G protein-coupled receptor adaptation mechanisms

被引:153
作者
Ferguson, SSG
Caron, MG
机构
[1] John P Robarts Res Inst, London, ON N6A 5K8, Canada
[2] Univ Western Ontario, Dept Physiol, London, ON N6A 5K8, Canada
[3] Univ Western Ontario, Dept Pharmacol & Toxicol, London, ON N6A 5K8, Canada
[4] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
[5] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[6] Duke Univ, Med Ctr, Howard Hughes Med Inst, Durham, NC 27710 USA
关键词
arrestins; desensitization; G protein-coupled receptor kinases; sequestration; resensitization;
D O I
10.1006/scdb.1997.0216
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
G protein-coupled receptors (GPCRs) transduce extracellular signals that modulate the activity of a wide variety of biological processes, such as neurotransmission, chemoattraction, cardiac function, olfaction, and vision. However, GPCR signalling desensitizes rapidly as the consequence of receptor phosphorylation. G protein-coupled receptor kinase-mediated receptor phosphorylation promotes the binding of beta-arrestin proteins, which not only uncouple GPCRs from their cognate heterotrimeric G protein, but also target them for endocytosis. The sequestration (endocytosis) of desensitized GPCRs to endosomes is required for their dephosphorylation and subsequent resensitization to their pre-ligand exposed state. This review concentrates on the mechanisms underlying GPCR desensitization and resensitization. (C) 1998 Academic Press.
引用
收藏
页码:119 / 127
页数:9
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