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Bile Acid-Activated Receptors: GPBAR1 (TGR5) and Other G Protein-Coupled Receptors

  • Verena KeitelEmail author
  • Jan Stindt
  • Dieter Häussinger
Chapter
Part of the Handbook of Experimental Pharmacology book series

Abstract

The BA-responsive GPCRs S1PR2 and TGR5 are almost ubiquitously expressed in human and rodent tissues. In the liver, S1PR2 is expressed in all cell types, while TGR5 is predominately found in non-parenchymal cells. In contrast to S1PR2, which is mainly activated by conjugated bile acids (BAs), all BAs serve as ligands for TGR5 irrespective of their conjugation state and substitution pattern.

Mice with targeted deletion of either S1PR2 or TGR5 are viable and develop no overt phenotype. In liver injury models, S1PR2 exerts pro-inflammatory and pro-fibrotic effects and thus aggravates liver damage, while TGR5 mediates anti-inflammatory, anti-cholestatic, and anti-fibrotic effects. Thus, inhibitors of S1PR2 signaling and agonists for TGR5 have been employed to attenuate liver injury in rodent models for cholestasis, nonalcoholic steatohepatitis, and fibrosis/cirrhosis.

In biliary epithelial cells, both receptors activate a similar signaling cascade resulting in ERK1/2 phosphorylation and cell proliferation. Overexpression of both S1PR2 and TGR5 was found in human cholangiocarcinoma tissue as well as in CCA cell lines, where stimulation of both GPCRs resulted in transactivation of the epidermal growth factor receptor and triggered cell proliferation as well as increased cell migration and invasiveness.

This chapter will focus on the function of S1PR2 and TGR5 in different liver cell types and summarizes current knowledge on the role of these receptors in liver disease models.

Keywords

Bile acid receptor Bile acids G protein-coupled receptor Liver disease S1PR2  TGR5 

Notes

Acknowledgment

Our studies reported herein were supported by DFG through SFB974 “Communication and systems relevance in liver damage and regeneration.”

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© Springer Nature Switzerland AG 2019

Authors and Affiliations

  1. 1.Clinic for Gastroenterology, Hepatology and Infectious DiseasesUniversity Hospital Düsseldorf, Medical Faculty at Heinrich-Heine-UniversityDüsseldorfGermany

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