Mataraza Jennifer M, Briggs Michael W, Li Zhigang, Entwistle Alan, Ridley Anne J, Sacks David B
Department of Pathology, Brigham and Women's Hospital and Harvard Medical School Boston, Massachusetts 02115, USA.
J Biol Chem. 2003 Oct 17;278(42):41237-45. doi: 10.1074/jbc.M304838200. Epub 2003 Aug 4.
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.
细胞迁移和侵袭的动态过程在很大程度上由Rho家族GTP酶协调。支架蛋白IQGAP1与Cdc42结合,在体外和细胞内均增加活性Cdc42的量。在此我们表明,IQGAP1在哺乳动物细胞中的过表达以依赖Cdc42和Rac1的方式增强细胞迁移。重要的是,使用小干扰RNA敲低内源性IQGAP1以及转染显性负性IQGAP1构建体IQGAP1DeltaGRD均显著降低细胞运动性。通过操纵细胞内IQGAP1浓度,细胞侵袭也同样发生改变。此外,IQGAP1DeltaGRD减弱了组成型活性Cdc42介导的侵袭。因此,IQGAP1在细胞运动性和侵袭中具有重要作用。