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February 9, 2026Journal of Biological Chemistry0 citationsOpen Access

GPR39 mediated molecular signaling by bile acids

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YHYanyun HuangZZZhentao ZiCXChenliang Xia

Key Points

  • The aim is to investigate the molecular signaling mechanisms of GPR39 activated by bile acids.
  • Conducted intracellular calcium measurements in cultured cells
  • Utilized electrophysiologic recordings in Xenopus oocytes
  • Performed Ca<sup>2+</sup> imaging and NanoBiT assays
  • Employed ONE-GO and TANGO techniques for GPR39 validation
  • Analysed kinase phosphorylation in pancreatic and liver tissues
  • Identified specific sulfated bile acids that activate GPR39
  • GPR39 activation involved 9 distinct Gα protein subtypes
  • LCAS induced significant ERK1/2 phosphorylation in pancreas and liver
  • Results were significantly diminished in Gpr39 knockout mice
  • Key residues for GPR39 signaling were established through mutagenesis analysis

Abstract

Bile acids (BAs), long known for roles in food emulsion, also function as biological signals. By measuring intracellular calcium, we have recently discovered that GPR39, a G protein-coupled receptor, is a receptor for 3-O-sulfated BAs including lithocholic acid 3-sulfate (LCAS), taurolithocholic acid 3-sulfate (TLCAS) and glycolithocholic acid 3-sulfate (GLCAS) in cultured cells and in pancreatic acinar cells. We have now used multiple assays from electrophysiologic recording in Xenopus oocytes, Ca2+ imaging, NanoBiT, ONE-GO, to TANGO to validate GPR39 activation by BAs. Among 30 BAs, only sulfated forms (LCAS, TLCAS and GLCAS) evoked GPR39 activation, activating 9 distinct Gα protein subtypes across the Gαq, Gαi, and Gα12/13 subfamilies. LCAS induced phosphorylation of ERK1/2 in the pancreas and the liver, which was markedly attenuated in Gpr39 knockout mice. Mutagenesis analysis identified the key residues essential for GPR39 signaling. Our results have revealed new signaling molecules downstream of GPR39 activation.

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Cite This Study

Huang et al. (2026) studied this question.

synapsesocial.com/papers/698978dff0ec2af6756e7168https://doi.org/10.1016/j.jbc.2026.111241
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