Membrane Trafficking of G Protein–Coupled Receptors

Christopher M. Tan(Vanderbilt University Medical Center), Ashley E. Brady(Vanderbilt University Medical Center), Hilary Highfield Nickols(Vanderbilt University Medical Center), Qin Wang(Vanderbilt University Medical Center), Lee E. Limbird(Vanderbilt University Medical Center)
The Annual Review of Pharmacology and Toxicology
January 27, 2004
Cited by 210

Abstract

G protein-coupled receptors (GPCRs) modulate diverse physiological and behavioral signaling pathways by virtue of changes in receptor activation and inactivation states. Functional changes in receptor properties include dynamic interactions with regulatory molecules and trafficking to various cellular compartments at various stages of the life cycle of a GPCR. This review focuses on trafficking of GPCRs to the cell surface, stabilization there, and agonist-regulated turnover. GPCR interactions with a variety of newly revealed partners also are reviewed with the intention of provoking further analysis of the relevance of these interactions in GPCR trafficking, signaling, or both. The disease consequences of mislocalization of GPCRs also are described.


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