The G protein-coupled receptor kinase (GRK) interactome:: Role of GRKs in GPCR regulation and signaling

被引:301
作者
Ribas, Catalina
Penela, Petronila
Murga, Cristina
Salcedo, Alicia
Garcia-Hoz, Carlota
Jurado-Pueyo, Maria
Aymerich, Ivette
Mayor, Federico, Jr. [1 ]
机构
[1] Univ Autonoma Madrid, Ctr Biol Mol Severo Ochoa, CSIC, E-28049 Madrid, Spain
[2] Univ Autonoma Madrid, Dept Biol Mol, CSIC, E-28049 Madrid, Spain
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2007年 / 1768卷 / 04期
关键词
GRKs; GPCR; arrestin; G protein; kinase;
D O I
10.1016/j.bbamem.2006.09.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
G protein-coupled receptor kinases (GRKs) and arrestins are key participants in the canonical pathways leading to phosphorylation-dependent GPCR desensitization, endocytosis, intracellular trafficking and resensitization as well as in the modulation of important intracellular signaling cascades by GPCR. Novel studies have revealed a phosphorylation-independent desensitization mechanism operating through their RGS(RH) domain and the recent determination of the crystal structures of GRK2 and GRK6 has uncovered interesting details on the homology structure-function relationships of these kinases. Emerging evidence indicates that the activity of GRKs is tightly modulated by mechanisms including phosphorylation by different kinases and interaction with several cellular proteins such as calmodulin, caveolin or RKIP. In addition, GRKs are involved in multiple interactions with non-receptor proteins (PI3K, Akt, GIT or MEK) that point to novel GRK Cellular roles. In this article, our purpose is to describe the ever increasing map of functional interactions for GRK proteins as a basis to better understand its contribution to cellular processes. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:913 / 922
页数:10
相关论文
共 71 条
[1]  
CANT SH, 2005, MOL BIOL CELL
[2]   Regulation of G protein-coupled receptor kinases by caveolin [J].
Carman, CV ;
Lisanti, MP ;
Benovic, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (13) :8858-8864
[3]   Selective regulation of Gαq/11 by an RGS domain in the G protein-coupled receptor kinase, GRK2 [J].
Carman, CV ;
Parent, JL ;
Day, PW ;
Pronin, AN ;
Sternweis, PM ;
Wedegaertner, PB ;
Gilman, AG ;
Benovic, JL ;
Kozasa, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (48) :34483-34492
[4]   β-arrestin-mediated ADP-ribosylation factor 6 activation and β2-adrenergic receptor endocytosis [J].
Claing, A ;
Chen, W ;
Miller, WE ;
Vitale, N ;
Moss, J ;
Premont, RT ;
Lefkowitz, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (45) :42509-42513
[5]   G protein coupled receptor kinase-mediated desensitization of metabotropic glutamate receptor 1A protects against cell death [J].
Dale, LB ;
Bhattacharya, M ;
Anborgh, PH ;
Murdoch, B ;
Bhatia, M ;
Nakanishi, S ;
Ferguson, SSG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (49) :38213-38220
[6]   Differential interaction of GRK2 with members of the Gαq family [J].
Day, PW ;
Carman, CV ;
Sterne-Marr, R ;
Benovic, JL ;
Wedegaertner, PB .
BIOCHEMISTRY, 2003, 42 (30) :9176-9184
[7]   Phosphorylation-independent regulation of metabotropic glutamate receptor 1 signaling requires G protein-coupled receptor kinase 2 binding to the second intracellular loop [J].
Dhami, GK ;
Babwah, AV ;
Sterne-Marr, R ;
Ferguson, SSG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (26) :24420-24427
[8]   G protein-coupled receptor kinase 2 regulator of G protein signaling homology domain binds to both metabotropic glutamate receptor 1a and Gαq to attenuate signaling [J].
Dhami, GK ;
Dale, LB ;
Anborgh, PH ;
O'Connor-Halligan, KE ;
Sterne-Marr, R ;
Ferguson, SSG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (16) :16614-16620
[9]   Phosphorylation-independent regulation of metabotropic glutamate receptor signaling by G protein-coupled receptor kinase 2 [J].
Dhami, GK ;
Anborgh, PH ;
Dale, LB ;
Sterne-Marr, R ;
Ferguson, SSG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (28) :25266-25272
[10]   The amino-terminal domain of g-protein-coupled receptor kinase 2 is a regulatory gβγ binding site [J].
Eichmann, T ;
Lorenz, K ;
Hoffmann, M ;
Brockmann, J ;
Krasel, C ;
Lohse, MJ ;
Quitterer, U .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (10) :8052-8057