Constitutive desensitization: A new paradigm for G protein-coupled receptor regulation

被引:23
作者
Barak, LS
Wilbanks, AM
Caron, MG [1 ]
机构
[1] Duke Univ, Med Ctr, Howard Hughes Med Inst, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
关键词
D O I
10.1089/15406580360545152
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
GPCRs are a large family of cell-surface proteins that regulate many important biochemical pathways and physiological responses. The isolation and characterization of GPCRs represent one of the more remarkable success stories that occurred during the revolution in biology of the last quarter century. Of the many discoveries that originated in the laboratory of Robert Lefkowitz at Duke University concerning GPCR regulation, none is more fundamental than the elucidation of the families of GRKs and arrestin proteins that terminate GPCR signaling. In this essay, we will discuss how advances in microscopy and biology have made the visualization of GPCR, GRK, and arrestin activity possible in single cells. Additionally, we will discuss how imaging studies using arrestins and a naturally occurring mutant of the vasopressin receptor led to the recognition of a novel phenotypic receptor behavior, in which the receptor desensitizes in the absence of agonist. We have termed this process constitutive desensitization, and this unexpected receptor property suggests that it may be possible to develop novel classes of signal-inhibiting drugs distinct from conventional antagonists.
引用
收藏
页码:339 / 346
页数:8
相关论文
共 39 条
[21]   The superfamily of heptahelical receptors [J].
Lefkowitz, RJ .
NATURE CELL BIOLOGY, 2000, 2 (07) :E133-E136
[22]   G protein-coupled receptors III.: New roles for receptor kinases and β-arrestins in receptor signaling and desensitization [J].
Lefkowitz, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (30) :18677-18680
[23]   BETA-ARRESTIN - A PROTEIN THAT REGULATES BETA-ADRENERGIC-RECEPTOR FUNCTION [J].
LOHSE, MJ ;
BENOVIC, JL ;
CODINA, J ;
CARON, MG ;
LEFKOWITZ, RJ .
SCIENCE, 1990, 248 (4962) :1547-1550
[24]   Constitutively active alpha-1b adrenergic receptor mutants display different phosphorylation and internalization features [J].
Mhaouty-Kodja, S ;
Barak, LS ;
Scheer, A ;
Abuin, L ;
Diviani, D ;
Caron, MG ;
Cotecchia, S .
MOLECULAR PHARMACOLOGY, 1999, 55 (02) :339-347
[25]   The cellular distribution of fluorescently labeled arrestins provides a robust, sensitive, and universal assay for screening G protein-coupled receptors [J].
Oakley, RH ;
Hudson, CC ;
Cruickshank, RD ;
Meyers, DM ;
Payne, RE ;
Rhem, SM ;
Loomis, CR .
ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2002, 1 (01) :21-30
[26]   Molecular determinants underlying the formation of stable intracellular G protein-coupled receptor-β-arrestin complexes after receptor endocytosis [J].
Oakley, RH ;
Laporte, SA ;
Holt, JA ;
Barak, LS ;
Caron, MG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (22) :19452-19460
[27]   Association of β-arrestin with G protein-coupled receptors during clathrin-mediated endocytosis dictates the profile of receptor resensitization [J].
Oakley, RH ;
Laporte, SA ;
Holt, JA ;
Barak, LS ;
Caron, MG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (45) :32248-32257
[28]  
ODOWD BF, 1989, ANNU REV NEUROSCI, V12, P67, DOI 10.1146/annurev.neuro.12.1.67
[29]   PROTEIN-KINASES .3. PROTEIN-KINASES THAT PHOSPHORYLATE ACTIVATED G-PROTEIN COUPLED RECEPTORS [J].
PREMONT, RT ;
INGLESE, J ;
LEFKOWITZ, RJ .
FASEB JOURNAL, 1995, 9 (02) :175-182
[30]   SEQUENCE ALIGNMENT OF THE G-PROTEIN COUPLED RECEPTOR SUPERFAMILY [J].
PROBST, WC ;
SNYDER, LA ;
SCHUSTER, DI ;
BROSIUS, J ;
SEALFON, SC .
DNA AND CELL BIOLOGY, 1992, 11 (01) :1-20