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TGR5, Not Only a Metabolic Regulator

G-protein-coupled bile acid receptor, Gpbar1 (TGR5), is a member of G-protein-coupled receptor (GPCR) superfamily. High levels of TGR5 mRNA were detected in several tissues such as small intestine, stomach, liver, lung, especially in placenta and spleen. TGR5 is not only the receptor for bile acids,...

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Autores principales: Guo, Cong, Chen, Wei-Dong, Wang, Yan-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5183627/
https://www.ncbi.nlm.nih.gov/pubmed/28082913
http://dx.doi.org/10.3389/fphys.2016.00646
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author Guo, Cong
Chen, Wei-Dong
Wang, Yan-Dong
author_facet Guo, Cong
Chen, Wei-Dong
Wang, Yan-Dong
author_sort Guo, Cong
collection PubMed
description G-protein-coupled bile acid receptor, Gpbar1 (TGR5), is a member of G-protein-coupled receptor (GPCR) superfamily. High levels of TGR5 mRNA were detected in several tissues such as small intestine, stomach, liver, lung, especially in placenta and spleen. TGR5 is not only the receptor for bile acids, but also the receptor for multiple selective synthetic agonists such as 6α-ethyl-23(S)-methyl-cholic acid (6-EMCA, INT-777) and a series of 4-benzofuranyloxynicotinamde derivatives to regulate different signaling pathways such as nuclear factor κB (NF-κB), AKT, and extracellular signal-regulated kinases (ERK). TGR5, as a metabolic regulator, is involved in energy homeostasis, bile acid homeostasis, as well as glucose metabolism. More recently, our group and others have extended the functions of TGR5 to more than metabolic regulation, which include inflammatory response, cancer and liver regeneration. These findings highlight TGR5 as a potential drug target for different diseases. This review summarizes the basic information of TGR5 and its new functions.
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spelling pubmed-51836272017-01-12 TGR5, Not Only a Metabolic Regulator Guo, Cong Chen, Wei-Dong Wang, Yan-Dong Front Physiol Physiology G-protein-coupled bile acid receptor, Gpbar1 (TGR5), is a member of G-protein-coupled receptor (GPCR) superfamily. High levels of TGR5 mRNA were detected in several tissues such as small intestine, stomach, liver, lung, especially in placenta and spleen. TGR5 is not only the receptor for bile acids, but also the receptor for multiple selective synthetic agonists such as 6α-ethyl-23(S)-methyl-cholic acid (6-EMCA, INT-777) and a series of 4-benzofuranyloxynicotinamde derivatives to regulate different signaling pathways such as nuclear factor κB (NF-κB), AKT, and extracellular signal-regulated kinases (ERK). TGR5, as a metabolic regulator, is involved in energy homeostasis, bile acid homeostasis, as well as glucose metabolism. More recently, our group and others have extended the functions of TGR5 to more than metabolic regulation, which include inflammatory response, cancer and liver regeneration. These findings highlight TGR5 as a potential drug target for different diseases. This review summarizes the basic information of TGR5 and its new functions. Frontiers Media S.A. 2016-12-26 /pmc/articles/PMC5183627/ /pubmed/28082913 http://dx.doi.org/10.3389/fphys.2016.00646 Text en Copyright © 2016 Guo, Chen and Wang. 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) or licensor 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 Physiology
Guo, Cong
Chen, Wei-Dong
Wang, Yan-Dong
TGR5, Not Only a Metabolic Regulator
title TGR5, Not Only a Metabolic Regulator
title_full TGR5, Not Only a Metabolic Regulator
title_fullStr TGR5, Not Only a Metabolic Regulator
title_full_unstemmed TGR5, Not Only a Metabolic Regulator
title_short TGR5, Not Only a Metabolic Regulator
title_sort tgr5, not only a metabolic regulator
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5183627/
https://www.ncbi.nlm.nih.gov/pubmed/28082913
http://dx.doi.org/10.3389/fphys.2016.00646
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