| Literature DB >> 17482545 |
Erin J Whalen1, Matthew W Foster, Akio Matsumoto, Kentaro Ozawa, Jonathan D Violin, Loretta G Que, Chris D Nelson, Moran Benhar, Janelle R Keys, Howard A Rockman, Walter J Koch, Yehia Daaka, Robert J Lefkowitz, Jonathan S Stamler.
Abstract
beta-adrenergic receptors (beta-ARs), prototypic G-protein-coupled receptors (GPCRs), play a critical role in regulating numerous physiological processes. The GPCR kinases (GRKs) curtail G-protein signaling and target receptors for internalization. Nitric oxide (NO) and/or S-nitrosothiols (SNOs) can prevent the loss of beta-AR signaling in vivo, but the molecular details are unknown. Here we show in mice that SNOs increase beta-AR expression and prevent agonist-stimulated receptor downregulation; and in cells, SNOs decrease GRK2-mediated beta-AR phosphorylation and subsequent recruitment of beta-arrestin to the receptor, resulting in the attenuation of receptor desensitization and internalization. In both cells and tissues, GRK2 is S-nitrosylated by SNOs as well as by NO synthases, and GRK2 S-nitrosylation increases following stimulation of multiple GPCRs with agonists. Cys340 of GRK2 is identified as a principal locus of inhibition by S-nitrosylation. Our studies thus reveal a central molecular mechanism through which GPCR signaling is regulated.Entities:
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Year: 2007 PMID: 17482545 DOI: 10.1016/j.cell.2007.02.046
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582