Vav GEFs regulate macrophage morphology and adhesion-induced Rac and Rho activation

被引:34
|
作者
Bhavsar, Parag J. [1 ,2 ]
Vigorito, Elena [3 ]
Turner, Martin [3 ]
Ridley, Anne J. [1 ]
机构
[1] Kings Coll London, Randall Div Cell & Mol Biophys, London SE1 1UL, England
[2] UCL, Dept Struct & Mol Biol, London WC1E 6BT, England
[3] Babraham Inst, Lab Lymphocyte Signalling & Dev, Cambridge, England
基金
英国生物技术与生命科学研究理事会;
关键词
NUCLEOTIDE EXCHANGE FACTORS; TYROSINE PHOSPHORYLATION; CELL-MIGRATION; SIGNAL-TRANSDUCTION; FAMILY PROTEINS; T-CELLS; GTPASES; REQUIREMENT; PAXILLIN; MOTILITY;
D O I
10.1016/j.yexcr.2009.08.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Vav family of proteins have the potential to act as both signalling adapters and GEFs for Rho GTPases. They have therefore been proposed as regulators of the cytoskeleton in various cell types. We have used macrophages from mice deficient in all three Vav isoforms to determine how their function affects cell morphology and migration. Macrophages lacking Vav proteins adopt ail elongated morphology and have enhanced migratory persistence in culture. To investigate the pathways through which Vav proteins exert their effects we analysed the responses of macrophages to the chemoattractant CSF-1 and to adhesion. We found that morphological and signalling responses of macrophages to CSF-1 did not require Vav Proteins. In contrast, adhesion-induced cell spreading, RhoA and Rac1 activation and cell signalling were all dependent oil Vav proteins. We Propose that Vav Proteins affect macrophage Morphology and motile behaviour by coupling adhesion receptors to Rac1 and RhoA activity and regulating adhesion signalling events such as paxillin and ERK1/2 phosphorylation by acting as adapters. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:3345 / 3358
页数:14
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