Literature DB >> 24878541

Bile acid signaling and liver regeneration.

Mingjie Fan1, Xichun Wang2, Ganyu Xu2, Qingfeng Yan1, Wendong Huang3.   

Abstract

The liver is able to regenerate itself in response to partial hepatectomy or liver injury. This is accomplished by a complex network of different cell types and signals both inside and outside the liver. Bile acids (BAs) are recently identified as liver-specific metabolic signals and promote liver regeneration by activating their receptors: Farnesoid X Receptor (FXR) and G-protein-coupled BA receptor 1 (GPBAR1, or TGR5). FXR is a member of the nuclear hormone receptor superfamily of ligand-activated transcription factors. FXR promotes liver regeneration after 70% partial hepatectomy (PHx) or liver injury. Moreover, activation of FXR is able to alleviate age-related liver regeneration defects. Both liver- and intestine-FXR are activated by BAs after liver resection or injury and promote liver regeneration through distinct mechanism. TGR5 is a membrane-bound BA receptor and it is also activated during liver regeneration. TGR5 regulates BA hydrophobicity and stimulates BA excretion in urine during liver regeneration. BA signaling thus represents a novel metabolic pathway during liver regeneration. This article is part of a Special Issue entitled: Nuclear receptors in animal development.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Bile acid; FGF15; FXR; Liver regeneration; TGR5

Mesh:

Substances:

Year:  2014        PMID: 24878541      PMCID: PMC4246016          DOI: 10.1016/j.bbagrm.2014.05.021

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  78 in total

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  29 in total

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Review 6.  Regulation of hepatocyte identity and quiescence.

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7.  Bile acid signaling and bariatric surgery.

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