Diversity and specificity in the regulated endocytic membrane trafficking of G-protein-coupled receptors

被引:58
|
作者
Tsao, PI
von Zastrow, M
机构
[1] Univ Calif San Francisco, Dept Psychiat, Cell Biol Program, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Mol & Cellular Pharmacol, Cell Biol Program, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Biochem & Biophys, Cell Biol Program, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
G-protein; receptor; endocytosis; down-regulation; sorting; lysosomes;
D O I
10.1016/S0163-7258(00)00107-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Many G-protein-coupled receptors (GPCRs) an regulated by endocytosis. Pharmacological studies defining distinct processes of ligand-induced sequestration and down-regulation provided early evidence for significant complexity in the endocytic membrane trafficking of GPCRs, In this review, we discuss our present understanding of the diversity and specificity of GPCR endocytic membrane trafficking, focusing primarily on proteolytic down-regulation of GPCRs via delivery to lysosomes. U:e discuss evidence suggesting that certain GPCRs can be targeted selectively to lysosomes after endocytosis by the same membrane pathway that mediates the process of rapid sequestration, and we highlight recent progress in understanding a mechanism that controls the sorting of a specific GPCR between distinct membrane pathways after endocytosis by clathrin-coated pits. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:139 / 147
页数:9
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