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Endomembrane-Based Signaling by GPCRs and G-Proteins

G-protein-coupled receptors (GPCRs) and G-proteins have a range of roles in many physiological and pathological processes and are among the most studied signaling proteins. A plethora of extracellular stimuli can activate the GPCR and can elicit distinct intracellular responses through the activatio...

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Detalles Bibliográficos
Autores principales: Liccardo, Federica, Luini, Alberto, Di Martino, Rosaria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8834376/
https://www.ncbi.nlm.nih.gov/pubmed/35159337
http://dx.doi.org/10.3390/cells11030528
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author Liccardo, Federica
Luini, Alberto
Di Martino, Rosaria
author_facet Liccardo, Federica
Luini, Alberto
Di Martino, Rosaria
author_sort Liccardo, Federica
collection PubMed
description G-protein-coupled receptors (GPCRs) and G-proteins have a range of roles in many physiological and pathological processes and are among the most studied signaling proteins. A plethora of extracellular stimuli can activate the GPCR and can elicit distinct intracellular responses through the activation of specific transduction pathways. For many years, biologists thought that GPCR signaling occurred entirely on the plasma membrane. However, in recent decades, many lines of evidence have proved that the GPCRs and G-proteins may reside on endomembranes and can start or propagate signaling pathways through the organelles that form the secretory route. How these alternative intracellular signaling pathways of the GPCR and G-proteins influence the physiological and pathological function of the endomembranes is still under investigation. Here, we review the general role and classification of GPCRs and G-proteins with a focus on their signaling pathways in the membrane transport apparatus.
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spelling pubmed-88343762022-02-12 Endomembrane-Based Signaling by GPCRs and G-Proteins Liccardo, Federica Luini, Alberto Di Martino, Rosaria Cells Review G-protein-coupled receptors (GPCRs) and G-proteins have a range of roles in many physiological and pathological processes and are among the most studied signaling proteins. A plethora of extracellular stimuli can activate the GPCR and can elicit distinct intracellular responses through the activation of specific transduction pathways. For many years, biologists thought that GPCR signaling occurred entirely on the plasma membrane. However, in recent decades, many lines of evidence have proved that the GPCRs and G-proteins may reside on endomembranes and can start or propagate signaling pathways through the organelles that form the secretory route. How these alternative intracellular signaling pathways of the GPCR and G-proteins influence the physiological and pathological function of the endomembranes is still under investigation. Here, we review the general role and classification of GPCRs and G-proteins with a focus on their signaling pathways in the membrane transport apparatus. MDPI 2022-02-03 /pmc/articles/PMC8834376/ /pubmed/35159337 http://dx.doi.org/10.3390/cells11030528 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Liccardo, Federica
Luini, Alberto
Di Martino, Rosaria
Endomembrane-Based Signaling by GPCRs and G-Proteins
title Endomembrane-Based Signaling by GPCRs and G-Proteins
title_full Endomembrane-Based Signaling by GPCRs and G-Proteins
title_fullStr Endomembrane-Based Signaling by GPCRs and G-Proteins
title_full_unstemmed Endomembrane-Based Signaling by GPCRs and G-Proteins
title_short Endomembrane-Based Signaling by GPCRs and G-Proteins
title_sort endomembrane-based signaling by gpcrs and g-proteins
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8834376/
https://www.ncbi.nlm.nih.gov/pubmed/35159337
http://dx.doi.org/10.3390/cells11030528
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