G protein-coupled receptors stimulation and the control of cell migration

被引:143
作者
Cotton, Mathieu [1 ]
Claing, Audrey [1 ]
机构
[1] Univ Montreal, Fac Med, Dept Pharmacol, Montreal, PQ H3C 3J7, Canada
基金
加拿大健康研究院;
关键词
G protein-coupled receptors; Migration; Actin remodeling; G proteins; Arrestin; EPIDERMAL-GROWTH-FACTOR; VASCULAR SMOOTH-MUSCLE; BREAST-CANCER CELLS; LYSOPHOSPHATIDIC ACID RECEPTOR; EGFR SIGNAL TRANSACTIVATION; RHO-FAMILY GTPASES; HUMAN GLIOMA-CELLS; ADP-RIBOSYLATION; ANGIOTENSIN-II; NEURITE RETRACTION;
D O I
10.1016/j.cellsig.2009.02.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell migration is a fundamental biological process involved in normal physiology. Altered motile phenotypes are however often associated with the development and progression of diseases such as cancer and atherosclerosis. Remodeling of the actin cytoskeleton is required for cell shape changes and is controlled by a broad variety of cellular proteins. Interestingly, several extracellular stimuli can promote actin reorganization and result in enhanced cell migration. Namely, G protein-coupled receptors (GPCRs), which are activated by factors ranging from small amines, to hormones, and chemokines, initiate signalling cascades resulting in cell shape changes, formation of a migrating front (leading edge) and altered adhesion. GPCRs; are heptahelical membrane proteins, which classically transmit signal via the activation of heterotrimeric G proteins. Sustained stimulation leads to the activation of G protein-coupled receptor kinases (GRKs) and the recruitment of arrestin proteins, which engage alternative signalling pathways. In this review, we will discuss the role of GPCR mediated signal transduction and review their importance in the regulation of actin remodeling leading to cell migration. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1045 / 1053
页数:9
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