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GPR41 and GPR43 in Obesity and Inflammation – Protective or Causative?
GPR41 and GPR43 are a pair of mammalian G protein-coupled receptors (GPCRs) expressed in human adipocytes, colon epithelial cells, and peripheral blood mononuclear cells. These receptors are activated by short-chain fatty acids (SCFAs) such as acetate, propionate, and butyrate – which are produced d...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734206/ https://www.ncbi.nlm.nih.gov/pubmed/26870043 http://dx.doi.org/10.3389/fimmu.2016.00028 |
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author | Ang, Zhiwei Ding, Jeak Ling |
author_facet | Ang, Zhiwei Ding, Jeak Ling |
author_sort | Ang, Zhiwei |
collection | PubMed |
description | GPR41 and GPR43 are a pair of mammalian G protein-coupled receptors (GPCRs) expressed in human adipocytes, colon epithelial cells, and peripheral blood mononuclear cells. These receptors are activated by short-chain fatty acids (SCFAs) such as acetate, propionate, and butyrate – which are produced during dietary fiber fermentation by resident gut bacteria. This unique ligand specificity suggests that GPR41 and GPR43 may mediate the interaction between the human host and the gut microbiome. Indeed, studies on knockout mice implicate GPR41 and GPR43 in chronic inflammatory disorders such as obesity, colitis, asthma and arthritis. However, whether GPR41 and GPR43 are protective or causative is inconsistent between studies. This discrepancy may be due to differences in the disease models used, the inbred mouse strains, or non-specific knockout effects. Here, we review the latest findings on GPR41 and GPR43, highlighting contradictory observations. With GPR41 and GPR43 being considered as drug targets, it is pertinent that their role is fully elucidated. We propose that future studies on human tissues, ex vivo, may allow us to confirm the role of GPR41 and GPR43 in humans, be it protective or causative. |
format | Online Article Text |
id | pubmed-4734206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47342062016-02-11 GPR41 and GPR43 in Obesity and Inflammation – Protective or Causative? Ang, Zhiwei Ding, Jeak Ling Front Immunol Immunology GPR41 and GPR43 are a pair of mammalian G protein-coupled receptors (GPCRs) expressed in human adipocytes, colon epithelial cells, and peripheral blood mononuclear cells. These receptors are activated by short-chain fatty acids (SCFAs) such as acetate, propionate, and butyrate – which are produced during dietary fiber fermentation by resident gut bacteria. This unique ligand specificity suggests that GPR41 and GPR43 may mediate the interaction between the human host and the gut microbiome. Indeed, studies on knockout mice implicate GPR41 and GPR43 in chronic inflammatory disorders such as obesity, colitis, asthma and arthritis. However, whether GPR41 and GPR43 are protective or causative is inconsistent between studies. This discrepancy may be due to differences in the disease models used, the inbred mouse strains, or non-specific knockout effects. Here, we review the latest findings on GPR41 and GPR43, highlighting contradictory observations. With GPR41 and GPR43 being considered as drug targets, it is pertinent that their role is fully elucidated. We propose that future studies on human tissues, ex vivo, may allow us to confirm the role of GPR41 and GPR43 in humans, be it protective or causative. Frontiers Media S.A. 2016-02-01 /pmc/articles/PMC4734206/ /pubmed/26870043 http://dx.doi.org/10.3389/fimmu.2016.00028 Text en Copyright © 2016 Ang and Ding. 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 | Immunology Ang, Zhiwei Ding, Jeak Ling GPR41 and GPR43 in Obesity and Inflammation – Protective or Causative? |
title | GPR41 and GPR43 in Obesity and Inflammation – Protective or Causative? |
title_full | GPR41 and GPR43 in Obesity and Inflammation – Protective or Causative? |
title_fullStr | GPR41 and GPR43 in Obesity and Inflammation – Protective or Causative? |
title_full_unstemmed | GPR41 and GPR43 in Obesity and Inflammation – Protective or Causative? |
title_short | GPR41 and GPR43 in Obesity and Inflammation – Protective or Causative? |
title_sort | gpr41 and gpr43 in obesity and inflammation – protective or causative? |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734206/ https://www.ncbi.nlm.nih.gov/pubmed/26870043 http://dx.doi.org/10.3389/fimmu.2016.00028 |
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