G Protein Coupled Receptor Kinases as Therapeutic Targets in Cardiovascular Disease

被引:130
作者
Belmonte, Stephen L. [1 ]
Blaxall, Burns C. [1 ]
机构
[1] Univ Rochester, Sch Med & Dent, Aab Cardiovasc Res Inst, Dept Med,Med Ctr, Rochester, NY 14642 USA
关键词
G protein-coupled receptors; G protein-coupled receptor kinases; heart failure; adrenergic receptors; cardiovascular disease; G-BETA-GAMMA; CONGESTIVE-HEART-FAILURE; FAILING HUMAN HEART; ANGIOTENSIN-II RECEPTOR; SMOOTH-MUSCLE-CELLS; LOW SODIUM DIET; TRANSGENIC MICE; GENE-TRANSFER; CARDIAC-HYPERTROPHY; ADRENERGIC RESPONSIVENESS;
D O I
10.1161/CIRCRESAHA.110.231233
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
G protein-coupled receptors (GPCRs) represent the largest family of membrane receptors and are responsible for regulating a wide variety of physiological processes. This is accomplished via ligand binding to GPCRs, activating associated heterotrimeric G proteins and intracellular signaling pathways. G protein-coupled receptor kinases (GRKs), in concert with beta-arrestins, classically desensitize receptor signal transduction, thus preventing hyperactivation of GPCR second-messenger cascades. As changes in GRK expression have featured prominently in many cardiovascular pathologies, including heart failure, myocardial infarction, hypertension, and cardiac hypertrophy, GRKs have been intensively studied as potential diagnostic or therapeutic targets. Herein, we review our evolving understanding of the role of GRKs in cardiovascular pathophysiology. (Circ Res. 2011; 109: 309-319.)
引用
收藏
页码:309 / 319
页数:11
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