CNRS UPR 3212, Institut des Neurosciences Cellulaires et Intégratives, Université de Strasbourg, Strasbourg, France.
Semin Cell Dev Biol. 2011 Feb;22(1):27-32. doi: 10.1016/j.semcdb.2010.12.002. Epub 2010 Dec 8.
Delivery of proteins or lipids to the plasma membrane or into the extracellular space occurs through exocytosis, a process that requires tethering, docking, priming and fusion of vesicles, as well as F-actin rearrangements in response to specific extracellular cues. GTPases of the Rho family have been implicated as important regulators of exocytosis, but how Rho proteins control this process is an open question. In this review, we focus on molecular connections that drive Rho-dependent exocytosis in polarized and regulated exocytosis. Specifically, we present data showing that Rho proteins interaction with the exocyst complex and IQGAP mediates polarized exocytosis, whereas interaction with actin-binding proteins like N-WASP mediates regulated exocytosis.
蛋白质或脂质被递送到质膜或细胞外空间是通过胞吐作用完成的,这个过程需要囊泡的锚定、对接、预备和融合,以及对特定细胞外信号的 F-肌动蛋白重排。Rho 家族的 GTPases 被认为是胞吐作用的重要调节剂,但 Rho 蛋白如何控制这个过程是一个悬而未决的问题。在这篇综述中,我们重点介绍了驱动极化和调节性胞吐作用中 Rho 依赖性胞吐作用的分子连接。具体来说,我们提出的数据表明,Rho 蛋白与胞外体复合物的相互作用和 IQGAP 介导极化胞吐作用,而与肌动蛋白结合蛋白如 N-WASP 的相互作用则介导调节性胞吐作用。