Involvement of 26-kDa cell-associated TNF-alpha in experimental hepatitis and exacerbation of liver injury with a matrix metalloproteinase inhibitor

J Immunol. 1997 Jan 1;158(1):414-9.

Abstract

TNF-alpha is a pleiotropic cytokine that exists both as a 26-kDa cell-associated and a 17-kDa soluble form. Recently, a class of matrix metalloproteinase inhibitors has been identified that can prevent the processing by TNF convertase of 26-kDa TNF-alpha to its 17-kDa form and can reduce mortality from normally lethal doses of D-galactosamine plus LPS (D-GalN/LPS). Here we report that a matrix metalloproteinase inhibitor, GM-6001, improves survival but does not protect against liver injury from D-GalN/LPS-induced shock in the mouse. In Con A-induced hepatitis, GM-6001 actually exacerbates hepatocellular necrosis and apoptosis despite greater than 90% reduction in plasma TNF-alpha concentrations. Treatment with GM-6001 also has minimal effect on the concentration of membrane-associated TNF-alpha in the livers of animals with Con A induced hepatitis. In contrast, a TNF binding protein (TNF-bp), which neutralizes both membrane-associated and soluble TNF-alpha, prevents D-GalN/LPS- and Con A-induced hepatitis. Our studies suggest that cell-associated TNF-alpha plays a role in the hepatocellular necrosis and apoptosis that accompany D-GalN/LPS- or Con A-induced hepatitis, and that matrix metalloproteinase inhibitors are ineffective in preventing this hepatic injury.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Chemical and Drug Induced Liver Injury / drug therapy
  • Chemical and Drug Induced Liver Injury / mortality
  • Chemical and Drug Induced Liver Injury / pathology*
  • Concanavalin A / toxicity
  • Dipeptides / toxicity*
  • Drug Synergism
  • Galactosamine / chemistry
  • Galactosamine / toxicity
  • Lipopolysaccharides / toxicity
  • Liver / drug effects
  • Liver / injuries
  • Metalloendopeptidases / antagonists & inhibitors*
  • Mice
  • Mice, Inbred C57BL
  • Protease Inhibitors / toxicity*
  • Receptors, Tumor Necrosis Factor / blood
  • Tumor Necrosis Factor-alpha / analysis
  • Tumor Necrosis Factor-alpha / chemistry*
  • Tumor Necrosis Factor-alpha / toxicity*

Substances

  • Dipeptides
  • Lipopolysaccharides
  • N-(2(R)-2-(hydroxamidocarbonylmethyl)-4-methylpentanoyl)-L-tryptophan methylamide
  • Protease Inhibitors
  • Receptors, Tumor Necrosis Factor
  • Tumor Necrosis Factor-alpha
  • Concanavalin A
  • Galactosamine
  • Metalloendopeptidases