Katoh Hironori, Hiramoto Kiyo, Negishi Manabu
Laboratory of Molecular Neurobiology, Graduate School of Biostudies, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.
J Cell Sci. 2006 Jan 1;119(Pt 1):56-65. doi: 10.1242/jcs.02720. Epub 2005 Dec 8.
Cell migration is essential for normal development and many pathological processes. Rho-family small GTPases play important roles in this event. In particular, Rac regulates lamellipodia formation at the leading edge during migration. The small GTPase RhoG activates Rac through its effector ELMO and the ELMO-binding protein Dock180, which functions as a Rac-specific guanine nucleotide exchange factor. Here we investigated the role of RhoG in cell migration. RNA interference-mediated knockdown of RhoG in HeLa cells reduced cell migration in Transwell and scratch-wound migration assays. In RhoG-knockdown cells, activation of Rac1 and formation of lamellipodia at the leading edge in response to wounding were attenuated. By contrast, expression of active RhoG promoted cell migration through ELMO and Dock180. However, the interaction of Dock180 with Crk was dispensable for the activation of Rac1 and promotion of cell migration by RhoG. Taken together, these results suggest that RhoG contributes to the regulation of Rac activity in migrating cells.
细胞迁移对于正常发育和许多病理过程至关重要。Rho家族小GTP酶在这一过程中发挥重要作用。特别是,Rac在迁移过程中调节前沿板状伪足的形成。小GTP酶RhoG通过其效应器ELMO和ELMO结合蛋白Dock180激活Rac,Dock180作为一种Rac特异性鸟嘌呤核苷酸交换因子发挥作用。在这里,我们研究了RhoG在细胞迁移中的作用。RNA干扰介导的HeLa细胞中RhoG的敲低在Transwell和划痕伤口迁移试验中降低了细胞迁移。在RhoG敲低的细胞中,Rac1的激活以及对伤口的反应中前沿板状伪足的形成减弱。相比之下,活性RhoG的表达通过ELMO和Dock180促进细胞迁移。然而,Dock180与Crk的相互作用对于Rac1的激活和RhoG促进细胞迁移是可有可无的。综上所述,这些结果表明RhoG有助于调节迁移细胞中Rac的活性。