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Designer Approaches for G Protein-Coupled Receptor Modulation for Cardiovascular Disease
被引:17
|作者:
Grisanti, Laurel A.
[1
,2
,3
]
Schumacher, Sarah M.
[1
,2
,4
]
Tilley, Douglas G.
[1
,2
]
Koch, Walter J.
[1
,2
]
机构:
[1] Temple Univ, Ctr Translat Med, Lewis Katz Sch Med, 3500 North Broad St,MERB 941, Philadelphia, PA 19140 USA
[2] Temple Univ, Dept Pharmacol, Lewis Katz Sch Med, Philadelphia, PA 19140 USA
[3] Univ Missouri, Dept Biomed Sci, Columbia, MO USA
[4] Cleveland Clin, Dept Mol Cardiol, Lerner Res Inst, Cleveland, OH 44106 USA
来源:
基金:
美国国家卫生研究院;
关键词:
biased ligands;
G protein-coupled receptor kinases;
G protein-coupled receptors;
D O I:
10.1016/j.jacbts.2017.12.002
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The new horizon for cardiac therapy may lie beneath the surface, with the downstream mediators of G protein-coupled receptor (GPCR) activity. Targeted approaches have shown that receptor activation may be biased toward signaling through G proteins or through GPCR kinases (GRKs) and beta-arrestins, with divergent functional outcomes. In addition to these canonical rotes, numerous noncanonical activities of GRKs and beta-arrestins have been demonstrated to modulate GPCR signaling at all levels of receptor activation and regulation. Further, research continues to identify novel GRK/effector and beta-arrestin/effector complexes with distinct impacts on cardiac function in the normal heart and the diseased heart. Coupled with the identification of once orphan receptors and endogenous ligands with beneficial cardiovascular effects, this expands the repertoire of GPCR targets. Together, this research highlights the potential for focused therapeutic activation of beneficial pathways, with simultaneous exclusion or inhibition of detrimental signaling, and represents a new wave of therapeutic development. (C) 2018 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.
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页码:550 / 562
页数:13
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