GRK mythology: G-protein receptor kinases in cardiovascular disease

被引:86
作者
Dorn, Gerald W., II [1 ]
机构
[1] Washington Univ, Ctr Pharmacogenom, St Louis, MO 63110 USA
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2009年 / 87卷 / 05期
关键词
G-protein receptor kinases; Adrenergic receptors; Cell signaling; Myocardial infarction; Heart failure; BETA-ARRESTIN; HEART-FAILURE; BETA-ARK1; INHIBITION; SELECTIVE REGULATION; CARDIAC-FUNCTION; EGF RECEPTOR; GENE-THERAPY; EXPRESSION; TRANSACTIVATION; DESENSITIZATION;
D O I
10.1007/s00109-009-0450-7
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
G-protein receptor kinases (GRKs) are indispensable for terminating signaling of G-protein coupled receptors (GPCR) through receptor desensitization and downregulation. Increased neurohormone levels in heart failure and the adverse consequences of constant neurohormonal stimulation suggest an important protective role for mechanisms that desensitize neurohormone receptor responses. For that reason, GRK2, the first GRK identified in the heart, has been extensively studied in heart failure, cardiac hypertrophy, and myocardial infarction. However, our understanding of the roles of GRKs in general, and the differential effects of cardiac receptor phosphorylation by individual cardiac-expressed GRKs, have evolved considerably in the last few years. Here, recent developments are reviewed, with an emphasis on novel GRK functions and signaling pathways.
引用
收藏
页码:455 / 463
页数:9
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