Literature DB >> 6833398

Centrioles as microtubule-organizing centers for marginal bands of molluscan erythrocytes.

I Nemhauser, J Joseph-Silverstein, W D Cohen.   

Abstract

The erythrocytes of blood clams (arcidae) are flattened, elliptical, and nucleated. They contain elliptical marginal bands (MBs) of microtubules, each physically associated with a pair of centrioles marginal bands (MBs) of microtubles, each physically associated with a pair of centrioles (Cohen, W., and I. Nemhauser, 1980, J. Cell Biol., 86:286-291). The MBs were found to be cold labile in living cells, disappearing within 1-2 h at 0 degrees C. After the cells had been rewarmed for 1-2 h, continuous MBs with associated centrioles were once again present. Time-course studies utilizing phase contrast, antitubulin immunofluorescence, and electron microscopy of cytoskeletons prepared during rewarming revealed structural evidence of centriole participation in MB reassembly. At the earliest stage of reassembly, a continuous MB was not present. Instead, relatively short and straight microtubules focused on a pointed centriolar "pole," and none were present elsewhere in the cytoskeleton. Thin continuous MBs then formed, still pointed in the centriolar region. Subsequently, the MBs regained ellipticity, with their thickness gradually increasing but not reaching that of controls even after several hours of rewarming. At these later time points, microtubules still radiated from the centrioles and joined the MBs some distance away. In the presence of 0.1 mM colchicines, MB reassembly was arrested at the pointed stage. Electron microscopic observations indicate that pericentriolar material is involved in microtubule nucleation in this system, rather than the centriolar triplets directly. The results suggest a model in which the centrioles and associated material nucleate assembly and growth of microtubules in diverging directions around the cell periphery. Microtubules of opposite polarity would then pass each other at the end of the cell distal to the centrioles, with continued elongation eventually closing the MB ellipse behind the centriole pair.

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Year:  1983        PMID: 6833398      PMCID: PMC2112335          DOI: 10.1083/jcb.96.4.979

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  29 in total

1.  Avian erythrocyte development: microtubules and the formation of the disk shape.

Authors:  L A Barrett; R B Dawson
Journal:  Dev Biol       Date:  1974-01       Impact factor: 3.582

2.  The microtubule marginal band of mammalian red blood cells.

Authors:  B van Deurs; O Behnke
Journal:  Z Anat Entwicklungsgesch       Date:  1973-12-31

3.  A comparative study of microtubules of disk-shaped blood cells.

Authors:  O Behnke
Journal:  J Ultrastruct Res       Date:  1970-04

4.  Fine structure of the hemocytes of Periplaneta americana (Orthoptera: Blattidae) with particular reference to marginal bundles.

Authors:  R J Baerwald; G M Boush
Journal:  J Ultrastruct Res       Date:  1970-04

5.  DNA metabolism and development of organelles in guinea-pig megakaryocytes: a combined ultrastructural, autoradiographic and cytophotometric study.

Authors:  J M Paulus
Journal:  Blood       Date:  1970-03       Impact factor: 22.113

Review 6.  Microtubules in disk-shaped blood cells.

Authors:  O Behnke
Journal:  Int Rev Exp Pathol       Date:  1970

7.  An electron microscope study of the rat megacaryocyte. II. Some aspects of platelet release and microtubules.

Authors:  O Behnke
Journal:  J Ultrastruct Res       Date:  1969-01

8.  Further studies on microtubules. A marginal bundle in human and rat thrombocytes.

Authors:  O Behnke
Journal:  J Ultrastruct Res       Date:  1965-12

9.  Nucleated sites for the assembly of cytoplasmic microtubules in the ectodermal cells of blastulae of Arbacia punctulata.

Authors:  L G Tilney; J Goddard
Journal:  J Cell Biol       Date:  1970-09       Impact factor: 10.539

10.  Incomplete microtubules observed in mammalian blood platelets during microtubule polymerization.

Authors:  O Behnke
Journal:  J Cell Biol       Date:  1967-08       Impact factor: 10.539

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  7 in total

1.  A planar microtubule-organizing zone in guard cells of Allium: experimental depolymerization and reassembly of microtubules.

Authors:  J Marc; Y Mineyuki; B A Palevitz
Journal:  Planta       Date:  1989-11       Impact factor: 4.116

2.  Specific protein phosphorylation occurs in molluscan red blood cell ghosts in response to hypoosmotic stress.

Authors:  A D Politis; S K Pierce
Journal:  J Membr Biol       Date:  1991-11       Impact factor: 1.843

3.  Re-formation of microtubules in Closterium ehrenbergii Meneghini after cold-induced depolymerization.

Authors:  T Hogetsu
Journal:  Planta       Date:  1986-04       Impact factor: 4.116

4.  Kinetics and intermediates of marginal band reformation: evidence for peripheral determinants of microtubule organization.

Authors:  M Miller; F Solomon
Journal:  J Cell Biol       Date:  1984-07       Impact factor: 10.539

5.  The cytoskeletal system of nucleated erythrocytes. III. Marginal band function in mature cells.

Authors:  J Joseph-Silverstein; W D Cohen
Journal:  J Cell Biol       Date:  1984-06       Impact factor: 10.539

6.  Development of a differentiated microtubule structure: formation of the chicken erythrocyte marginal band in vivo.

Authors:  S Kim; M Magendantz; W Katz; F Solomon
Journal:  J Cell Biol       Date:  1987-01       Impact factor: 10.539

7.  Immunofluorescence examination of beta tubulin expression and marginal band formation in developing chicken erythroblasts.

Authors:  D B Murphy; W A Grasser; K T Wallis
Journal:  J Cell Biol       Date:  1986-02       Impact factor: 10.539

  7 in total

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