IQGAP1 promotes cell motility and invasion

被引:178
|
作者
Mataraza, JM
Briggs, MW
Li, ZG
Entwistle, A
Ridley, AJ
Sacks, DB
机构
[1] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Royal Free & Univ Coll Sch Med, Ludwig Inst Canc Res, London W1W 7BS, England
[4] UCL, Dept Biochem & Mol Biol, London WC1E 6BT, England
关键词
D O I
10.1074/jbc.M304838200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The dynamic processes of cell migration and invasion are largely coordinated by Rho family GTPases. The scaffolding protein IQGAP1 binds to Cdc42, increasing the amount of active Cdc42 both in vitro and in cells. Here we show that overexpression of IQGAP1 in mammalian cells enhances cell migration in a Cdc42- and Rac1-dependent manner. Importantly, cell motility was significantly decreased both by knock down of endogenous IQGAP1 using small interfering RNA and by transfection of a dominant negative IQGAP1 construct, IQGAP1DeltaGRD. Cell invasion was similarly altered by manipulating intracellular IQGAP1 concentrations. Moreover, invasion mediated by constitutively active Cdc42 was attenuated by IQGAP1DeltaGRD. Thus, IQGAP1 has a fundamental role in cell motility and invasion.
引用
收藏
页码:41237 / 41245
页数:9
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