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The α(1)-adrenergic receptors: diversity of signaling networks and regulation

The α(1)-adrenergic receptor (AR) subtypes (α(1a), α(1b), and α(1d)) mediate several physiological effects of epinephrineand norepinephrine. Despite several studies in recombinant systems and insightfrom genetically modified mice, our understanding of the physiological relevance and specificity of t...

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Detalles Bibliográficos
Autor principal: Cotecchia, Susanna
Formato: Texto
Lenguaje:English
Publicado: Informa Healthcare 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018134/
https://www.ncbi.nlm.nih.gov/pubmed/20954794
http://dx.doi.org/10.3109/10799893.2010.518152
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author Cotecchia, Susanna
author_facet Cotecchia, Susanna
author_sort Cotecchia, Susanna
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description The α(1)-adrenergic receptor (AR) subtypes (α(1a), α(1b), and α(1d)) mediate several physiological effects of epinephrineand norepinephrine. Despite several studies in recombinant systems and insightfrom genetically modified mice, our understanding of the physiological relevance and specificity of the α(1)-AR subtypes is still limited. Constitutive activity and receptor oligomerization have emerged as potential features regulating receptor function. Another recent paradigm is that βarrestins and G protein-coupled receptors themselves can act as scaffolds binding a variety of proteins and this can result in growing complexity of the receptor-mediated cellular effects. The aim of this review is to summarize our current knowledge on some recently identified functional paradigms and signaling networks that might help to elucidate the functional diversity of the α(1)-AR subtypes in various organs.
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spelling pubmed-30181342011-01-11 The α(1)-adrenergic receptors: diversity of signaling networks and regulation Cotecchia, Susanna J Recept Signal Transduct Res Review Article The α(1)-adrenergic receptor (AR) subtypes (α(1a), α(1b), and α(1d)) mediate several physiological effects of epinephrineand norepinephrine. Despite several studies in recombinant systems and insightfrom genetically modified mice, our understanding of the physiological relevance and specificity of the α(1)-AR subtypes is still limited. Constitutive activity and receptor oligomerization have emerged as potential features regulating receptor function. Another recent paradigm is that βarrestins and G protein-coupled receptors themselves can act as scaffolds binding a variety of proteins and this can result in growing complexity of the receptor-mediated cellular effects. The aim of this review is to summarize our current knowledge on some recently identified functional paradigms and signaling networks that might help to elucidate the functional diversity of the α(1)-AR subtypes in various organs. Informa Healthcare 2010-12 2010-10-18 /pmc/articles/PMC3018134/ /pubmed/20954794 http://dx.doi.org/10.3109/10799893.2010.518152 Text en © 2010 Informa Healthcare USA, Inc. http://creativecommons.org/licenses/by/2.0/ This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Informa Healthcare journals (http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Cotecchia, Susanna
The α(1)-adrenergic receptors: diversity of signaling networks and regulation
title The α(1)-adrenergic receptors: diversity of signaling networks and regulation
title_full The α(1)-adrenergic receptors: diversity of signaling networks and regulation
title_fullStr The α(1)-adrenergic receptors: diversity of signaling networks and regulation
title_full_unstemmed The α(1)-adrenergic receptors: diversity of signaling networks and regulation
title_short The α(1)-adrenergic receptors: diversity of signaling networks and regulation
title_sort α(1)-adrenergic receptors: diversity of signaling networks and regulation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018134/
https://www.ncbi.nlm.nih.gov/pubmed/20954794
http://dx.doi.org/10.3109/10799893.2010.518152
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