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Location, location, location…site-specific GPCR phosphorylation offers a mechanism for cell-type-specific signalling

It is now established that most of the ∼800 G-protein-coupled receptors (GPCRs) are regulated by phosphorylation in a process that results in the recruitment of arrestins, leading to receptor desensitization and the activation of arrestin-dependent processes. This generalized view of GPCR regulation...

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Detalles Bibliográficos
Autores principales: Tobin, Andrew B., Butcher, Adrian J., Kong, Kok Choi
Formato: Texto
Lenguaje:English
Publicado: Published By Elsevier In Association With The International Union Of Pharmacology 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2880250/
https://www.ncbi.nlm.nih.gov/pubmed/18606460
http://dx.doi.org/10.1016/j.tips.2008.05.006
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author Tobin, Andrew B.
Butcher, Adrian J.
Kong, Kok Choi
author_facet Tobin, Andrew B.
Butcher, Adrian J.
Kong, Kok Choi
author_sort Tobin, Andrew B.
collection PubMed
description It is now established that most of the ∼800 G-protein-coupled receptors (GPCRs) are regulated by phosphorylation in a process that results in the recruitment of arrestins, leading to receptor desensitization and the activation of arrestin-dependent processes. This generalized view of GPCR regulation, however, does not provide an adequate mechanism for the control of tissue-specific GPCR signalling. Here, we review the evidence that GPCR phosphorylation is, in fact, a flexible and dynamic regulatory process in which GPCRs are phosphorylated in a unique manner that is associated with the cell type in which the receptor is expressed. In this scenario, phosphorylation offers a mechanism of regulating the signalling outcome of GPCRs that can be tailored to meet a specific physiological role.
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spelling pubmed-28802502010-07-09 Location, location, location…site-specific GPCR phosphorylation offers a mechanism for cell-type-specific signalling Tobin, Andrew B. Butcher, Adrian J. Kong, Kok Choi Trends Pharmacol Sci Review It is now established that most of the ∼800 G-protein-coupled receptors (GPCRs) are regulated by phosphorylation in a process that results in the recruitment of arrestins, leading to receptor desensitization and the activation of arrestin-dependent processes. This generalized view of GPCR regulation, however, does not provide an adequate mechanism for the control of tissue-specific GPCR signalling. Here, we review the evidence that GPCR phosphorylation is, in fact, a flexible and dynamic regulatory process in which GPCRs are phosphorylated in a unique manner that is associated with the cell type in which the receptor is expressed. In this scenario, phosphorylation offers a mechanism of regulating the signalling outcome of GPCRs that can be tailored to meet a specific physiological role. Published By Elsevier In Association With The International Union Of Pharmacology 2008-08 /pmc/articles/PMC2880250/ /pubmed/18606460 http://dx.doi.org/10.1016/j.tips.2008.05.006 Text en © 2008 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Review
Tobin, Andrew B.
Butcher, Adrian J.
Kong, Kok Choi
Location, location, location…site-specific GPCR phosphorylation offers a mechanism for cell-type-specific signalling
title Location, location, location…site-specific GPCR phosphorylation offers a mechanism for cell-type-specific signalling
title_full Location, location, location…site-specific GPCR phosphorylation offers a mechanism for cell-type-specific signalling
title_fullStr Location, location, location…site-specific GPCR phosphorylation offers a mechanism for cell-type-specific signalling
title_full_unstemmed Location, location, location…site-specific GPCR phosphorylation offers a mechanism for cell-type-specific signalling
title_short Location, location, location…site-specific GPCR phosphorylation offers a mechanism for cell-type-specific signalling
title_sort location, location, location…site-specific gpcr phosphorylation offers a mechanism for cell-type-specific signalling
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2880250/
https://www.ncbi.nlm.nih.gov/pubmed/18606460
http://dx.doi.org/10.1016/j.tips.2008.05.006
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