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  • 1985-1989
  • 1980-1984  (104)
  • 1915-1919
  • 1983  (104)
  • Ultrastructure  (104)
  • 101
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 228 (1983), S. 389-403 
    ISSN: 1432-0878
    Keywords: Lymph node, avian ; Ultrastructure ; Macrophages ; Phagocytic capacity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The structure of the avian lymph node (ALN) is characterized by a thin capsule, thin lymphoreticular cords, and an absence of trabeculae. It is not possible to subdivide the ALN into cortex, paracortex and medulla, or to subdivide the system of sinuses into marginal, trabecular and medullary divisions. The lymphoreticular cords contain avian germinal centers (AGC) with B-lymphocytes and the area of T-lymphocytes. Postcapillary venules are responsible for the recirculation of lymphocytes. Sinus reticular cells do not exist in the ALN, but free macrophages are present. The phagocytic capacity of the macrophages was determined by injection of vital dyes (India ink, Berlin blue) and inoculation with Candida cells. Macrophages filled with markers migrate from the lymph sinuses into the lymphoreticular cords and further into the AGC. The mobility of the macrophages is remarkably lower after phagocytosis of Candida cells.
    Type of Medium: Electronic Resource
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  • 102
    ISSN: 1432-0878
    Keywords: UV-irradiation ; Compound eye Rhabdomeres ; Trophospongium ; Ultrastructure ; Lepidoptera, Insecta
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Presumably, as a consequence of a 3-h exposure to light of 350-nm wavelength (1.5 × 1015 photons/cm2 sec) followed by a period of 20 h of rest in the dark, the four smaller retinula cells in each ommatidium of the eye of the butterfly Papilio xuthus contain a structure in the peripheral regions of their cytoplasm that resembles a portion of a rhabdom. Evidence for and against the view that this unusual, highly ordered arrangement of membranes represents a trophospongium is presented. In view of the fact that the structure in question only occurred at the same time when rhabdomeres were in a process of disintegration or reformation, the authors conclude that the structure in question is involved in the supply or removal of substances during a period of considerable activity of the retinula cell.
    Type of Medium: Electronic Resource
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  • 103
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 231 (1983), S. 143-155 
    ISSN: 1432-0878
    Keywords: Stellate cell ; Nongranulated cell ; Phagocyte ; Pars distalis ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary When the stellate cells (nongranulated cells) from dissociated-cell preparations of the anuran pars distalis were examined, they were seen to contain debris within phagocytic vacuoles (phagosomes). These phagosomes were variable; some contained granules from secretory cells while others were similar to lipid-like bodies and myelin figures. In situ partes distales from frogs were examined at the breeding season. The tissues were divided into lobules that were bounded by processes of stellate cells located between the secretory cells. Processes of stellate cells in the interior of a lobule interdigitate with processes extending inward from the stellate cells forming the border of the lobule. When these processes come together, a small cavity is formed. In many of the intact frogs the spaces between the stellate and secretory cells were greatly enlarged. At this particular time the processes of the stellate cells were attenuated and enclosed secretory granules that were also present as debris in these dilated, intercellular spaces. Within the cytoplasm of these stellate cells were not only phagosomes containing secretory granules but also organelles that appeared to be lipid bodies and lysosomes. Thus, the stellate cells of the pars distalis function in vivo, as well as in vitro, as phagocytes. In addition, macrophage-like cells moving from the blood may form another component of this system of phagocytes.
    Type of Medium: Electronic Resource
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  • 104
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 234 (1983), S. 679-689 
    ISSN: 1432-0878
    Keywords: Odontogenesis ; Rats ; Cyclophosphamide ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Cyclophosphamide-induced changes in rodent odontogenesis were investigated by light and electron microscopy in four-day-old Sprague Dawley rats given one injection of 40 mg/kg of body weight of cyclophosphamide and killed at intervals of one hour, one day, one week and two weeks. Incisor and molar teeth were dissected from the animals, fixed in 2.0% glutaraldehyde in 0.1 M sodium cacodylate with 3.4% sucrose, and subsequently some were incubated for alkaline phosphatase reaction, and embedded in Spurr's medium for sectioning at light- and electron-microscopic levels. From three days a cell-sparse zone was created in the pulp in the growing end of the tooth and progressive cellular changes were observed which became more severe in the one-week and two-week specimens. Subodontoblast and adjacent pulpal cells were the most affected showing nuclear changes, damage to, or loss of, organelles, and inclusion bodies. Odontogenic epithelium was less affected and odontoblasts appeared to be unaffected by the drug. A new irregular matrix was laid down in the defect area and seemed to be the product of depolarized odontoblasts. This new matrix showed alkaline phosphatase activity, as did the cells embedded in it, and later it became mineralized. It is speculated that the polarity of odontoblasts might be maintained by an intact subodontoblastic layer; when this is lost the odontoblasts become depolarized and capable of secreting matrix from both ends.
    Type of Medium: Electronic Resource
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