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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
    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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  • 5
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Additional Material: 58 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 117 (1965), S. 73-87 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The fate of the cells of the stratified squamous epithelium of the esophagus was investigated radioautographically in young adult rats at various time intervals after a single injection of thymidine-H3.Soon after injection, labeled cells appeared in the basal layer of the epithelium (stratum basale). During the following 12 hours, the labeled cells completed DNA synthesis and mitosis, and mostly remained in the basal layer. After 12 hours, however, the labeled cells arising from the mitoses were transferred to the spinous layer (stratum spinosum) at the rate of 1.2% per hour.The respective fates of the two daughter cells of a mitosis were then examined using two-dimensional maps showing the location of the labeled nuclei at 24 and 48 hours after injection. It was assumed that any two nuclei located side by side and overlaid by a similar number of grains are the two daughter cells of a mitosis. Such pairs of labeled daughter cells fell into three categories: (1) Basal pairs, composed of two basal cells; (2) Outgoing pairs, composed of two spinous (or granular) cells; and (3) Mixed pairs, composed of one basal and one spinous (or granular) cell. Since three possibilities were encountered at the two time intervals, the mitoses could not be differential (in which case the pairs of daughter cells would consist of a cell remaining in the basal layer and another migrating to the spinous layer, that is, all pairs would be “mixed”). Instead, the frequency of the three types of pairs was such as to indicate that the transfer of a basal cell to the spinous layer is a chance event which can affect any basal cell (except those undergoing DNA synthesis or mitosis). Accordingly, the transfer of either or both daughter cells of a mitosis would also be due to chance.The transfer of a cell out of the basal layer is a critical step in the life of the cell, since it precludes further division and appears to trigger differentiation.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 126 (1969), S. 507-525 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The origin and fate of Paneth cells were examined in duodenum, jejunum and ileum of adult female mice, using radioautography after administration of 3H-thymidine either in a single injection or in drinking water for four days or as a continuous infusion for up to ten days. The tissues were fixed by perfusion with 4% paraformaldehyde. One-micron thick, Eponembedded single or serial sections were stained with Regaud's hematoxylin, radioautographed, and counterstained with safranin O.Mitosis of Paneth cells is never observed, nor are these cells ever labeled one hour after 3H-thymidine. Hence, Paneth cells do not divide.However, a few days after single injection or prolonged administration of 3H-thymidine, labeled Paneth cells appear. The first labeled cells have tiny granules but, as the cells age, larger and larger granules are observed.Adjacent to Paneth cells are slender undifferentiated cells which show frequent mitoses and early labeling. The evidence points to some of these cells transforming into Paneth cells. Since occasionally Paneth cells degenerate, the newly-formed ones would provide replacement for those which die, thus insuring the steady state of the Paneth cell population. The renewal of this population is characterized by a turnover time of about three weeks.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 124 (1969), S. 281-305 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The epithelium of duodenum, jejunum and ileum was investigated in adult female mice given an injection of3 H-thymidine and sacrificed at times varying from one hour to 14 days later. The tissues were fixed by perfusion with paraformaldehyde and embedded in Epon. One micron thick sections were cut singly or serially, radioautographed and stained with iron hematoxylin and safranin O. In addition, reconstruction of a crypt was made from serial sections of jejunum.The reconstruction of a crypt shows the well known columnar, goblet, Paneth, and argentaffin cells. There are also little known cell types referred to as oligomucous and granulo-mucous and pale cells with or without mucus. Of these cells, the only numerous ones are the oligomucous cells, which are located in the lower half of the crypts and contain a few or even only one mucous globule. In the electron microscope, they display long cisterns of rough endoplasmic reticulum parallel to the lateral cell membrane and similar to those observed in goblet cells.In radioautographs of the crypts neither goblet cells, nor Paneth cells, nor argentaffin cells show mitosis or label one hour after3 H-thymidine injection. Granulo-mucous and pale cells are only rarely labeled. In contrast, columnar and oligomucous cells frequently take up label and undergo mitosis. By 12 hours after injection labeled goblet cells have appeared. Since at that time 3 H-thymidine has left the circulation, the label must have been acquired by transformation of labeled columnar or oligomucous cells. Furthermore, since transitional forms between oligomucous and goblet cells are common, it is concluded that oligomucous cells are those which directly transform into goblet cells.Eventually, like columnar cells, labeled goblet cells migrate to the villus epithelium, climb to the villus tip and fall into the lumen.Although oligomucous cells fit the requirements for goblet cell precursors, not enough of them are labeled to account for the rate of renewal of goblet cells. It is therefore speculated that some undifferentiated columnar cells at the base of the crypts participate in the production of oligomucous cells, which in turn yield goblet cells.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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