doi: 10.1161/01.RES.0000158287.49872.4e
© 2005 American Heart Association, Inc.
Review |
Multi-Tasking RGS Proteins in the Heart
The Next Therapeutic Target?
From the Department of Pharmacology (E.L.R., P.A.I.), University of California San Diego, La Jolla; the Department of Physiology (R.A.S., M.B.), University of Maryland School of Medicine, Baltimore; and the Department of Molecular Cardiology (M.B.), Lerner Research Institute, The Cleveland Clinic Foundation, Ohio.
Correspondence to Meredith Bond, PhD, Department of Physiology, University of Maryland, 655 W Baltimore St, Baltimore, MD 21201. E-mail mbond001{at}umaryland.edu
This Review is part of a thematic series on Heterodimerization of Signaling Molecules, which includes the following articles:
Regulation of G Protein–Coupled Receptor Signaling By Scaffold Proteins
G Protein–Coupled Receptor Oligomerization: Implications for G Protein Activation and Cell Signaling
Multi-Tasking RGS Proteins in the Heart: The Next Therapeutic Target?
Gerda Breitwieser Editor
Regulator of G-protein–signaling (RGS) proteins play a key role in the regulation of G-protein–coupled receptor (GPCR) signaling. The characteristic hallmark of RGS proteins is a conserved 
120-aa RGS region that confers on these proteins the ability to serve as GTPase-activating proteins (GAPs) for G
proteins. Most RGS proteins can serve as GAPs for multiple isoforms of G and therefore have the potential to influence many cellular signaling pathways. However, RGS proteins can be highly regulated and can demonstrate extreme specificity for a particular signaling pathway. RGS proteins can be regulated by altering their GAP activity or subcellular localization; such regulation is achieved by phosphorylation, palmitoylation, and interaction with protein and lipid-binding partners. Many RGS proteins have GAP-independent functions that influence GPCR and non-GPCR–mediated signaling, such as effector regulation or action as an effector. Hence, RGS proteins should be considered multifunctional signaling regulators. GPCR-mediated signaling is critical for normal function in the cardiovascular system and is currently the primary target for the pharmacological treatment of disease. Alterations in RGS protein levels, in particular RGS2 and RGS4, produce cardiovascular phenotypes. Thus, because of the importance of GPCR-signaling pathways and the profound influence of RGS proteins on these pathways, RGS proteins are regulators of cardiovascular physiology and potentially novel drug targets as well.
Key Words: RGS protein • regulator of G-protein signaling • GPCRheart
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