Interleukin 1beta protects mice from Fas-mediated hepatocyte apoptosis and death

Gastroenterology. 1999 Sep;117(3):661-8. doi: 10.1016/s0016-5085(99)70460-9.

Abstract

Background & aims: Fas-mediated apoptosis is one of the major death processes of hepatocytes in liver diseases. The aim of this study was to determine whether interleukin (IL)-1beta regulates the Fas-mediated apoptotic process of differentiated hepatocytes in vivo.

Methods: IL-1beta was injected into Balb/cA mice 5 hours before lethal challenge with agonistic anti-Fas administration. Survival and hepatocyte apoptotic process of these mice were examined.

Results: IL-1beta pretreatment prolonged animal survival in a dose-dependent manner, and 500 ng of IL-1beta completely protected mice from lethality. Both serum alanine aminotransferase value and hepatic DNA fragmentation were significantly suppressed by IL-1beta pretreatment. IL-1beta affected neither hepatic distribution of anti-Fas antibody nor Fas expression levels on hepatocytes but significantly suppressed Fas-induced activation of hepatic caspase 3-like protease. Suppression of Fas-induced activation of the caspase by IL-1beta was diminished by coadministration with D-galactosamine and reversed by coinjection with an excess amount of uridine.

Conclusions: These results suggest that IL-1beta suppresses Fas-mediated hepatocyte apoptosis by inducing molecule(s) that suppress the apoptosis control machinery upstream of caspase 3. This observation raises the possibility that IL-1beta acts as a negative regulator of Fas-mediated hepatocyte apoptosis during liver injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Apoptosis / drug effects*
  • Apoptosis / physiology
  • Caspase 3
  • Caspases / metabolism
  • Cell Death / drug effects
  • Cell Death / physiology
  • DNA Fragmentation
  • Enzyme Precursors / metabolism
  • Female
  • Flow Cytometry
  • Interleukin-1 / pharmacology*
  • Interleukin-1 / physiology
  • Liver / cytology*
  • Liver / drug effects
  • Liver / metabolism
  • Mice
  • Mice, Inbred BALB C
  • fas Receptor / metabolism

Substances

  • Enzyme Precursors
  • Interleukin-1
  • fas Receptor
  • Alanine Transaminase
  • Casp3 protein, mouse
  • Caspase 3
  • Caspases