GRKs and β-arrestins:: roles in receptor silencing, trafficking and signaling

被引:510
作者
Reiter, Eric
Lefkowitz, Robert J. [1 ]
机构
[1] Duke Univ, Ctr Med, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Ctr Med, Dept Biochem, Durham, NC 27710 USA
[3] Univ Tours, CNRS, INRA, UMR 6175, F-37380 Nouzilly, France
[4] Duke Univ, Ctr Med, Howard Hughes Med Inst, Durham, NC 27710 USA
关键词
D O I
10.1016/j.tem.2006.03.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Stimulation of cell-surface seven-transmembrane receptors (7TMRs) elicits biological responses to a wide range of extracellular signals, including many hormones. Classically, heterotrimeric GTP-binding proteins (G proteins) are recruited to the activated conformation of 7TMRs. Only two other families of protein have this remarkable characteristic: G-protein-coupled receptor kinases and P-arrestins. These two protein families have long been known to have a central and coordinated role in the 'desensitization' of G protein activation by 7TMRs. In addition, G-protein-coupled receptor kinases and beta-arrestins are involved in an increasing number of interactions with non-receptor proteins, broadening the variety of their cellular functions. These newly appreciated attributes of these two families of protein highlight their unique ability to coordinate the various aspects of 7TMR functions.
引用
收藏
页码:159 / 165
页数:7
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