Lethal hepatitis after gene transfer of IL-4 in the liver is independent of immune responses and dependent on apoptosis of hepatocytes: a rodent model of IL-4-induced hepatitis

J Immunol. 2001 Apr 15;166(8):5225-35. doi: 10.4049/jimmunol.166.8.5225.

Abstract

The putative role of IL-4 in human and animal models of hepatitis has not yet been directly determined. We now report that direct expression of IL-4 in the liver of rats or mice using recombinant adenoviruses coding for rat or mouse IL-4 (AdrIL-4 and AdmIL-4, respectively) results in a lethal, dose-dependent hepatitis. The hepatitis induced by IL-4 was characterized by hepatocyte apoptosis and a massive monocyte/macrophage infiltrate. IL-4-induced hepatitis was independent of T cell-mediated immune responses. Hepatitis occurred even after gene transfer of IL-4 into nude rats, CD8-depleted rats, cyclosporine A-treated rats, or recombinase-activating gene 2(-/-) immunodeficient mice. Peripheral depletion of leukocytes using high doses of cyclophosphamide, and/or the specific depletion of liver macrophages with liposome-encapsulated dichloromethylene diphosphonate in rats did not block lethal IL-4-induced hepatitis. Direct transduction of hepatocytes with adenoviruses was not essential, since injection of AdrIL-4 into the hind limb induced an identical hepatitis. Finally, primary rat hepatocytes in culture also showed apoptosis when cultured in the presence of rIL-4. IL-4-dependent hepatitis was associated with increases in the intrahepatic levels of IFN-gamma, TNF-alpha, and Fas ligand. Administration of AdmIL-4 to IFN-gamma, TNF-alpha receptor type I, or TNF-alpha receptor type II knockout mice also resulted in lethal hepatitis, whereas a moderate protection was observed in Fas-deficient lpr mice. IL-4-dependent hepatocyte apoptosis could be abolished by treatment with caspase inhibitory peptides. Our results thus demonstrate that IL-4 causes hepatocyte apoptosis, which is only partially dependent on the activation of Apo-1-Fas signaling and is largely independent of any immune cells in the liver.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Adenoviridae / genetics
  • Adenoviridae / immunology
  • Amino Acid Chloromethyl Ketones / therapeutic use
  • Animals
  • Apoptosis / drug effects
  • Apoptosis / immunology*
  • Caspase Inhibitors
  • Cell Movement / immunology
  • Cysteine Proteinase Inhibitors / therapeutic use
  • Fas Ligand Protein
  • Gene Transfer Techniques
  • Genetic Vectors / administration & dosage
  • Genetic Vectors / immunology
  • Hepatitis, Viral, Animal / genetics*
  • Hepatitis, Viral, Animal / immunology*
  • Hepatitis, Viral, Animal / mortality
  • Hepatitis, Viral, Animal / pathology
  • Hepatocytes / immunology
  • Hepatocytes / pathology*
  • Immunity, Cellular / genetics
  • Interferon-gamma / biosynthesis
  • Interleukin-4 / administration & dosage*
  • Interleukin-4 / biosynthesis
  • Interleukin-4 / genetics*
  • Interleukin-4 / physiology
  • Kupffer Cells / immunology
  • Kupffer Cells / virology
  • Leukocytes / pathology
  • Liver / drug effects
  • Liver / enzymology
  • Liver / immunology*
  • Liver / pathology
  • Male
  • Membrane Glycoproteins / biosynthesis
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Mice, Knockout
  • Rats
  • Rats, Nude
  • Rats, Wistar
  • T-Lymphocytes / immunology
  • T-Lymphocytes / virology
  • Transduction, Genetic
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Amino Acid Chloromethyl Ketones
  • Caspase Inhibitors
  • Cysteine Proteinase Inhibitors
  • FASLG protein, human
  • Fas Ligand Protein
  • Fasl protein, mouse
  • Faslg protein, rat
  • Membrane Glycoproteins
  • N-acetyl-tyrosyl-valyl-alanyl-aspartyl chloromethyl ketone
  • Tumor Necrosis Factor-alpha
  • Interleukin-4
  • Interferon-gamma