IRF-1 is an essential mediator in IFN-gamma-induced cell cycle arrest and apoptosis of primary cultured hepatocytes

Biochem Biophys Res Commun. 1999 Apr 21;257(3):672-7. doi: 10.1006/bbrc.1999.0276.

Abstract

IFN-gamma induces cell cycle arrest and p53-independent apoptosis in primary cultured hepatocytes. However, it is not yet understood what molecules regulate the mechanism. We report here that interferon regulatory factor 1 (IRF-1) is an essential molecule in these phenomena. Hepatocytes from IRF-1-deficient mice were completely resistant to IFN-gamma in apoptosis indicated by three different hallmarks such as LDH release, DNA fragmentation and the activation of caspase-3 family. Caspase-1 expression was little detected in hepatocytes, and constitutive and IFN-gamma-induced mRNA expression of Fas or caspase-3 did not change in between wild type and IRF-1-deficient hepatocytes. Expression of IFN-gamma-inducible caspase, caspase-11, did not change either. Thus, it is unlikely that these molecules directly regulate the mechanisms. Interestingly, IRF-1-deficient hepatocytes were also resistant to IFN-gamma-induced cell cycle arrest despite IFN-gamma-induced cell cycle arrest and apoptosis are regulated by independent pathways. Results by Northern blot analysis showed that IFN-gamma-induced but not constitutive p53 mRNA expression was regulated by IRF-1. In fact, IFN-gamma did not induce cell cycle arrest in p53-deficient hepatocytes. Taken together, IRF-1 mediates IFN-gamma signaling into primary hepatocytes for cell cycle arrest via p53 expression and for apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Caspase 3
  • Caspases / genetics
  • Caspases / metabolism
  • Caspases, Initiator
  • Cell Cycle / drug effects
  • Cells, Cultured
  • Coumarins / metabolism
  • DNA Fragmentation / drug effects
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / physiology*
  • Enzyme Activation / drug effects
  • Fas Ligand Protein
  • Female
  • Interferon Regulatory Factor-1
  • Interferon-gamma / pharmacology*
  • L-Lactate Dehydrogenase / metabolism
  • Liver / cytology
  • Liver / drug effects*
  • Liver / metabolism
  • Membrane Glycoproteins / genetics
  • Mice
  • Mice, Inbred C57BL
  • Mutation
  • Oligopeptides / metabolism
  • Phosphoproteins / genetics
  • Phosphoproteins / physiology*
  • RNA, Messenger / metabolism
  • Signal Transduction / drug effects
  • Tumor Suppressor Protein p53 / deficiency
  • Tumor Suppressor Protein p53 / genetics
  • fas Receptor / genetics

Substances

  • Coumarins
  • DNA-Binding Proteins
  • Fas Ligand Protein
  • Fasl protein, mouse
  • Interferon Regulatory Factor-1
  • Irf1 protein, mouse
  • Membrane Glycoproteins
  • Oligopeptides
  • Phosphoproteins
  • RNA, Messenger
  • Tumor Suppressor Protein p53
  • acetyl-aspartyl-glutamyl-valyl-aspartyl-amino-4-methylcoumarin
  • fas Receptor
  • Interferon-gamma
  • L-Lactate Dehydrogenase
  • Casp3 protein, mouse
  • Casp4 protein, mouse
  • Caspase 3
  • Caspases
  • Caspases, Initiator