Pathak Ritu, Dermardirossian Celine
Departments of Immunology and Microbial Science; The Scripps Research Institute; La Jolla, CA USA.
Small GTPases. 2013 Jul-Sep;4(3):174-9. doi: 10.4161/sgtp.24616. Epub 2013 May 6.
Vesicle trafficking is crucial for delivery of membrane compartments as well as signaling molecules to specific sites on the plasma membrane for regulation of diverse processes such as cell division, migration, polarity establishment and secretion. Rho GTPases are well-studied signaling molecules that regulate actin cytoskeleton in response to variety of extracellular stimuli. Increasing amounts of evidence suggest that Rho proteins play a critical role in vesicle trafficking in both the exocytic and endocytic pathways; however, the molecular mechanism underlying the process remains largely unclear. We recently defined a mechanism of action for RhoA in membrane trafficking pathways through regulation of the octameric complex exocyst in a manuscript published in Developmental Cell. We have shown that microtubule-associated RhoA-activating factor GEF-H1 is involved in endocytic and excocytic vesicle trafficking. GEF-H1 activates RhoA in response to RalA GTPase, which in turn regulates the localization and the assembly of exocyst components and exocytosis. Our work defines a mechanism for RhoA activation in response to RalA signaling and during vesicle trafficking. These results provide a framework for understanding how RhoA/GEF-H1 regulates the coordination of actin and microtubule cytoskeleton modulation and vesicle trafficking during migration and cell division.
囊泡运输对于将膜区室以及信号分子递送至质膜上的特定位点以调节多种过程(如细胞分裂、迁移、极性建立和分泌)至关重要。Rho GTPases是经过充分研究的信号分子,可响应多种细胞外刺激来调节肌动蛋白细胞骨架。越来越多的证据表明,Rho蛋白在胞吐和胞吞途径的囊泡运输中起着关键作用;然而,这一过程背后的分子机制仍 largely不清楚。我们最近在发表于《发育细胞》的一篇论文中,通过调节八聚体复合物外排体,定义了RhoA在膜运输途径中的一种作用机制。我们已经表明,微管相关的RhoA激活因子GEF-H1参与胞吞和胞吐囊泡运输。GEF-H1响应RalA GTPase激活RhoA,进而调节外排体组分的定位和组装以及胞吐作用。我们的工作定义了一种RhoA在响应RalA信号和囊泡运输过程中被激活的机制。这些结果为理解RhoA/GEF-H1如何在迁移和细胞分裂过程中调节肌动蛋白和微管细胞骨架调节与囊泡运输的协调提供了一个框架。