Endocytosis of G protein-coupled receptors:: roles of G protein-coupled receptor kinases and β-arrestin proteins

被引:428
作者
Claing, A
Laporte, SA
Caron, MG
Lefkowitz, RJ
机构
[1] Duke Univ, Med Ctr, Howard Hughes Med Inst, Dept Med Cardiol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Howard Hughes Med Inst, Dept Biochem, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Howard Hughes Med Inst, Dept Cell Biol, Durham, NC 27710 USA
基金
加拿大健康研究院;
关键词
D O I
10.1016/S0301-0082(01)00023-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sequestration of G protein-coupled receptors from the cell surface is a commonly observed phenomenon following agonist-stimulation. This process is now believed to be important for receptor resensitization as well as for signal transduction. Over the years, numerous studies have aimed at understanding the molecular mechanisms underlying internalization. Proteins such as the G protein-coupled receptor kinases (GRKs) and the beta-arrestins, which were initially characterized as desensitizing molecules, have been shown to be important regulators of the endocytic process. Recently, numerous interacting partners have been identified for each of these two classes of proteins. However, the details regarding the sequence of these interactions and the cross-talk between signaling pathways containing the different protein complexes are just beginning to be uncovered. In this review, we summarize these findings and discuss the role of GRKs and beta-arrestins, two families of key regulatory proteins that regulate G protein-coupled receptor endocytosis. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:61 / 79
页数:19
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