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PMID: 19103204 Published · ppublish English Journal Article Review

Physiologic and cardiac roles of beta-arrestins.

Journal of molecular and cellular cardiology ·Vol. 46 ·No. 3 ·2009-03-00 ·Pages 300-8

Patel PA, Tilley DG, Rockman HA

Abstract

Beta-arrestin1 and beta-arrestin2 were initially identified by sequence homology to visual arrestins and by their ability to bind to and inactivate signaling of the beta-2-adrenergic receptor in a process known as desensitization. While the role of beta-arrestins in desensitization has been known for some time, more recent evidence has revealed that beta-arrestins are multifunctional scaffolding proteins that are involved in numerous aspects of G protein-coupled receptor (GPCR) signaling. Interestingly, exciting new data shows that beta-arrestins can mediate signaling in their own right independent of classical second messenger mediated signaling, and that this beta-arrestin-mediated signaling may be cardioprotective. Identifying novel ligands for GPCRs that can block G protein-mediated signaling while simultaneously promoting beta-arrestin-mediated signaling could provide powerful new therapies for cardiac disease.

MeSH Terms
Adrenergic beta-2 Receptor Agonists Animals Arrestins/metabolism Cardiotonic Agents/metabolism Heart Diseases/drug therapy,metabolism Humans Myocardium/metabolism Portraits as Topic Receptors, Adrenergic, beta-2/metabolism Second Messenger Systems beta-Arrestins
Chemicals
Adrenergic beta-2 Receptor Agonists Arrestins Cardiotonic Agents Receptors, Adrenergic, beta-2 beta-Arrestins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Patel Priyesh A
Duke University School of Medicine, Durham, North Carolina 27710, USA.
Tilley Douglas G
Rockman Howard A
Article Info
Journal
Journal of molecular and cellular cardiology
Abbr.
J Mol Cell Cardiol
ISSN
1095-8584
Published
2009-03-00
Epub
2008-00-06
Pages
300-8
Language
English
Region
England
NLM ID
0262322
Subset
IM
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