TEAD4-mediated upregulation of LPAR3 augments hepatic stellate cell activation in portal hypertension

Cell Biol Toxicol. 2025 Jul 1;41(1):110. doi: 10.1007/s10565-025-10063-1.

Abstract

Based on bioinformatics insights, this study investigates the functions of lysophosphatidic acid receptor 3 (LPAR3) and TEA domain transcription factor 4 (TEAD4) in hepatic stellate cell (HSC) activation and portal hypertension (PHT) progression. LPAR3 exhibited heightened expression in transforming growth factor beta 1-activated human HSCs (LX-2) and in the liver of carbon tetrachloride-challenged mice. Knockdown of LPAR3 alleviated activation and contractile activity of LX-2 cells, as well as ameliorated liver injury and fibrosis in PHT mice, achieved through deactivation of the p38 MAPK and PI3K/AKT signaling. TEAD4, which was enhanced in the activated LX-2 cells and the liver of PHT mice, was identified to bind to the promoter of LPAR3 to promote its transcription. Silencing of TEAD4 similarly inactivated the p38 MAPK and PI3K/AKT pathways by repressing LPAR3, thus alleviating LX-2 cell activation and liver fibrosis in PHT mice. However, these effects were negated by LPAR3 overexpression. In summary, this investigation suggests that TEAD4-mediated upregulation of LPAR3 augments HSC activation and liver fibrosis in PHT by inducing the p38 MAPK and PI3K/AKT axis.

Keywords: LPAR3; P38 MAPK; PI3K/AKT; Portal hypertension; TEAD4.

MeSH terms

  • Animals
  • Carbon Tetrachloride
  • Cell Line
  • DNA-Binding Proteins* / genetics
  • DNA-Binding Proteins* / metabolism
  • Hepatic Stellate Cells* / metabolism
  • Hepatic Stellate Cells* / pathology
  • Humans
  • Hypertension, Portal* / genetics
  • Hypertension, Portal* / metabolism
  • Hypertension, Portal* / pathology
  • Liver / metabolism
  • Liver / pathology
  • Liver Cirrhosis / metabolism
  • Liver Cirrhosis / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Muscle Proteins* / genetics
  • Muscle Proteins* / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Receptors, Lysophosphatidic Acid* / genetics
  • Receptors, Lysophosphatidic Acid* / metabolism
  • Signal Transduction
  • TEA Domain Transcription Factors
  • Transcription Factors* / genetics
  • Transcription Factors* / metabolism
  • Up-Regulation
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • TEA Domain Transcription Factors
  • Transcription Factors
  • Receptors, Lysophosphatidic Acid
  • DNA-Binding Proteins
  • TEAD4 protein, human
  • Muscle Proteins
  • p38 Mitogen-Activated Protein Kinases
  • Proto-Oncogene Proteins c-akt
  • Phosphatidylinositol 3-Kinases
  • Carbon Tetrachloride