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  • Microtubule organizing center  (2)
  • [abr] HD5; IV^3NeuGc-nLcOse"4Cer  (2)
  • 1
    ISSN: 0006-291X
    Keywords: [abr] GSL; glycosphingolipid ; [abr] HD3; II^3NeuGc-LacCer ; [abr] HD5; IV^3NeuGc-nLcOse"4Cer ; [abr] HD; Hanganutziu-Deicher ; [abr] NeuGc; N-glycolylneuraminicacid
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0006-291X
    Keywords: [abr] GSL; glycosphingolipid ; [abr] HD3; II^3NeuGc-LacCer ; [abr] HD5; IV^3NeuGc-nLcOse"4Cer ; [abr] HD; Hanganutziu-Deicher ; [abr] NeuGc; N-glycolylneuraminicacid
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 127 (1985), S. 133-146 
    ISSN: 1615-6102
    Keywords: Cytokinesis ; Dictyostelium ; Locomotion microtubule ; Motility ; Microtubule organizing center
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The microtubule inhibitors, ethyl-N-phenylcarbamate (EPC) and thiabendazole (TB), which disrupt cytoplasmic microtubules and induce giant cells inDictyostelium (Kitanishi et al. 1984), were found to induce the occurrence of multiple microtubule organizing centers (MTOCs) in these giant cells. Probing was done by indirect immunofluorescence using monoclonal anti-α-tubulin. The nuclear DNA content of the giant cells increased in parallel with an increase in the number of MTOCs, as shown by microspectrophotometory of cells stained with the fluorescent DNA stain DAPI (4′,6-diamidino-2-phenylindole). Shortly after the inhibitors were removed, the MTOCs of the giant cell formed multiple mitotic spindles or synchronously reconstituted numerous cytoplasmic MT-networks. These events apparently reflected the cell-cycle dependent activities of the MTOCs at the time the inhibitors were removed. When multiple spindles were formed, numerous cytoplasmic MT-networks became organized subsequent to the breakdown of the spindles. In either case, reconstitution of the cytoplasmic MT-networks was followed by apparently normal cytokinesis resulting in the production of many daughter cells each containing a single MT-MTOC complex. The evidence suggested the possible mechanism of the induction of multiple MTOCs, and implied that the MT-MTOC complex is significant in the cytokinesis ofDictyostelium by determining the cell locomotory unit.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 127 (1985), S. 212-221 
    ISSN: 1615-6102
    Keywords: Dictyostelium ; Microtubule(s) ; Microtubule organizing center ; Saltatory movement
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The microtubule organizing center (MTOC) was isolated fromDictyostelium discoideum to investigate the fine structure of the components as the first step in clarifying its molecular organization and function. The isolation protocol was designed to preserve microtubules bound to the MTOC by using indirect immunofluorescence employing anti-α-tubulin. After cell lysis with Triton X-100, the MTOCs were isolated in association with the nucleus by centrifugation in a microtubule-stabilizing buffer. The MTOC was found to be bound to the nucleus via an electron-dense fibrous structure, and this linkage could not be destroyed by KI, KCl, or sonication. We named this complex composed of microtubules, MTOC, and the anchor the MTOC-complex. Negative staining of the isolated MTOC-complex revealed that distinct vesicles decorated with 11-nm tacks were associated with microtubules radiating from the MTOC. Fine filaments, 4–5 nm wide, were also present close to the MTOC, aligned parallel to the microtubules. The three-dimensional profile of the central core of the MTOC, examined by transmission electron microscopy of serial thin sections of the isolated MTOC fraction supplemented by a microcomputer analysis, was concluded to be a matchbox-like cuboid (180 × 210 × 370 nm) of 15 layers. We propose that theDictyostelium MTOC is the structural domain of a more complicated unit composed of 1. MTOC, 2. microtubules, and 3. a firm fibrous linkage connecting the MTOC to the nucleus, with the MTOC core being a multilayered cuboid, associated with nodules and surrounded by amorphous electron-dense material including peculiar vesicles with 11 nm-tacks. The possible functions of these domains are discussed.
    Type of Medium: Electronic Resource
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