THE EVOLVING IMPACT OF G PROTEIN-COUPLED RECEPTOR KINASES IN CARDIAC HEALTH AND DISEASE

被引:114
作者
Sato, Priscila Y.
Chuprun, J. Kurt
Schwartz, Mathew
Koch, Walter J. [1 ]
机构
[1] Temple Univ, Sch Med, Dept Pharmacol, Philadelphia, PA 19140 USA
关键词
NF-KAPPA-B; LIGHT-DEPENDENT PHOSPHORYLATION; BETA-GAMMA-SUBUNITS; HEART-FAILURE; IN-VIVO; RHODOPSIN KINASE; TRANSGENIC MICE; HOMOLOGOUS DESENSITIZATION; MOLECULAR-CLONING; CRYSTAL-STRUCTURE;
D O I
10.1152/physrev.00015.2014
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
G protein-coupled receptors (GPCRs) are important regulators of various cellular functions via activation of intracellular signaling events. Active GPCR signaling is shut down by GPCR kinases (GRKs) and subsequent beta-arrestin-mediated mechanisms including phosphorylation, internalization, and either receptor degradation or resensitization. The seven-member GRK family varies in their structural composition, cellular localization, function, and mechanism of action (see sect. II). Here, we focus our attention on GRKs in particular canonical and novel roles of the GRKs found in the cardiovascular system (see sects. III and IV). Paramount to overall cardiac function is GPCR-mediated signaling provided by the adrenergic system. Overstimulation of the adrenergic system has been highly implicated in various etiologies of cardiovascular disease including hypertension and heart failure. GRKs acting downstream of heightened adrenergic signaling appear to be key players in cardiac homeostasis and disease progression, and herein we review the current data on GRKs related to cardiac disease and discuss their potential in the development of novel therapeutic strategies in cardiac diseases including heart failure.
引用
收藏
页码:377 / 404
页数:28
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