Literature DB >> 8505360

Mitotic block in HeLa cells by vinblastine: ultrastructural changes in kinetochore-microtubule attachment and in centrosomes.

K L Wendell1, L Wilson, M A Jordan.   

Abstract

Previous work from this laboratory has indicated that very low concentrations of vinblastine block HeLa cells at mitosis in the presence of a full complement of microtubules and without major disruption of spindle organization. In the present study we analyzed the structural organization of mitotic spindle microtubules, chromosomes and centrosomes by electron microscopy after incubating HeLa cells for one cell cycle with 2 nM vinblastine. We found that mitotic block of HeLa cells by vinblastine was associated with alterations of the fine structure of the spindle that were subtle but profound in their apparent consequences. The cell cycle was blocked in a stage that resembled prometaphase or metaphase; chromosomes had not undergone anaphase segregation. Neither the structure of the microtubules nor the structure of the kinetochores was detectably altered by the drug. However, the number of microtubules attached to kinetochores was decreased significantly. In addition, the centrosomes were altered; the normal close association of mother and daughter centriole was lost, numerous membranous vesicles were found in the centrosomal region, and many centrioles exhibited abnormal ultrastructure and had microtubules coursing through their interiors. These findings are consistent with our previous results and indicate that inhibition of the polymerization dynamics of mitotic spindle microtubules and perhaps of centriole microtubules, rather than microtubule depolymerization, is responsible for the mitotic inhibition by vinblastine.

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Year:  1993        PMID: 8505360     DOI: 10.1242/jcs.104.2.261

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  50 in total

1.  CENP-E is essential for reliable bioriented spindle attachment, but chromosome alignment can be achieved via redundant mechanisms in mammalian cells.

Authors:  B F McEwen; G K Chan; B Zubrowski; M S Savoian; M T Sauer; T J Yen
Journal:  Mol Biol Cell       Date:  2001-09       Impact factor: 4.138

2.  A common mechanism for mitotic inactivation of C2H2 zinc finger DNA-binding domains.

Authors:  Sinisa Dovat; Tapani Ronni; Dana Russell; Roger Ferrini; Bradley S Cobb; Stephen T Smale
Journal:  Genes Dev       Date:  2002-12-01       Impact factor: 11.361

3.  Mammalian mad2 and bub1/bubR1 recognize distinct spindle-attachment and kinetochore-tension checkpoints.

Authors:  D A Skoufias; P R Andreassen; F B Lacroix; L Wilson; R L Margolis
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-27       Impact factor: 11.205

4.  Nanomolar concentrations of nocodazole alter microtubule dynamic instability in vivo and in vitro.

Authors:  R J Vasquez; B Howell; A M Yvon; P Wadsworth; L Cassimeris
Journal:  Mol Biol Cell       Date:  1997-06       Impact factor: 4.138

5.  Relevance of kinetochore size and microtubule-binding capacity for stable chromosome attachment during mitosis in PtK1 cells.

Authors:  B F McEwen; Y Ding; A B Heagle
Journal:  Chromosome Res       Date:  1998-02       Impact factor: 5.239

Review 6.  The kinetochore-microtubule interface at a glance.

Authors:  Julie K Monda; Iain M Cheeseman
Journal:  J Cell Sci       Date:  2018-08-16       Impact factor: 5.285

7.  Phospholipase C is involved in kinetochore function in Saccharomyces cerevisiae.

Authors:  H Lin; J H Choi; J Hasek; N DeLillo; W Lou; A Vancura
Journal:  Mol Cell Biol       Date:  2000-05       Impact factor: 4.272

8.  Kinetochore fiber maturation in PtK1 cells and its implications for the mechanisms of chromosome congression and anaphase onset.

Authors:  B F McEwen; A B Heagle; G O Cassels; K F Buttle; C L Rieder
Journal:  J Cell Biol       Date:  1997-06-30       Impact factor: 10.539

9.  Mechanism of mitotic block and inhibition of cell proliferation by taxol at low concentrations.

Authors:  M A Jordan; R J Toso; D Thrower; L Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

10.  Checkpoint genes required to delay cell division in response to nocodazole respond to impaired kinetochore function in the yeast Saccharomyces cerevisiae.

Authors:  Y Wang; D J Burke
Journal:  Mol Cell Biol       Date:  1995-12       Impact factor: 4.272

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