STAT1 plays an essential role in LPS/D-galactosamine-induced liver apoptosis and injury

Am J Physiol Gastrointest Liver Physiol. 2003 Oct;285(4):G761-8. doi: 10.1152/ajpgi.00224.2003. Epub 2003 Jun 19.

Abstract

Interferon-gamma (IFN-gamma) has been implicated in liver damage in animal models and chronic hepatitis C infection; however, the underlying mechanism is not clear. Here we examined the role of STAT1, a key signaling molecule for IFN-gamma, in a model of murine hepatitis induced by the injection of LPS/D-galactosamine and in human hepatoma Hep3B cells. STAT1 is rapidly activated and highly induced after injection of LPS/D-galactosamine. Both overexpression of STAT1 and hepatocellular damage are located in the same pericentral region. Disruption of the STAT1 gene abolishes LPS/D-galactosamine-induced liver injury. Studies from IFN-gamma-deficient mice indicate that IFN-gamma is the major cytokine responsible for activation and hyperexpression of STAT1 in LPS/D-galactosamine-induced hepatitis. Hep3B cells overexpressing dominant negative STAT1 are resistant to IFN-gamma and IFN-gamma + TNF-alpha-induced cell death, whereas Hep3B cells overexpressing wild-type STAT1 are more susceptible to cell death. Taken together, these findings suggest that STAT1 plays an essential role in LPS/D-galactosamine-induced liver apoptosis and injury.

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Cell Line
  • Chemical and Drug Induced Liver Injury* / etiology
  • DNA Fragmentation
  • DNA-Binding Proteins / deficiency
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / physiology*
  • Flow Cytometry
  • Galactosamine / pharmacology*
  • Hepatocytes / chemistry
  • Hepatocytes / ultrastructure
  • Interferon-gamma / deficiency
  • Interferon-gamma / pharmacology
  • Interferon-gamma / physiology
  • Lipopolysaccharides / pharmacology*
  • Liver Diseases / pathology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Phosphorylation
  • Phosphotyrosine / metabolism
  • STAT1 Transcription Factor
  • Trans-Activators / deficiency
  • Trans-Activators / genetics
  • Trans-Activators / physiology*
  • Transfection
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • DNA-Binding Proteins
  • Lipopolysaccharides
  • STAT1 Transcription Factor
  • Stat1 protein, mouse
  • Trans-Activators
  • Tumor Necrosis Factor-alpha
  • Phosphotyrosine
  • Galactosamine
  • Interferon-gamma