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  • 1
    ISSN: 1573-6822
    Keywords: astrocytes ; cytoskeleton ; embryonal carcinoma ; immunofluorescence ; methylmercury ; microtubules ; neurons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Immunofluorescence staining with antibodies to tubulin, neurofilaments and glial filaments was used to study the effects of methylmercury on the differentiation of retinoic acid-induced embryonal carcinoma cells into neurons and astroglia and on the cytoskeleton of these neuroectodermal derivatives. Methylmercury did not prevent undifferentiated embryonal carcinoma cells from developing into neurons and glia. Treatment of committed embryonal carcinoma cells with methylmercury doses exceeding 1 μM resulted in the formation of neurons with abnormal morphologies. In differentiated cultures, microtubules were the first cytoskeletal element to be affected. Their disassembly was time- and concentration-dependent. Microtubules in glial cells and in neuronal perikarya were more sensitive than those in neuronal processes. Neurofilaments and glial filaments appeared relatively insensitive to methylmercury treatment but showed reorganization after complete disassembly of the microtubules. The data demonstrate 1) the sensitivity of microtubules of both neurons and glia to methylmercury-induced depolymerization, and 2) the heterogeneous response of neuronal
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 6 (1986), S. 122-127 
    ISSN: 0886-1544
    Keywords: microtubules ; rootlets ; monoclonals ; immunofluorescence ; mitosis ; cytokinesis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We have used immunofluorescence staining with monoclonal antibodies to tubulin and to components of the flagellar basal apparatus to examine duplication of the basal apparatus and the microtubule system assembled from it during cell division in the quadriflagellate alga Polytomella. The monoclonal antitubulin, prepared against Polytomella flagellar axonemes, detects Polytomella and mammalian tubulin by immunoblotting. By immunofluorescence and immunogold electron microscopy, it detects all microtubular structures that have been described in Polytomella. One of the antibodies generated using the isolated basal apparatus as immunogen appears to stain four of the eight basal body rootlets and is used in this study to detect early stages in the duplication of the flagellar apparatus. A cytoplasmic microtubule system is present, the elongate morphology of the cell is maintained, and the cells are motile throughout mitosis. The closed mitotic spindle forms perpendicular to the long axis of the cell. During mitosis, the newly formed basal bodies mature and four additional elongating flagella appear. Following mitosis, the eight flagella segregate into two groups, which begin to separate towards opposite poles of the cell. Concomitant with this separation, the rootlets of the parental basal apparatus separate and new rootlets are detected. We suggest that the components of the parental flagellar apparatus are segregated equally to the daughter cells. An interphase cytoskeletal microtubule array is assembled from each basal apparatus, and the morphology of the two cells is progressively established during cytokinesis.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 24 (1993), S. 129-138 
    ISSN: 0886-1544
    Keywords: microtubules ; MTOC ; centrosome ; pericentriolar material ; cytolytic activity ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Immunofluorescence staining, electron microscopy, and (51Cr) cytolytic release assays are used to investigate the effects of taxol and taxol/hyperthermia treatments on the microtubule organization and cytolytic activity of cytotoxic T lymphocytes (CTLs). A 4 h treatment of CTLs with 1 μM taxol results in an extensive reorganization of the microtubule system to form one to a few large microtubule bundles that extend from the centrosome. The Golgi apparatus is not disrupted by this treatment and remains associated with the microtubule organizing centre (MTOC). This microtubule reorganization has no effect on the ability of CTLs to orient their MTOC towards a bound target cell, nor on their cytolytic activity. In control CTLs, not treated with taxol, a mild hyperthermia treatment (42°C, 30 min) results in an aggregation of the pericentriolar material, a loss of MTOC orientation, an inhibition of cytolytic activity, and a disorganization of the microtubule system [Knox et al.: Exp. Cell Res. 194:275-283, 1991]. In contrast, in taxol-treated CTLs the stabilized microtubule bundles are unaffected by such hyperthermia treatment; however, the other effects of hyperthermia appear identical in control and taxol-treated CTLs. These results indicate that a dynamic, radially arranged microtubule array is not required for the functional polarization of CTLs and suggest that a component of the pericentriolar material may play a key role in effecting MTOC orientation. © 1993 Wiley-Liss, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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