Literature DB >> 21605601

Intracellular α(2C)-adrenoceptors: storage depot, stunted development or signaling domain?

Maqsood A Chotani1, Nicholas A Flavahan.   

Abstract

G-protein coupled receptors (GPCRs) are generally considered to function as cell surface signaling structures that respond to extracellular mediators, many of which do not readily access the cell's interior. Indeed, most GPCRs are preferentially targeted to the plasma membrane. However, some receptors, including α(2C)-Adrenoceptors, challenge conventional concepts of GPCR activity by being preferentially retained and localized within intracellular organelles. This review will address the issues associated with this unusual GPCR localization and discuss whether it represents a novel sub-cellular niche for GPCR signaling, whether these receptors are being stored for rapid deployment to the cell surface, or whether they represent immature or incomplete receptor systems. 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21605601      PMCID: PMC3123388          DOI: 10.1016/j.bbamcr.2011.05.006

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  99 in total

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5.  Cloning and expression of a human kidney cDNA for an alpha 2-adrenergic receptor subtype.

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7.  Cyclic AMP-Rap1A signaling mediates cell surface translocation of microvascular smooth muscle α2C-adrenoceptors through the actin-binding protein filamin-2.

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8.  Delocalization of Endogenous A-kinase Antagonizes Rap1-Rho-α2C-Adrenoceptor Signaling in Human Microvascular Smooth Muscle Cells.

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