Senoo Hiroshi, Iijima Miho
Department of Cell Biology; Johns Hopkins University School of Medicine; Baltimore, MD USA.
Commun Integr Biol. 2013 Nov 1;6(6):e27681. doi: 10.4161/cib.27681. Epub 2014 Jan 8.
Ras GTPases and phosphatidylinositol 3-kinases mediate intracellular signaling in directed cell migration. During chemotaxis, cells spatially control the activation of Ras/PI (3,4,5)-trisphosphate (PIP3) signaling and translate extracellular chemical gradients into intracellular signal cascades. This process is called directional sensing, and enables persistent cell migration with extraordinary sensitivity in shallow, unstable gradients of chemoattractants. In our recent study, we identified a Rho GTPase and its guanine nucleotide exchange factor (GEF) as molecular modulators that transmit signals from G protein-coupled receptors to Ras/PIP3 signaling pathways. The proteins spatially stabilize Ras activation and PIP3 production toward higher concentrations of chemoattractants. Unlike known roles of Rho GTPases and GEFs, the function of these proteins in directional sensing is independent of the actin cytoskeleton and cell morphology. Our findings provide novel mechanistic insight into the precision of directional cell migration.
Ras小G蛋白和磷脂酰肌醇3激酶介导细胞定向迁移中的细胞内信号传导。在趋化作用过程中,细胞在空间上控制Ras/磷脂酰肌醇-3,4,5-三磷酸(PIP3)信号的激活,并将细胞外化学梯度转化为细胞内信号级联反应。这个过程称为方向感知,它能使细胞在趋化因子的浅而不稳定的梯度中以极高的灵敏度进行持续的细胞迁移。在我们最近的研究中,我们鉴定出一种Rho小G蛋白及其鸟嘌呤核苷酸交换因子(GEF)作为分子调节剂,它们将信号从G蛋白偶联受体传递到Ras/PIP3信号通路。这些蛋白质在空间上稳定Ras激活和PIP3生成,使其朝向更高浓度的趋化因子。与Rho小G蛋白和GEF的已知作用不同,这些蛋白质在方向感知中的功能独立于肌动蛋白细胞骨架和细胞形态。我们的研究结果为细胞定向迁移的精确性提供了新的机制见解。