Division of Membrane Biology, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan Department of Cellular Regulation, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Osaka 565-0871, Japan Laboratory of Lipid Biochemistry, Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan.
Mol Biol Cell. 2013 Nov;24(21):3393-405. doi: 10.1091/mbc.E13-04-0178. Epub 2013 Sep 4.
The distinct levels of Rac activity differentially regulate the pattern of intrinsic cell migration. However, it remains unknown how Rac activity is modulated and how the level of Rac activity controls cell migratory behavior. Here we show that Slit-Robo GAP 1 (srGAP1) is a modulator of Rac activity in locomotive cells. srGAP1 possesses a GAP activity specific to Rac1 and is recruited to lamellipodia in a Rac1-dependent manner. srGAP1 limits Rac1 activity and allows concomitant activation of Rac1 and RhoA, which are mutually inhibitory. When both GTPases are activated, the protrusive structures caused by Rac1-dependent actin reorganization are spatially restricted and periodically destabilized, causing ruffling by RhoA-induced actomyosin contractility. Depletion of srGAP1 overactivates Rac1 and inactivates RhoA, resulting in continuous spatiotemporal spreading of lamellipodia and a modal shift of intrinsic cell motility from random to directionally persistent. Thus srGAP1 is a key determinant of lamellipodial dynamics and cell migratory behavior.
Rac 活性的不同水平差异调节内在细胞迁移的模式。然而,Rac 活性如何被调节以及 Rac 活性水平如何控制细胞迁移行为仍然未知。在这里,我们表明 Slit-Robo GAP1(srGAP1)是运动细胞中 Rac 活性的调节剂。srGAP1 具有 Rac1 特异性的 GAP 活性,并以 Rac1 依赖性方式募集到片状伪足。srGAP1 限制 Rac1 活性并允许 Rac1 和 RhoA 的同时激活,它们是相互抑制的。当两种 GTPase 都被激活时,由 Rac1 依赖性肌动蛋白重排引起的突起结构在空间上受到限制,并周期性地失稳,导致 RhoA 诱导的肌动球蛋白收缩引起的皱襞。srGAP1 的耗竭会过度激活 Rac1 并失活 RhoA,导致片状伪足的连续时空扩展,并导致内在细胞运动从随机到定向持续的模式转变。因此,srGAP1 是片状伪足动力学和细胞迁移行为的关键决定因素。