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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 119 (1966), S. 425-433 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The nucleoli of cells of the adult mouse were examined by staining with toluidine blue after removal of deoxyribonucleic acid from tissue sections by deoxyribonuclease treatment.The nuclei of each cell type examined contained one or more nucleoli. This was observed even in lymphocytes and neuroglia, although these cells have occasionally been described as anucleolated. In mature spermatids and spermatozoa, however, it was not possible to detect a nucleolus.The distribution of the number of nucleoli in many diploid cells exhibited a mode of two or three nucleoli per nucleus, and a range from 1 to 6 nucleoli.In presumedly diploid hepatic nuclei, the maximum number of nucleoli was six; but in presumedly tetraploid hepatic nuclei, it was 11. Thus, nearly twice as many nucleoli are present when the chromosome number is doubled. In view of this observation, it is suggested that six nucleolar organizers are present in the diploid chromosomal complement of the mouse. However, through failure of some nucleolar organizers or more probably through fusion of nucleoli, the number of these organelles in most nuclei is less than six.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 153 (1965), S. 55-70 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The ameloblasts (and associated cells) of adult rat incisors were examined in sections stained with tannic acid-phosphomolybdic acid-amino black (TPA), a method which demonstrates the fibrillar structures of cytoplasm referred to as cell web, as well as terminal bars and desmosomes. These structures were analyzed at various stages of the life cycle of ameloblasts.The first sign of a cell web is found in the immature ameloblasts observed toward the end of the proliferation zone. Delicate vertical fibrils appear, which persist in various forms throughout the zones of differentiation, secretion, post-secretion, pigmentation and regression. These vertical fibrils are present along the lateral cell wall in most zones. In the post-secretion zone, a coarse fiber appears in the axis of the cell within the supranuclear region. This fiber splits at both ends into fine fibrils running toward the apex and base of the ameloblast, where delicate desmosomes are visible.A first set of terminal bars arises at the base of ameloblasts in the zone of proliferation. These “basal” terminal bars persist in all except the regression zone. A second set of terminal bars appears at the apex of the ameloblasts in the zone of differentiation. These “apical” terminal bars reach their maximal development in the secretion zone and disappear in the regression zone. Finally, desmosomes are prominent in the post-secretion and pigmentation zones, mainly on the apical and basal surfaces of the cells.The staining of terminal bars and desmosomes with TPA is presumably due to the accumulation of cell web fibrils on these attachment sites. The cell web may impart rigidity to the cell and provide resistance to stress wherever the fibrils are inserted on desmosomes and terminal bars.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 154 (1966), S. 41-71 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: To find out whether or not mammalian cells have a surface coat, over 50 cell types were examined in rat tissues stained with the periodic acid-Schiff technique for glycoproteins or the colloidal iron technique for acidic carbohydrates.With both techniques, nearly all cells investigated are outlined by a thin, but definite band of stained material, indicating the existence of a surface layer. The surface layer is uniform in leucocytes, fibrocytes and other cells of mesenchymal origin. This is true in neurons too, although associated structures may also be stained. In simple epithelia, the layer appears thicker at apical than at lateral and basal surfaces. (At the basal surface, the layer separates the cell from the basement membrane, which is itself colloidal iron negative and therefore is not part of the cell coat.) Finally, the layer is usually interrupted at the tight junction of terminal bars (where the cell interspace disappears as the plasma membranes of adjacent cells fuse). This finding confirms that the layer is not part of the plasma membrane itself but is a surface ‘cell coat.’In agreement with biochemical data, the staining properties indicate the presence of glycoprotein(s) and acidic residues in the coat of rat cells.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0003-276X
    Keywords: Feulgen reaction ; Cell cycle ; Chromosomes ; Interphase ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The Feulgen reaction has been utilized to localize DNA in nuclei throughout the cycle of mouse duodenal crypt cells using Epon-embedded 1 μm thick sections. The observed changes indicate that the 12.3 h long mitotic cycle of these cells can be subdivided into eleven stages, seven of which take place during the interphase. Computer measurements of Feulgen-stained nuclei and previous radioautographic studies indicate that DNA synthesis begins during stage I and ends during stage IV. The staining pattern shows no distinctive feature in the nuclei of the 1.5 h long stage I. Thereafter, marked changes occur during the rest of the interphase - that is during the 6.3 h that precede karyokinesis and the 3.5 h that follow it. Thus, at stage II the background of the nuclei darkens; at stage III, there appear stained threads interpreted as densifying chromosomes and dots interpreted as chromomeres, both of which thicken from 0.2 to 0.4 μm; at stage IV they further thicken to about 0.5 μm and at stage V, to about 0.7 μm. At this stage, which approximately corresponds to prophase, the intensely stained, discrete dots are localized within the less intensely stained sausage-shaped threads. As the breakup of the nuclear envelope introduces stage VI, whose early part corresponds to prometaphase, the intensely stained dots become close to one another within the threads and eventually fuse. The staining of the threads thus intensifies, and, by the late part of the stage that corresponds to metaphase, they have become the homogeneously dense metaphase chromosomes. At stage VII, the anaphase chromosomes reach each pole where they associate into a compact mass. This mass remains solid at stage VIII but gradually dissociates during stages IX, X, and XI as chromosomes are disassembled. © 1994 Wiley-Liss, Inc.
    Additional Material: 3 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 121 (1955), S. 1-12 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Additional Material: 11 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 170 (1971), S. 421-435 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The source of the new nuclei appearing during the growth of muscle fibers was examined in the tibialis anterior muscle of young Sherman rats (14-17 days of age) using radioautography at various intervals after a single injection of a small, non-toxic dose of 3H-thymidine (2 μCi/g body weight). Two techniques were employed: (1) labeled nuclei were detected in 1 μ thick radioautographs examined in the light microscope, and identified by simultaneous electron microscope examination of an adjacent section. The nuclei were then classified either as “true” muscle nuclei (within the plasmalemma of the fibers) or as belonging to “satellite cells” (which are mononucleated cells with scanty cytoplasm wedged between plasmalemma and basement membrane). (2) Muscle fibers freed by collagenase digestion were radioautographed one hour after 3H-thymidine injection in order to determine the total number of labeled nuclei (true muscle nuclei plus those of satellite cells) per unit length of fiber.Certain nuclei within the basement membrane of muscle fibers are labeled one hour after 3H-thymidine and, therefore, synthesize DNA. The electron microscope demonstrates that these nuclei invariably belong to satellite cells, never to true muscle nuclei. Furthermore, the total number of labeled nuclei per unit length of fiber doubles between 1 and 24 hours; and, therefore, the labeled satellite cell nuclei undergo mitosis.Following mitosis, half of the daughters of satellite cells are incorporated into the fibers to become true muscle nuclei. The remaining half divides again later; and half of their daughter cells are incorporated. Thus, satellite cells in young rats divide repeatedly and function as a source of true muscle nuclei.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 132 (1958), S. 247-259 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 165 (1969), S. 543-557 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Light and electron microscopic radioautographs of the tissues of young rats which were sacrificed at various times after a single 3H-ribose injection revealed a wide distribution of the label.Nuclear reactions were seen over hepatocytes and other cell types. After removal of RNA by treatment with RNAse, most nuclear reactions were absent; they were, therefore, attributed to the incorporation of label into newly-synthesized RNA. In about 2% of the nuclei, however, labeling persisted after RNAse, but was absent after DNAse treatment, indicating uptake into newly-synthesized DNA. Hence, ribose may be taken up into nucleic acidsundergoing synthesis.In cells of liver and cartilage as well as in some muscle fibers, moderate reaction appeared over glycogen areas. Removal of the label by salivary amylase confirmed its uptake into glycogen.In mucous and other secretory cells, amylase resistant radioautographic reactions appeared over the Golgi region and later over secretion products. Presumably the label was incorporated into the glycoproteinmoieties of these secretions.Many, if not all, cells in the body appear to be able to utilize free exogenous ribose. It is presumed that ribose is first phosphorylated and then either incorporated into the RNA and DNA being synthesized in the nucleus or converted into the glucose or fructose derivatives used for glycogen and glycoprotein synthesis in the cytoplasm. That these pathways may play a significant physiological role is suggested by the recent finding of free ribose in the blood.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 224 (1989), S. 123-138 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The production of type I collagen by fibroblasts, odontoblasts, and osteoblasts is reviewed on the basis of results obtained by electron microscopy, 3H-proline radioautography, and immunostaining for type I procollagen.In the three cell types, the percursors of type I collagen are processed along the rough endocplasmic reticulum (rER)-Golgic-secretory granule pathway in the same manner as secretory proteins, but the available evidence suggests a few special features: (1) From the rER site of synthesis, the initial collagen procursors, known as pro-alpha chains, are transported to the Golgi apparatus within tubular structures, referred to as intermediate tubules, rather than within vesicles. (2) The pro-alpha chains coil into a triple helix within spherical distensions present along the saccules on the cis side of Golgi stacks. (3) The resulting procollagens are fairly raigid and form bundles that cause spherical distensions to lengthen into cylindrical ones, whereas by an unknown mechanism these distensions become part of the saccules on the trans-side of Golgi stacks. (4) The procollagen-containing cylindrical distensions are resleased from trans-saccules to become secretory granules, and some procollagen material finds its way into lysosomes. (5) The secretory granules release their procollagen content by exocytosis at the cell surface. (6) The released procollagen is transformed into collagen before or, more probably, after associating with the surface of a collagen fibril.
    Additional Material: 38 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 86 (1950), S. 289-341 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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