Regulation of GPCR anterograde trafficking by molecular chaperones and motifs

Brent Young, Jaime Wertman, Denis J. Dupré

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9 Citas (Scopus)

Resumen

G protein-coupled receptors (GPCRs) make up a superfamily of integral membrane proteins that respond to a wide variety of extracellular stimuli, giving them an important role in cell function and survival. They have also proven to be valuable targets in the fight against various diseases. As such, GPCR signal regulation has received considerable attention over the last few decades. With the amplitude of signaling being determined in large part by receptor density at the plasma membrane, several endogenous mechanisms for modulating GPCR expression at the cell surface have come to light. It has been shown that cell surface expression is determined by both exocytic and endocytic processes. However, the body of knowledge surrounding GPCR trafficking from the endoplasmic reticulum to the plasma membrane, commonly known as anterograde trafficking, has considerable room for growth. We focus here on the current paradigms of anterograde GPCR trafficking. We will discuss the regulatory role of both the general and "nonclassical private" chaperone systems in GPCR trafficking as well as conserved motifs that serve as modulators of GPCR export from the endoplasmic reticulum and Golgi apparatus. Together, these topics summarize some of the known mechanisms by which the cell regulates anterograde GPCR trafficking.

Idioma originalEnglish
Título de la publicación alojadaTrafficking of GPCRs, 2015
EditoresGuangyu Wu
EditorialElsevier B.V.
Páginas289-305
Número de páginas17
ISBN (versión impresa)9780128029398
DOI
EstadoPublished - 2015

Serie de la publicación

NombreProgress in Molecular Biology and Translational Science
Volumen132
ISSN (versión impresa)1877-1173
ISSN (versión digital)1878-0814

Nota bibliográfica

Funding Information:
B.Y. would like to acknowledge the Dalhousie Medical Research Foundation for funding via the Adopt-a-Researcher Program as well as Indspire for funding through the Health Careers Award program. J.W. acknowledges generous funding from the Killam Predoctoral Fellowship, the Dalhousie University President's Award, and the Scotia Scholar Award from the Nova Scotia Health Research Foundation. This work was supported by the Natural Sciences and Engineering Research Council of Canada to D.J.D. (NSERC Grant RGPIN-355310-2013).

Publisher Copyright:
© 2015 Elsevier Inc. All rights reserved.

ASJC Scopus Subject Areas

  • Molecular Medicine
  • Molecular Biology

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