Membrane trafficking of G protein-coupled receptors

被引:159
|
作者
Tan, CM [1 ]
Brady, AE [1 ]
Nickols, HH [1 ]
Wang, Q [1 ]
Limbird, LE [1 ]
机构
[1] Vanderbilt Univ, Ctr Med, Dept Pharmacol, Nashville, TN 37232 USA
关键词
protein-protein interactions; agonist-elicited endocytosis;
D O I
10.1146/annurev.pharmtox.44.101802.121558
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
G protein-coupled receptors (GPCRs) modulate diverse physiological and behavioral signaling pathways by virtue of changes in receptor activation and inactivation states. Functional changes in receptor properties include dynamic interactions with regulatory molecules and trafficking to various cellular compartments at various stages of the life cycle of a GPCR. This review focuses on trafficking of GPCRs to the cell surface, stabilization there, and agonist-regulated turnover. GPCR interactions with a variety of newly revealed partners also are reviewed with the intention of provoking further analysis of the relevance of these interactions in GPCR trafficking, signaling, or both. The disease consequences of mislocalization. of GPCRs also are described.
引用
收藏
页码:559 / 609
页数:51
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