the buccal floor and on the palate and are abundant on the internal side and on the edge on the anterior processes. The tongue showed three modes of tongue flicking: simple downward extension, single oscillation, and multiple oscillations. At each tongue flick, the ventral surface of the tips was observed contacting the substratum. Immediately after the tongue retraction, the buccal floor moved slightly upward. The observation of tongue flicking with the mouth open showed that the anterior processes moved upward when the tongue was retracted.Conclusions. These observations suggest the following: (1) during tongue flicking the ventral surface of the tongue tips invariably makes contact with the substratum; (2) the microstructures of the tongue tips and the ridges of the anterior processes might be helpful for collecting and receiving, respectively, chemicals during tongue flicking; (3) the anterior processes may be apposed on the roof of the mouth next to the ducts of VNOs when the buccal floor is fully elevated; (4) due to their localization, the taste buds could be equally stimulated by the molecules transferred during tongue flicking. © 1994 Wiley-Liss, Inc.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 242 (1995), S. 96-102 
    ISSN: 0003-276X
    Keywords: Rat embryo ; In vitro culture ; Development ; Epicardium ; Subepicardial mesenchyme ; Wheat germ agglutinin-gold ; Cell labelling ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Background: The role of the villi and vesicles of the epicardium primordium in the formation of the epicardium has been extensively studied over the last decades. With regard to the cellular contents of the villi and vesicles of the epicardium primordium, in quail the presence of mesenchymal cells in the villi recently has been described. In the present study, we have determined whether the villi and vesicles of the epicardium primordium in rat embryos contain mesenchymal cells that originate from the transverse septum and if so, whether these cells will become part of the subepicardium.Methods: Mesenchymal cells in the transverse septum of rat embryos were labelled by a method consisting of in vitro whole embryo culture and labelling of the ectoderm and its daughter cells, using wheat germ agglutinin-gold (WGA-Au) as a marker.Results: In concordance with our observations in the standard noncultured rat embryos, labelled cells were present in the transverse septum, extending from the umbilical ring, i.e., the transition of amniotic epithelium to ectoderm, up to the villi, in the villi and vesicles, and subepicardially.Conclusions: These observations suggest that the epicardium primordium contains mesenchymal cells derived from the transverse septum. These cells reach the subepicardium, using the villi and vesicles of the epicardium primordium as their vehicle. © 1995 Wiley-Liss, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0730-2312
    Keywords: basic helix-loop-helix ; interleukin-1 ; interleukin-3 ; granulocyte-macrophage colony-stimulating factor ; progenitor ; transcription factor ; c-kit ligand ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The basic helix-loop-helix (bHLH) transcription factors form heterodimers and control steps in cellular differentiation. We have studied four bHLH transcription factors, SCL, lyl-1, E12/E47, and Id-1, in individual lineage-defined progenitors and hematopoietic growth factor - dependent cell lines, evaluating mRNA expression and the effects of growth factors and cell cycle phase on this expression. Single lineage-defined progenitors selected from early murine colony starts and grown under permissive conditions were analyzed by RT-PCR. SCL and E12/E47 were expressed in the vast majority of tri-, bi-, and unilineage progenitors of erythroid, macrophage, megakaryocyte, and neutrophil lineages. Expression for E12/E47 was not seen in unilineage megakaryocyte and erythroid or bilineage neutrophil/mast cell progenitors. Lyl-1 showed a more restricted pattern of expression, although expression was seen in some bi- and unilineage progenitors. No expression was detected in erythroid, erythroid-megakaryocyte-macrophage, macrophage-neutrophil, macrophage, or megakaryocytic progenitors. Id-1, an inhibitory bHLH transcription factor, was also widely expressed in all bi- and unilineage progenitors; only the trilineage erythroid-megakaryocyte-macrophage progenitors failed to show expression. Expression of these factors within a progenitor class was generally heterogeneous, with some progenitors showing expression and some not. This was seen even when two sister cells from the same colony start were analyzed. Id-1, but not E12/E47, mRNA was increased in FDC-P1 and MO7E hematopoietic cell lines after exposure to IL-3 or GM-CSF, Id-1, E12, and lyl-1 showed marked variation at different points in cell cycle in isoleucine-synchronized FDC-P1 cells. These results suggest that SCL, lyl-1, E12/E47, and Id-1 are important in hematopoietic progenitor cell regulation, and that their expression in hematopoietic cells varies in response to cytokines and/or during transit through cell cycle. © 1996 Wiley-Liss, Inc.
    Additional Material: 5 Ill.
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  • 10
    ISSN: 0730-2312
    Keywords: CoA-independent transacylase ; phospholipase D ; subcellular localization ; neutrophils ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Subcellular localizations of CoA-independent transacylase and phospholipase D enzymes have been investigated in human neutrophils performing a two-step gradient system to separate plasma membranes from internal membranes and from the bulk of granules. The internal membranes were constituted by endoplasmic reticulum and by a subpopulation of specific and tertiary granules. The enzymes activities were assayed in vitro on gradient fractions using exogenous substrates. Following cell prelabelling with [3H]alkyllyso-GPC, we also analyzed the in situ localization of labelled products involving the action of both enzymes. The CoA-independent transacylase activity, together with the CoA-dependent transacylase and acyltransferase activities were only located in the internal membranes. Following 15 min cell labelling, part of the [3H]alkylacyl-GPC was recovered in plasma membranes indicating a rapid redistribution of the acylated compound. Very high contents in arachidonate containing [3H]alkylacyl-GPC were recovered both in plasma membranes and internal membranes. Phospholipase D activity being assayed in the presence of cytosol, GTPγS and gradient fractions, only the plasma membrane fractions from resting or stimulated cells allowed the enzyme to be active. The [3H]alkylacyl-GP and [3H]alkylacyl-GPethanol, phospholipase D breakdown products from [3H]alkylacyl-GPC, obtained after neutrophil prelabelling and activation by phorbol myristate acetate, were exclusively present in the plasma membranes. In contrast, the secondary generated [3H]alkylacylglycerols were equally distributed between plasma and internal membranes. No labelled product was recovered on azurophil granules. These data demonstrate that internal membranes are the site of action of the CoA-independent transacylase and plasma membranes are the site of action of the phospholipase D. This topographical separation between CoA-independent transacylase which generated substrate and phospholipase D which degraded it, suggested that subcellular localisation and traffic of substrates within the cell can be important to regulate the enzymes. © 1996 Wiley-Liss, Inc.
    Additional Material: 6 Ill.
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