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Metabolite-sensing GPCRs controlling interactions between adipose tissue and inflammation
Metabolic disorders including obesity, diabetes and non-alcoholic steatohepatitis are a group of conditions characterised by chronic low-grade inflammation of metabolic tissues. There is now a growing appreciation that various metabolites released from adipose tissue serve as key signalling mediator...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357040/ https://www.ncbi.nlm.nih.gov/pubmed/37484963 http://dx.doi.org/10.3389/fendo.2023.1197102 |
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author | Duncan, Elaine M. Vita, Luca Dibnah, Bethany Hudson, Brian D. |
author_facet | Duncan, Elaine M. Vita, Luca Dibnah, Bethany Hudson, Brian D. |
author_sort | Duncan, Elaine M. |
collection | PubMed |
description | Metabolic disorders including obesity, diabetes and non-alcoholic steatohepatitis are a group of conditions characterised by chronic low-grade inflammation of metabolic tissues. There is now a growing appreciation that various metabolites released from adipose tissue serve as key signalling mediators, influencing this interaction with inflammation. G protein-coupled receptors (GPCRs) are the largest family of signal transduction proteins and most historically successful drug targets. The signalling pathways for several key adipose metabolites are mediated through GPCRs expressed both on the adipocytes themselves and on infiltrating macrophages. These include three main groups of GPCRs: the FFA4 receptor, which is activated by long chain free fatty acids; the HCA(2) and HCA(3) receptors, activated by hydroxy carboxylic acids; and the succinate receptor. Understanding the roles these metabolites and their receptors play in metabolic-immune interactions is critical to establishing how these GPCRs may be exploited for the treatment of metabolic disorders. |
format | Online Article Text |
id | pubmed-10357040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103570402023-07-21 Metabolite-sensing GPCRs controlling interactions between adipose tissue and inflammation Duncan, Elaine M. Vita, Luca Dibnah, Bethany Hudson, Brian D. Front Endocrinol (Lausanne) Endocrinology Metabolic disorders including obesity, diabetes and non-alcoholic steatohepatitis are a group of conditions characterised by chronic low-grade inflammation of metabolic tissues. There is now a growing appreciation that various metabolites released from adipose tissue serve as key signalling mediators, influencing this interaction with inflammation. G protein-coupled receptors (GPCRs) are the largest family of signal transduction proteins and most historically successful drug targets. The signalling pathways for several key adipose metabolites are mediated through GPCRs expressed both on the adipocytes themselves and on infiltrating macrophages. These include three main groups of GPCRs: the FFA4 receptor, which is activated by long chain free fatty acids; the HCA(2) and HCA(3) receptors, activated by hydroxy carboxylic acids; and the succinate receptor. Understanding the roles these metabolites and their receptors play in metabolic-immune interactions is critical to establishing how these GPCRs may be exploited for the treatment of metabolic disorders. Frontiers Media S.A. 2023-07-06 /pmc/articles/PMC10357040/ /pubmed/37484963 http://dx.doi.org/10.3389/fendo.2023.1197102 Text en Copyright © 2023 Duncan, Vita, Dibnah and Hudson https://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 | Endocrinology Duncan, Elaine M. Vita, Luca Dibnah, Bethany Hudson, Brian D. Metabolite-sensing GPCRs controlling interactions between adipose tissue and inflammation |
title | Metabolite-sensing GPCRs controlling interactions between adipose tissue and inflammation |
title_full | Metabolite-sensing GPCRs controlling interactions between adipose tissue and inflammation |
title_fullStr | Metabolite-sensing GPCRs controlling interactions between adipose tissue and inflammation |
title_full_unstemmed | Metabolite-sensing GPCRs controlling interactions between adipose tissue and inflammation |
title_short | Metabolite-sensing GPCRs controlling interactions between adipose tissue and inflammation |
title_sort | metabolite-sensing gpcrs controlling interactions between adipose tissue and inflammation |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357040/ https://www.ncbi.nlm.nih.gov/pubmed/37484963 http://dx.doi.org/10.3389/fendo.2023.1197102 |
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