Hepatocyte CD36 protects mice from NASH diet-induced liver injury and fibrosis via blocking N1ICD production

Biochim Biophys Acta Mol Basis Dis. 2023 Oct;1869(7):166800. doi: 10.1016/j.bbadis.2023.166800. Epub 2023 Jul 7.

Abstract

Background & aims: Fatty acid translocase CD36 (CD36/FAT) is a widely expressed membrane protein with multiple immuno-metabolic functions. Genetic CD36 deficiency is associated with increased risk of metabolic dysfunction-associated fatty liver disease (MAFLD) in patients. Liver fibrosis severity mainly affects the prognosis in patients with MAFLD, but the role of hepatocyte CD36 in liver fibrosis of MAFLD remains unclear.

Methods: A high-fat high-cholesterol diet and a high-fat diet with high-fructose drinking water were used to induce nonalcoholic steatohepatitis (NASH) in hepatocyte-specific CD36 knockout (CD36LKO) and CD36flox/flox (LWT) mice. Human hepG2 cell line was used to investigate the role of CD36 in regulating Notch pathway in vitro.

Results: Compared to LWT mice, CD36LKO mice were susceptible to NASH diet-induced liver injury and fibrosis. The analysis of RNA-sequencing data revealed that Notch pathway was activated in CD36LKO mice. LY3039478, an inhibitor of γ-secretase, inhibited Notch1 protein S3 cleavage and Notch1 intracellular domain (N1ICD) production, alleviating liver injury and fibrosis in CD36LKO mice livers. Likewise, both LY3039478 and knockdown of Notch1 inhibited the CD36KO-induced increase of N1ICD production, causing the decrease of fibrogenic markers in CD36KO HepG2 cells. Mechanistically, CD36 formed a complex with Notch1 and γ-secretase in lipid rafts, and hence CD36 anchored Notch1 in lipid rafts domains and blocked Notch1/γ-secretase interaction, inhibiting γ-secretase-mediated cleavage of Notch1 and the production of N1ICD.

Conclusions: Hepatocyte CD36 plays a key role in protecting mice from diet-induced liver injury and fibrosis, which may provide a potential therapeutic strategy for preventing liver fibrogenesis in MAFLD.

Keywords: CD36; Fibrosis; Lipid rafts; Notch1; γ-Secretase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid Precursor Protein Secretases / antagonists & inhibitors
  • Animals
  • CD36 Antigens* / deficiency
  • CD36 Antigens* / genetics
  • CD36 Antigens* / metabolism
  • Diet* / adverse effects
  • Gene Deletion
  • Hep G2 Cells
  • Hepatocytes* / metabolism
  • Humans
  • Liver Cirrhosis* / etiology
  • Liver Cirrhosis* / genetics
  • Liver Cirrhosis* / prevention & control
  • Membrane Microdomains
  • Mice
  • Non-alcoholic Fatty Liver Disease* / etiology
  • Non-alcoholic Fatty Liver Disease* / genetics
  • Non-alcoholic Fatty Liver Disease* / prevention & control
  • Peptide Fragments* / antagonists & inhibitors
  • Peptide Fragments* / chemistry
  • Peptide Fragments* / metabolism
  • Phenotype
  • Receptor, Notch1* / chemistry
  • Receptor, Notch1* / metabolism
  • Signal Transduction

Substances

  • Amyloid Precursor Protein Secretases
  • CD36 Antigens
  • Cd36 protein, mouse
  • crenigacestat
  • Notch1 protein, mouse
  • Peptide Fragments
  • Receptor, Notch1