Brandt Dominique T, Marion Sabrina, Griffiths Gareth, Watanabe Takashi, Kaibuchi Kozo, Grosse Robert
Institute of Pharmacology, University of Heidelberg, Heidelberg, Germany.
J Cell Biol. 2007 Jul 16;178(2):193-200. doi: 10.1083/jcb.200612071. Epub 2007 Jul 9.
The Diaphanous-related formin Dia1 nucleates actin polymerization, thereby regulating cell shape and motility. Mechanisms that control the cellular location of Dia1 to spatially define actin polymerization are largely unknown. In this study, we identify the cytoskeletal scaffold protein IQGAP1 as a Dia1-binding protein that is necessary for its subcellular location. IQGAP1 interacts with Dia1 through a region within the Diaphanous inhibitory domain after the RhoA-mediated release of Dia1 autoinhibition. Both proteins colocalize at the front of migrating cells but also at the actin-rich phagocytic cup in macrophages. We show that IQGAP1 interaction with Dia1 is required for phagocytosis and phagocytic cup formation. Thus, we identify IQGAP1 as a novel component involved in the regulation of phagocytosis by mediating the localization of the actin filament nucleator Dia1.
与Diaphanous相关的成肌蛋白Dia1可促使肌动蛋白聚合,从而调节细胞形状和运动。控制Dia1在细胞内定位以在空间上确定肌动蛋白聚合的机制在很大程度上尚不清楚。在本研究中,我们确定细胞骨架支架蛋白IQGAP1是一种Dia1结合蛋白,对其亚细胞定位是必需的。在RhoA介导的Dia1自抑制解除后,IQGAP1通过Diaphanous抑制域内的一个区域与Dia1相互作用。这两种蛋白共定位于迁移细胞的前端以及巨噬细胞中富含肌动蛋白的吞噬杯。我们表明,IQGAP1与Dia1的相互作用对于吞噬作用和吞噬杯形成是必需的。因此,我们确定IQGAP1是通过介导肌动蛋白丝成核剂Dia1的定位而参与吞噬作用调节的一种新成分。