Abstract
Annual Review of Physiology
Vol. 68:
491-505
(Volume publication date January 2006)
(doi:10.1146/annurev.physiol.68.040104.131050)
First published online as a Review in Advance on August 18, 2005THE ASSOCIATION OF NHERF ADAPTOR PROTEINS WITH G PROTEIN–COUPLED RECEPTORS AND RECEPTOR TYROSINE KINASES *Edward J. Weinman,1 Randy A. Hall,2 Peter A. Friedman,3 Lee-Yuan Liu-Chen,4 and Shirish Shenolikar51Departments of Medicine and Physiology, University of Maryland School of Medicine, and Medical Service, Department of Veterans Affairs Medical Center, Baltimore, Maryland 21201; email: eweinman@medicine.umaryland.edu 2Department of Pharmacology, Rollins Research Center, Emory University School of Medicine, Atlanta, Georgia 30322; email: rhall@pharm.emory.edu 3Departments of Pharmacology and Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261; email: friedman@server.pharm.pitt.edu 4Department of Pharmacology and Center for Substance Abuse Research, Temple University School of Medicine, Philadelphia, Pennsylvania 19140; email: lliuche@astro.temple.edu 5Department Pharmacology and Cancer Biology, Duke University Medical Center, Durham, North Carolina 27710; email: sheno001@mc.duke.edu ▪ Abstract The sodium-hydrogen exchanger regulatory factors (NHERF-1 and NHERF-2) are a family of adaptor proteins characterized by the presence of two tandem PDZ protein interaction domains and a C-terminal domain that binds the cytoskeleton proteins ezrin, radixin, moesin, and merlin. The NHERF proteins are highly expressed in the kidney, small intestine, and other organs, where they associate with a number of transporters and ion channels, signaling proteins, and transcription factors. Recent evidence has revealed important associations between the NHERF proteins and several G protein–coupled receptors such as the β2-adrenergic receptor, the κ-opioid receptor, and the parathyroid hormone receptor, as well as growth factor tyrosine kinase receptors such as the platelet-derived growth factor receptor and the epidermal growth factor receptor. This review summarizes the emerging data on the biochemical mechanisms, physiologic outcomes, and potential clinical implications of the assembly and disassembly of receptor/NHERF complexes. Most recent citing papers (via CrossRef)Selectivity and functional consequences of interactions of family A G protein-coupled receptors with neurochondrin and periplakin Journal of Neurochemistry 109(1):182-192 (2009) DO WE NEED MOLECULAR TOMOGRAPHY OF A CELL AND HOW CAN IT BE ACHIEVED? Clinical and Experimental Pharmacology and Physiology 35(8):872-877 (2008) Kidney kinase network regulates renal ion cotransport Journal of Clinical Investigation 117(11):3179-3182 (2007)  Regulation of Receptor Trafficking by GRKs and Arrestins Annual Review of Physiology 69:451-482 (2007) Skeletal metastasis: Established and emerging roles of parathyroid hormone related protein (PTHrP) Cancer and Metastasis Reviews 25(4):559-571 (2007)
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