Adiponectin inhibits steatotic CD95/Fas up-regulation by hepatocytes: therapeutic implications for hepatitis C

J Hepatol. 2009 Jan;50(1):140-9. doi: 10.1016/j.jhep.2008.08.023. Epub 2008 Nov 7.

Abstract

Background/aims: Steatosis may trigger hepatocytes to up-regulate CD95/Fas thereby increasing susceptibility to apoptosis, inflammation and fibrosis. We investigated this concept and potential roles of adiponectin and its receptors (AdipoR1; AdipoR2) in chronically HCV-infected patients.

Methods: In 98 HCV+ patients and 20 controls, sera were tested for HCV genotypes, FFAs, adiponectin and the M30 apoptosis indicator, and biopsies were evaluated for steatosis/inflammation/fibrosis, CD95/Fas (mRNA/protein), adiponectin (mRNA/protein), AdipoR1/-R2 (mRNA) and M30 (protein). We also questioned whether adiponectin protects HepG2 hepatoblastoma cells from FFA-triggered CD95/Fas up-regulation and apoptosis.

Results: Patients [HCV clades 1 (78%), 2 (3%) and 3 (19%)] revealed increased FFA and adiponectin serum levels (p = .005). Hepatocyte CD95/Fas up-regulation correlated with steatosis, inflammation and fibrosis (p = .004). Advanced fibrosis correlated significantly (p = .05) with serum M30. Liver adiponectin correlated with steatosis (p = .016), CD95/Fas (p < .001) and inflammation/fibrosis. Hepatocyte AdipoR2 mRNA specifically correlated with serum adiponectin and steatosis (p = .003), while hepatocyte AdipoR1 mRNA dropped in pronounced fibrosis (p = .060). Finally, adiponectin protected HepG2 cells from FFA-triggered CD95/Fas expression and induction of apoptosis (p = .0396).

Conclusions: In chronic HCV infection, steatosis up-regulates hepatocyte CD95/Fas and thus increases apoptosis, which facilitates inflammation and fibrosis. The physiologic countermeasure of adiponectin up-regulation may offer clues for future therapeutic intervention.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin / metabolism*
  • Adult
  • Aged
  • Aged, 80 and over
  • Apoptosis
  • Case-Control Studies
  • Cell Line, Tumor
  • Fatty Acids, Nonesterified / blood
  • Fatty Liver / metabolism*
  • Fatty Liver / pathology
  • Female
  • Genotype
  • Hepacivirus / genetics
  • Hepatitis C / drug therapy
  • Hepatitis C / metabolism*
  • Hepatitis C / pathology
  • Hepatoblastoma / metabolism
  • Hepatoblastoma / pathology
  • Hepatocytes / metabolism*
  • Hepatocytes / pathology
  • Humans
  • Liver Cirrhosis / metabolism
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / pathology
  • Male
  • Middle Aged
  • Receptors, Adiponectin / metabolism
  • Up-Regulation / physiology*
  • fas Receptor / antagonists & inhibitors*
  • fas Receptor / metabolism

Substances

  • ADIPOR2 protein, human
  • Adiponectin
  • Fatty Acids, Nonesterified
  • Receptors, Adiponectin
  • fas Receptor