Suppr超能文献

在细胞分裂过程中,MgcRacGAP通过RhoA调节皮层活性。

MgcRacGAP regulates cortical activity through RhoA during cytokinesis.

作者信息

Lee Jae-Seon, Kamijo Keiju, Ohara Naoya, Kitamura Toshio, Miki Toru

机构信息

Molecular Tumor Biology Section, Basic Research Laboratory, National Cancer Institute, Bethesda, MD 20892-4255, USA.

出版信息

Exp Cell Res. 2004 Feb 15;293(2):275-82. doi: 10.1016/j.yexcr.2003.10.015.

Abstract

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 U2OS 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.

摘要

尽管Rho GTPases调节多种细胞活动,但其在细胞分裂中的作用仍不清楚。在此我们表明,Rho调节因子MgcRacGAP的一种GTPase激活蛋白(GAP)缺陷型突变体(R386A)的表达在U2OS细胞胞质分裂期间诱导异常的皮质活动。从后期开始到细胞分裂后期,在表达MgcRacGAP R386A的细胞中观察到多个大泡。当有丝分裂期的泡形成过多时,胞质分裂受到抑制,并产生带有微核的细胞。据报道,泡形成是由异常的皮质活动引起的。MgcRacGAP R386A诱导的异常皮质活动被RhoA的显性负性形式抑制,但不被Rac1或Cdc42抑制。此外,组成型活性RhoA的表达在胞质分裂期间也诱导剧烈的皮质活动。与凋亡性泡形成不同,MgcRacGAP R386A诱导的泡形成不被ROCK抑制剂Y-27632抑制,这表明MgcRacGAP通过一条新的信号通路在胞质分裂期间调节皮质活动。我们提出,MgcRacGAP通过RhoA调节皮质运动,在胞质分裂中起关键作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验