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FXR controls CHOP expression in steatohepatitis

The farnesoid X receptor (FXR) and C/EBP homologous protein (CHOP) have critical functions in hepatic lipid metabolism. Here, we aimed to explore a potential relationship between FXR and CHOP. We fed wild‐type (WT) and FXR KO mice a MCD diet (model of steatohepatitis) and found that Chop mRNA expres...

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Autores principales: Fuchs, Claudia D., Claudel, Thierry, Scharnagl, Hubert, Stojakovic, Tatjana, Trauner, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698708/
https://www.ncbi.nlm.nih.gov/pubmed/28895119
http://dx.doi.org/10.1002/1873-3468.12845
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author Fuchs, Claudia D.
Claudel, Thierry
Scharnagl, Hubert
Stojakovic, Tatjana
Trauner, Michael
author_facet Fuchs, Claudia D.
Claudel, Thierry
Scharnagl, Hubert
Stojakovic, Tatjana
Trauner, Michael
author_sort Fuchs, Claudia D.
collection PubMed
description The farnesoid X receptor (FXR) and C/EBP homologous protein (CHOP) have critical functions in hepatic lipid metabolism. Here, we aimed to explore a potential relationship between FXR and CHOP. We fed wild‐type (WT) and FXR KO mice a MCD diet (model of steatohepatitis) and found that Chop mRNA expression is upregulated in WT but not FXR KO mice. The absence of FXR aggravates hepatic inflammation after MCD feeding. In HepG2 cells, we found that Chop expression is regulated in a FXR/Retinoid X receptor (RXR)‐dependent manner. We identified a FXR/RXR‐binding site in the human CHOP promoter, demonstrating a highly conserved regulatory pathway. Our study shows that FXR/RXR regulates Chop expression in a mouse model of steatohepatitis, providing novel insights into pathogenesis of this disorder.
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spelling pubmed-56987082017-11-28 FXR controls CHOP expression in steatohepatitis Fuchs, Claudia D. Claudel, Thierry Scharnagl, Hubert Stojakovic, Tatjana Trauner, Michael FEBS Lett Research Letters The farnesoid X receptor (FXR) and C/EBP homologous protein (CHOP) have critical functions in hepatic lipid metabolism. Here, we aimed to explore a potential relationship between FXR and CHOP. We fed wild‐type (WT) and FXR KO mice a MCD diet (model of steatohepatitis) and found that Chop mRNA expression is upregulated in WT but not FXR KO mice. The absence of FXR aggravates hepatic inflammation after MCD feeding. In HepG2 cells, we found that Chop expression is regulated in a FXR/Retinoid X receptor (RXR)‐dependent manner. We identified a FXR/RXR‐binding site in the human CHOP promoter, demonstrating a highly conserved regulatory pathway. Our study shows that FXR/RXR regulates Chop expression in a mouse model of steatohepatitis, providing novel insights into pathogenesis of this disorder. John Wiley and Sons Inc. 2017-10-11 2017-10 /pmc/articles/PMC5698708/ /pubmed/28895119 http://dx.doi.org/10.1002/1873-3468.12845 Text en © 2017 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Letters
Fuchs, Claudia D.
Claudel, Thierry
Scharnagl, Hubert
Stojakovic, Tatjana
Trauner, Michael
FXR controls CHOP expression in steatohepatitis
title FXR controls CHOP expression in steatohepatitis
title_full FXR controls CHOP expression in steatohepatitis
title_fullStr FXR controls CHOP expression in steatohepatitis
title_full_unstemmed FXR controls CHOP expression in steatohepatitis
title_short FXR controls CHOP expression in steatohepatitis
title_sort fxr controls chop expression in steatohepatitis
topic Research Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698708/
https://www.ncbi.nlm.nih.gov/pubmed/28895119
http://dx.doi.org/10.1002/1873-3468.12845
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