Literature DB >> 521456

Evidence for rapid structural and functional changes of the melanophore microtubule-organizing center upon pigment movements.

M Schliwa, U Euteneuer, W Herzog, K Weber.   

Abstract

Melanophores of the angelfish, pterophyllum scalare, have previously been shown to display approximately 2,400 microtubules in cells wih pigment dispersed; these microtubules radiate from a presumptive organizing center, the central apparatus (CA), and their number is reduced to approximately 1,000 in the state with aggregated pigment (M. Schliwa and U. Euteneuer, 1978, J. Supramol. Struct. 8:177-190). In an attempt to elucidate the factors controlling this rapid reorganization of the microtubule apparatus, structure and function of the CA have been investigated under different physiological conditions. As a function of the state of pigment distribution, melanophores differ markedly with respect to CA organization. A complex of dense amorphous aggregates and associated fuzzy material, several micrometers in diameter, surrounds the centrioles in cells with pigment dispersed, and numerous microtubules emanate from this complex in a radial fashion. In the aggregated state, on the other hand, few microtubules are observed in the pericentiolar region, and the amount of fibrous material is greatly reduced. These changes in CA morphology as a function of the state of pigment distribution are associated with a marked difference in its capacity to initiatiate the assembly of microtubules from exogenous pure porcine brain tubulin in lysed cell preparations. After complete removal of preexisting microtubules, cells lysed in the dispersed state into a solution of 1-2 mg/ml pure tubulin have numerous microtubules associated with the CA in radial fashion, while cells lysed in the aggregated state nucleate the assembly of only a few microtubules. We conclude that it is the activity of the CA that basically regulates the expression of microtubules. This regulation is achieved through a variation in the capacity to initiate microtubule assembly. Increase or decrease in the amount of dense material, as readily observed in the cell system studied here, seems to be a morphologic expression of such a physiologic function.

Entities:  

Mesh:

Substances:

Year:  1979        PMID: 521456      PMCID: PMC2110514          DOI: 10.1083/jcb.83.3.623

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


  19 in total

1.  In vitro assembly of pure tubulin into microtubules in the absence of microtubule-associated proteins and glycerol.

Authors:  W Herzog; K Weber
Journal:  Proc Natl Acad Sci U S A       Date:  1977-05       Impact factor: 11.205

2.  Microtubules in intracellular locomotion.

Authors:  K R Porter
Journal:  Ciba Found Symp       Date:  1973

3.  Microtubule assembly in the absence of added nucleotides.

Authors:  M L Shelanski; F Gaskin; C R Cantor
Journal:  Proc Natl Acad Sci U S A       Date:  1973-03       Impact factor: 11.205

4.  Fractionation of brain microtubule-associated proteins. Isolation of two different proteins which stimulate tubulin polymerization in vitro.

Authors:  W Herzog; K Weber
Journal:  Eur J Biochem       Date:  1978-12-01

5.  Microtubule system of isolated fish melanophores as revealed by immunofluorescence microscopy.

Authors:  M Schliwa; M Osborn; K Weber
Journal:  J Cell Biol       Date:  1978-01       Impact factor: 10.539

6.  In vitro polymerization of microtubules into asters and spindles in homogenates of surf clam eggs.

Authors:  R C Weisenberg; A C Rosenfeld
Journal:  J Cell Biol       Date:  1975-01       Impact factor: 10.539

7.  The role of spindle pole bodies and modified microtubule ends in the initiation of microtubule assembly in Saccharomyces cerevisiae.

Authors:  B Byers; K Shriver; L Goetsch
Journal:  J Cell Sci       Date:  1978-04       Impact factor: 5.285

8.  Iontophoretic release of cyclic AMP and dispersion of melanosomes within a single melanophore.

Authors:  I I Geschwind; J M Horowitz; G M Mikuckis; R D Dewey
Journal:  J Cell Biol       Date:  1977-09       Impact factor: 10.539

9.  The pericentriolar material in Chinese hamster ovary cells nucleates microtubule formation.

Authors:  R R Gould; G G Borisy
Journal:  J Cell Biol       Date:  1977-06       Impact factor: 10.539

10.  Nucleation of microtubules in vitro by isolated spindle pole bodies of the yeast Saccharomyces cerevisiae.

Authors:  J S Hyams; G G Borisy
Journal:  J Cell Biol       Date:  1978-08       Impact factor: 10.539

View more
  9 in total

1.  The microtubular system of crayfish retinula cells and its changes in relation to screening-pigment migration.

Authors:  E Frixione
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

Review 2.  Tension management in the kinetochore.

Authors:  Kerry Bloom; Elaine Yeh
Journal:  Curr Biol       Date:  2010-12-07       Impact factor: 10.834

3.  Mitotic spindle form and function.

Authors:  Mark Winey; Kerry Bloom
Journal:  Genetics       Date:  2012-04       Impact factor: 4.562

Review 4.  Cytomatrix in chromatophores.

Authors:  M E Stearns
Journal:  J Cell Biol       Date:  1984-07       Impact factor: 10.539

5.  Spatial organization of microtubule-organizing centers and microtubules.

Authors:  J B Tucker
Journal:  J Cell Biol       Date:  1984-07       Impact factor: 10.539

6.  Chromatophores--models for studying cytomatrix translocations.

Authors:  M A McNiven; K R Porter
Journal:  J Cell Biol       Date:  1984-07       Impact factor: 10.539

7.  A functional in vitro model for studies of intracellular motility in digitonin-permeabilized erythrophores.

Authors:  M E Stearns; R L Ochs
Journal:  J Cell Biol       Date:  1982-09       Impact factor: 10.539

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

Authors:  I Nemhauser; J Joseph-Silverstein; W D Cohen
Journal:  J Cell Biol       Date:  1983-04       Impact factor: 10.539

9.  Intracellular cyclic AMP not calcium, determines the direction of vesicle movement in melanophores: direct measurement by fluorescence ratio imaging.

Authors:  P J Sammak; S R Adams; A T Harootunian; M Schliwa; R Y Tsien
Journal:  J Cell Biol       Date:  1992-04       Impact factor: 10.539

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.