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Rho GTP酶、磷酸肌醇和肌动蛋白:高效囊泡运输的三方框架。

Rho GTPases, phosphoinositides, and actin: a tripartite framework for efficient vesicular trafficking.

作者信息

Croisé Pauline, Estay-Ahumada Catherine, Gasman Stéphane, Ory Stéphane

机构信息

CNRS UPR 3212; Institut des Neurosciences Cellulaires et Intégratives; Université de Strasbourg; Strasbourg, France.

出版信息

Small GTPases. 2014;5:e29469. doi: 10.4161/sgtp.29469. Epub 2014 Jun 10.

Abstract

Rho GTPases are well known regulators of the actin cytoskeleton that act by binding and activating actin nucleators. They are therefore involved in many actin-based processes, including cell migration, cell polarity, and membrane trafficking. With the identification of phosphoinositide kinases and phosphatases as potential binding partners or effectors, Rho GTPases also appear to participate in the regulation of phosphoinositide metabolism. Since both actin dynamics and phosphoinositide turnover affect the efficiency and the fidelity of vesicle transport between cell compartments, Rho GTPases have emerged as critical players in membrane trafficking. Rho GTPase activity, actin remodeling, and phosphoinositide metabolism need to be coordinated in both space and time to ensure the progression of vesicles along membrane trafficking pathways. Although most molecular pathways are still unclear, in this review, we will highlight recent advances made in our understanding of how Rho-dependent signaling pathways organize actin dynamics and phosphoinositides and how phosphoinositides potentially provide negative feedback to Rho GTPases during endocytosis, exocytosis and membrane exchange between intracellular compartments.

摘要

Rho GTP酶是众所周知的肌动蛋白细胞骨架调节因子,通过结合并激活肌动蛋白成核剂发挥作用。因此,它们参与许多基于肌动蛋白的过程,包括细胞迁移、细胞极性和膜运输。随着磷酸肌醇激酶和磷酸酶被鉴定为潜在的结合伙伴或效应器,Rho GTP酶似乎也参与了磷酸肌醇代谢的调节。由于肌动蛋白动力学和磷酸肌醇周转都影响细胞区室之间囊泡运输的效率和保真度,Rho GTP酶已成为膜运输中的关键参与者。Rho GTP酶活性、肌动蛋白重塑和磷酸肌醇代谢需要在空间和时间上进行协调,以确保囊泡沿着膜运输途径前进。尽管大多数分子途径仍不清楚,但在本综述中,我们将重点介绍我们在理解Rho依赖性信号通路如何组织肌动蛋白动力学和磷酸肌醇,以及磷酸肌醇如何在内吞作用、外排作用和细胞内区室之间的膜交换过程中潜在地对Rho GTP酶提供负反馈方面取得的最新进展。

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本文引用的文献

1
Rho'ing in and out of cells: viral interactions with Rho GTPase signaling.
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2
Intersectin: The Crossroad between Vesicle Exocytosis and Endocytosis.
Front Endocrinol (Lausanne). 2013 Aug 27;4:109. doi: 10.3389/fendo.2013.00109. eCollection 2013.
4
Spatiotemporal control of endocytosis by phosphatidylinositol-3,4-bisphosphate.
Nature. 2013 Jul 11;499(7457):233-7. doi: 10.1038/nature12360. Epub 2013 Jul 3.
5
Plasma membrane tension orchestrates membrane trafficking, cytoskeletal remodeling, and biochemical signaling during phagocytosis.
Proc Natl Acad Sci U S A. 2013 Jul 16;110(29):11875-80. doi: 10.1073/pnas.1301766110. Epub 2013 Jul 2.
6
RAS and RHO families of GTPases directly regulate distinct phosphoinositide 3-kinase isoforms.
Cell. 2013 May 23;153(5):1050-63. doi: 10.1016/j.cell.2013.04.031.
7
Hijacking of Rho GTPases during bacterial infection.
Exp Cell Res. 2013 Sep 10;319(15):2329-36. doi: 10.1016/j.yexcr.2013.04.021. Epub 2013 May 3.
8
The signalling factor PI3K is a specific regulator of the clathrin-independent dynamin-dependent endocytosis of IL-2 receptors.
J Cell Sci. 2013 Mar 1;126(Pt 5):1099-108. doi: 10.1242/jcs.110932. Epub 2013 Jan 23.
10
Regulation of small GTPases by GEFs, GAPs, and GDIs.
Physiol Rev. 2013 Jan;93(1):269-309. doi: 10.1152/physrev.00003.2012.

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