Regulation of bile acid receptor activity

Many receptors can be activated by bile acids (BAs) and their derivatives. These include nuclear receptors farnesoid X receptor (FXR), pregnane X receptor (PXR), and vitamin D receptor (VDR), as well as membrane receptors Takeda G protein receptor 5 (TGR5), sphingosine-1-phosphate receptor 2 (S1PR2)...

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Main Authors: Yu-Jui Yvonne Wan, Lili Sheng
Format: Article
Language:English
Published: KeAi Communications Co., Ltd. 2018-12-01
Series:Liver Research
Online Access:http://www.sciencedirect.com/science/article/pii/S2542568418300278
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spelling doaj-27b4da267c514e98a0753ee9e1c1b3372021-02-02T06:49:05ZengKeAi Communications Co., Ltd.Liver Research2542-56842018-12-0124180185Regulation of bile acid receptor activityYu-Jui Yvonne Wan0Lili Sheng1Corresponding author.; Department of Medical Pathology and Laboratory Medicine, University of California, Davis, Sacramento, CA, USADepartment of Medical Pathology and Laboratory Medicine, University of California, Davis, Sacramento, CA, USAMany receptors can be activated by bile acids (BAs) and their derivatives. These include nuclear receptors farnesoid X receptor (FXR), pregnane X receptor (PXR), and vitamin D receptor (VDR), as well as membrane receptors Takeda G protein receptor 5 (TGR5), sphingosine-1-phosphate receptor 2 (S1PR2), and cholinergic receptor muscarinic 2 (CHRM2). All of them are implicated in the development of metabolic and immunological diseases in response to endobiotic and xenobiotic exposure. Because epigenetic regulation is critical for organisms to adapt to constant environmental changes, this review article summarizes epigenetic regulation as well as post-transcriptional modification of bile acid receptors. In addition, the focus of this review is on the liver and digestive tract although these receptors may have effects on other organs. Those regulatory mechanisms are implicated in the disease process and critically important in uncovering innovative strategy for prevention and treatment of metabolic and immunological diseases. Keywords: Bile acid receptor, Farnesoid X receptor (FXR), G protein-coupled bile acid receptor, Takeda G protein receptor 5 (TGR5), Sphingosine-1-phosphate receptor 2 (S1PR2), Acetylation, Methylation, Glycosylationhttp://www.sciencedirect.com/science/article/pii/S2542568418300278
collection DOAJ
language English
format Article
sources DOAJ
author Yu-Jui Yvonne Wan
Lili Sheng
spellingShingle Yu-Jui Yvonne Wan
Lili Sheng
Regulation of bile acid receptor activity
Liver Research
author_facet Yu-Jui Yvonne Wan
Lili Sheng
author_sort Yu-Jui Yvonne Wan
title Regulation of bile acid receptor activity
title_short Regulation of bile acid receptor activity
title_full Regulation of bile acid receptor activity
title_fullStr Regulation of bile acid receptor activity
title_full_unstemmed Regulation of bile acid receptor activity
title_sort regulation of bile acid receptor activity
publisher KeAi Communications Co., Ltd.
series Liver Research
issn 2542-5684
publishDate 2018-12-01
description Many receptors can be activated by bile acids (BAs) and their derivatives. These include nuclear receptors farnesoid X receptor (FXR), pregnane X receptor (PXR), and vitamin D receptor (VDR), as well as membrane receptors Takeda G protein receptor 5 (TGR5), sphingosine-1-phosphate receptor 2 (S1PR2), and cholinergic receptor muscarinic 2 (CHRM2). All of them are implicated in the development of metabolic and immunological diseases in response to endobiotic and xenobiotic exposure. Because epigenetic regulation is critical for organisms to adapt to constant environmental changes, this review article summarizes epigenetic regulation as well as post-transcriptional modification of bile acid receptors. In addition, the focus of this review is on the liver and digestive tract although these receptors may have effects on other organs. Those regulatory mechanisms are implicated in the disease process and critically important in uncovering innovative strategy for prevention and treatment of metabolic and immunological diseases. Keywords: Bile acid receptor, Farnesoid X receptor (FXR), G protein-coupled bile acid receptor, Takeda G protein receptor 5 (TGR5), Sphingosine-1-phosphate receptor 2 (S1PR2), Acetylation, Methylation, Glycosylation
url http://www.sciencedirect.com/science/article/pii/S2542568418300278
work_keys_str_mv AT yujuiyvonnewan regulationofbileacidreceptoractivity
AT lilisheng regulationofbileacidreceptoractivity
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