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REV-ERBα regulates Fgf21 expression in the liver via hepatic nuclear factor 6
The circadian clock contributes to the timing of many body functions including metabolism and reproduction. The hepatokine fibroblast growth factor 21 (FGF21) is a critical metabolic regulator involved in modulation of fertility. Here we show that lack of the clock component REV-ERBα elevates FGF21...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278426/ https://www.ncbi.nlm.nih.gov/pubmed/27875243 http://dx.doi.org/10.1242/bio.021519 |
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author | Chavan, Rohit Preitner, Nadia Okabe, Takashi Strittmatter, Laureen Mansencal Xu, Cheng Ripperger, Jürgen A. Pitteloud, Nelly Albrecht, Urs |
author_facet | Chavan, Rohit Preitner, Nadia Okabe, Takashi Strittmatter, Laureen Mansencal Xu, Cheng Ripperger, Jürgen A. Pitteloud, Nelly Albrecht, Urs |
author_sort | Chavan, Rohit |
collection | PubMed |
description | The circadian clock contributes to the timing of many body functions including metabolism and reproduction. The hepatokine fibroblast growth factor 21 (FGF21) is a critical metabolic regulator involved in modulation of fertility. Here we show that lack of the clock component REV-ERBα elevates FGF21 levels in liver and plasma. At the molecular level, REV-ERBα modulates the expression of FGF21 via the liver-specific hepatic nuclear factor 6 (HNF6). We conclude that REV-ERBα regulates metabolism and reproduction, at least in part, via regulation of Fgf21. |
format | Online Article Text |
id | pubmed-5278426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52784262017-02-13 REV-ERBα regulates Fgf21 expression in the liver via hepatic nuclear factor 6 Chavan, Rohit Preitner, Nadia Okabe, Takashi Strittmatter, Laureen Mansencal Xu, Cheng Ripperger, Jürgen A. Pitteloud, Nelly Albrecht, Urs Biol Open Research Article The circadian clock contributes to the timing of many body functions including metabolism and reproduction. The hepatokine fibroblast growth factor 21 (FGF21) is a critical metabolic regulator involved in modulation of fertility. Here we show that lack of the clock component REV-ERBα elevates FGF21 levels in liver and plasma. At the molecular level, REV-ERBα modulates the expression of FGF21 via the liver-specific hepatic nuclear factor 6 (HNF6). We conclude that REV-ERBα regulates metabolism and reproduction, at least in part, via regulation of Fgf21. The Company of Biologists Ltd 2016-11-14 /pmc/articles/PMC5278426/ /pubmed/27875243 http://dx.doi.org/10.1242/bio.021519 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Chavan, Rohit Preitner, Nadia Okabe, Takashi Strittmatter, Laureen Mansencal Xu, Cheng Ripperger, Jürgen A. Pitteloud, Nelly Albrecht, Urs REV-ERBα regulates Fgf21 expression in the liver via hepatic nuclear factor 6 |
title | REV-ERBα regulates Fgf21 expression in the liver via hepatic nuclear factor 6 |
title_full | REV-ERBα regulates Fgf21 expression in the liver via hepatic nuclear factor 6 |
title_fullStr | REV-ERBα regulates Fgf21 expression in the liver via hepatic nuclear factor 6 |
title_full_unstemmed | REV-ERBα regulates Fgf21 expression in the liver via hepatic nuclear factor 6 |
title_short | REV-ERBα regulates Fgf21 expression in the liver via hepatic nuclear factor 6 |
title_sort | rev-erbα regulates fgf21 expression in the liver via hepatic nuclear factor 6 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278426/ https://www.ncbi.nlm.nih.gov/pubmed/27875243 http://dx.doi.org/10.1242/bio.021519 |
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