MgcRacGAP regulates cortical activity through RhoA during cytokinesis

被引:36
作者
Lee, JS
Kamijo, K
Ohara, N
Kitamura, T
Miki, T
机构
[1] NCI, Mol Tumor Biol Sect, Basic Res Lab, Bethesda, MD 20892 USA
[2] Univ Tokyo, Inst Med Sci, Div Hematopoiet Factors, Minato Ku, Tokyo 1088639, Japan
基金
美国国家卫生研究院;
关键词
MgcRacGAP; RhoA; cytokinesis; cortical activity;
D O I
10.1016/j.yexcr.2003.10.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although Rho GTPases regulate multiple cellular events, their role in cell division is still obscure. Here we show that expression of a GTPase-activating protein (GAP)-deficient mutant (R386A) of the Rho regulator MgcRacGAP induces abnormal cortical activity during cytokinesis in U20S cells. Multiple large blebs were observed in cells expressing MgcRacGAP R386A from the onset of anaphase to the late stage of cell division. When mitotic blebbing was excessive, cytokinesis was inhibited, and cells with micronuclei were generated. It has been reported that blebbing is caused by abnormal cortical activity. The MgcRacGAP R386A-induced abnormal cortical activity was inhibited by the dominant negative form of RhoA, but not Rac1 or Cdc42. Moreover, expression of constitutively active RhoA also induced drastic cortical activity during cytokinesis. Unlike apoptotic blebbing, MgcRacGAP R386A-induced blebbing was not inhibited by the ROCK inhibitor Y-27632, suggesting that MgcRacGAP regulates cortical activity during cytokinesis through a novel signaling pathway. We propose that MgcRacGAP plays a pivotal role in cytokinesis by regulating cortical movement through RhoA. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:275 / 282
页数:8
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