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Identification of miR-26a as a Target Gene of Bile Acid Receptor GPBAR-1/TGR5
GPBAR1/TGR5 is a G protein–coupled receptor of bile acids. TGR5 is known to regulate the BA homeostasis and energy metabolism. Recent studies highlight an important role of TGR5 in alleviating obesity and improving glucose regulation, however, the mechanism of which is still unclear. Here we report...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481113/ https://www.ncbi.nlm.nih.gov/pubmed/26107166 http://dx.doi.org/10.1371/journal.pone.0131294 |
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author | Chen, Xiaosong Xu, Haixia Ding, Lili Lou, Guiyu Liu, Yan Yao, Yalan Chen, Liangwan Huang, Wendong Fu, Xianghui |
author_facet | Chen, Xiaosong Xu, Haixia Ding, Lili Lou, Guiyu Liu, Yan Yao, Yalan Chen, Liangwan Huang, Wendong Fu, Xianghui |
author_sort | Chen, Xiaosong |
collection | PubMed |
description | GPBAR1/TGR5 is a G protein–coupled receptor of bile acids. TGR5 is known to regulate the BA homeostasis and energy metabolism. Recent studies highlight an important role of TGR5 in alleviating obesity and improving glucose regulation, however, the mechanism of which is still unclear. Here we report that TGR5 is involved in mediating the anti-obesity and anti-hyperglycemia effect of a natural compound, oleanolic acid. By comparing the miRNA profiles between wild type and TGR5(-/-) livers after OA treatment, we identified miR-26a as a novel downstream target gene of TGR5 activation. The expression of miR-26a in the liver was induced in a TGR5-dependent manner after feeding the mice with a bile acid diet. TGR5 activation strongly increased the expression of miR-26a in macrophages, including the Kupffer cells in the liver. We further demonstrated that JNK pathway was required for miR-26a induction by TGR5 activation. Interestingly, we located the TGR5-responsive DNA element to a proximal region of miR-26’s promoter, which was independent of the transcription of its host genes. These results unravel a new mechanism by which bile acid receptor TGR5 activates a miRNA gene expression. |
format | Online Article Text |
id | pubmed-4481113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44811132015-06-29 Identification of miR-26a as a Target Gene of Bile Acid Receptor GPBAR-1/TGR5 Chen, Xiaosong Xu, Haixia Ding, Lili Lou, Guiyu Liu, Yan Yao, Yalan Chen, Liangwan Huang, Wendong Fu, Xianghui PLoS One Research Article GPBAR1/TGR5 is a G protein–coupled receptor of bile acids. TGR5 is known to regulate the BA homeostasis and energy metabolism. Recent studies highlight an important role of TGR5 in alleviating obesity and improving glucose regulation, however, the mechanism of which is still unclear. Here we report that TGR5 is involved in mediating the anti-obesity and anti-hyperglycemia effect of a natural compound, oleanolic acid. By comparing the miRNA profiles between wild type and TGR5(-/-) livers after OA treatment, we identified miR-26a as a novel downstream target gene of TGR5 activation. The expression of miR-26a in the liver was induced in a TGR5-dependent manner after feeding the mice with a bile acid diet. TGR5 activation strongly increased the expression of miR-26a in macrophages, including the Kupffer cells in the liver. We further demonstrated that JNK pathway was required for miR-26a induction by TGR5 activation. Interestingly, we located the TGR5-responsive DNA element to a proximal region of miR-26’s promoter, which was independent of the transcription of its host genes. These results unravel a new mechanism by which bile acid receptor TGR5 activates a miRNA gene expression. Public Library of Science 2015-06-24 /pmc/articles/PMC4481113/ /pubmed/26107166 http://dx.doi.org/10.1371/journal.pone.0131294 Text en © 2015 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chen, Xiaosong Xu, Haixia Ding, Lili Lou, Guiyu Liu, Yan Yao, Yalan Chen, Liangwan Huang, Wendong Fu, Xianghui Identification of miR-26a as a Target Gene of Bile Acid Receptor GPBAR-1/TGR5 |
title | Identification of miR-26a as a Target Gene of Bile Acid Receptor GPBAR-1/TGR5 |
title_full | Identification of miR-26a as a Target Gene of Bile Acid Receptor GPBAR-1/TGR5 |
title_fullStr | Identification of miR-26a as a Target Gene of Bile Acid Receptor GPBAR-1/TGR5 |
title_full_unstemmed | Identification of miR-26a as a Target Gene of Bile Acid Receptor GPBAR-1/TGR5 |
title_short | Identification of miR-26a as a Target Gene of Bile Acid Receptor GPBAR-1/TGR5 |
title_sort | identification of mir-26a as a target gene of bile acid receptor gpbar-1/tgr5 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481113/ https://www.ncbi.nlm.nih.gov/pubmed/26107166 http://dx.doi.org/10.1371/journal.pone.0131294 |
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