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GPCR Signaling Regulation: The Role of GRKs and Arrestins

Every animal species expresses hundreds of different G protein-coupled receptors (GPCRs) that respond to a wide variety of external stimuli. GPCRs-driven signaling pathways are involved in pretty much every physiological function and in many pathologies. Therefore, GPCRs are targeted by about a thir...

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Autores principales: Gurevich, Vsevolod V., Gurevich, Eugenia V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389790/
https://www.ncbi.nlm.nih.gov/pubmed/30837883
http://dx.doi.org/10.3389/fphar.2019.00125
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author Gurevich, Vsevolod V.
Gurevich, Eugenia V.
author_facet Gurevich, Vsevolod V.
Gurevich, Eugenia V.
author_sort Gurevich, Vsevolod V.
collection PubMed
description Every animal species expresses hundreds of different G protein-coupled receptors (GPCRs) that respond to a wide variety of external stimuli. GPCRs-driven signaling pathways are involved in pretty much every physiological function and in many pathologies. Therefore, GPCRs are targeted by about a third of clinically used drugs. The signaling of most GPCRs via G proteins is terminated by the phosphorylation of active receptor by specific kinases (GPCR kinases, or GRKs) and subsequent binding of arrestin proteins, that selectively recognize active phosphorylated receptors. In addition, GRKs and arrestins play a role in multiple signaling pathways in the cell, both GPCR-initiated and receptor-independent. Here we focus on the mechanisms of GRK- and arrestin-mediated regulation of GPCR signaling, which includes homologous desensitization and redirection of signaling to additional pathways by bound arrestins.
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spelling pubmed-63897902019-03-05 GPCR Signaling Regulation: The Role of GRKs and Arrestins Gurevich, Vsevolod V. Gurevich, Eugenia V. Front Pharmacol Pharmacology Every animal species expresses hundreds of different G protein-coupled receptors (GPCRs) that respond to a wide variety of external stimuli. GPCRs-driven signaling pathways are involved in pretty much every physiological function and in many pathologies. Therefore, GPCRs are targeted by about a third of clinically used drugs. The signaling of most GPCRs via G proteins is terminated by the phosphorylation of active receptor by specific kinases (GPCR kinases, or GRKs) and subsequent binding of arrestin proteins, that selectively recognize active phosphorylated receptors. In addition, GRKs and arrestins play a role in multiple signaling pathways in the cell, both GPCR-initiated and receptor-independent. Here we focus on the mechanisms of GRK- and arrestin-mediated regulation of GPCR signaling, which includes homologous desensitization and redirection of signaling to additional pathways by bound arrestins. Frontiers Media S.A. 2019-02-19 /pmc/articles/PMC6389790/ /pubmed/30837883 http://dx.doi.org/10.3389/fphar.2019.00125 Text en Copyright © 2019 Gurevich and Gurevich. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Gurevich, Vsevolod V.
Gurevich, Eugenia V.
GPCR Signaling Regulation: The Role of GRKs and Arrestins
title GPCR Signaling Regulation: The Role of GRKs and Arrestins
title_full GPCR Signaling Regulation: The Role of GRKs and Arrestins
title_fullStr GPCR Signaling Regulation: The Role of GRKs and Arrestins
title_full_unstemmed GPCR Signaling Regulation: The Role of GRKs and Arrestins
title_short GPCR Signaling Regulation: The Role of GRKs and Arrestins
title_sort gpcr signaling regulation: the role of grks and arrestins
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389790/
https://www.ncbi.nlm.nih.gov/pubmed/30837883
http://dx.doi.org/10.3389/fphar.2019.00125
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