Involvement of IL-1beta and IL-10 in IFN-alpha-mediated antiviral gene induction in human hepatoma cells

Biochem Biophys Res Commun. 2002 Jun 7;294(2):414-22. doi: 10.1016/S0006-291X(02)00502-8.

Abstract

Crosstalk between interferons (IFNs) and several cytokines is likely to play an important role in viral clearance in chronic hepatitides B and C. We investigated the influence of this phenomenon on IFN-inducible antiviral gene expression in HuH-7 human hepatoma cells. HuH-7 cells were treated with IFN-alpha in the absence or presence of interleukin-1beta (IL-1beta) or IL-10 and the expression of antiviral genes such as 2(')5(')-oligoadenylate synthetase (2(')5(')-OAS) and double-stranded RNA-dependent protein kinase (PKR), as well as activation of signal transducer and activator of transcription 1 (STAT1), a key step for relaying the IFN-alpha signals, was analyzed by Northern blotting, Western blotting, and the reporter gene transfection assay. IL-1beta potentiated IFN-alpha-induced 2(')5(')-OAS and PKR gene expression, similar to expression of the transfected reporter genes containing the IFN-stimulated regulatory elements, while IL-10 suppressed IFN-alpha-stimulated gene expression. With regard to IFN-alpha signaling, IL-1beta enhanced both tyrosine and serine phosphorylation of STAT1 through p38 mitogen-activated protein kinase activation. In contrast, IL-10 inhibited IFN-alpha-mediated tyrosine phosphorylation of STAT1 by induction of a Janus kinase inhibitor, JAB. IL-1beta and IL-10 interact with IFN-alpha to up- and down-regulate antiviral gene expression, respectively, by modulating STAT1 activation induced by IFN-alpha.

MeSH terms

  • 2',5'-Oligoadenylate Synthetase / biosynthesis
  • Blotting, Northern
  • Blotting, Western
  • Carcinoma, Hepatocellular / immunology
  • Carcinoma, Hepatocellular / metabolism*
  • DNA-Binding Proteins / metabolism
  • Gene Expression / drug effects
  • Gene Expression Regulation / drug effects*
  • Gene Expression Regulation / immunology
  • Genes, Reporter
  • Humans
  • Interferon-alpha / metabolism*
  • Interferon-alpha / pharmacology
  • Interleukin-1 / metabolism*
  • Interleukin-1 / pharmacology
  • Interleukin-10 / metabolism*
  • Interleukin-10 / pharmacology
  • Protein Biosynthesis
  • Repressor Proteins*
  • STAT1 Transcription Factor
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Suppressor of Cytokine Signaling 3 Protein
  • Suppressor of Cytokine Signaling Proteins
  • Trans-Activators / metabolism
  • Transcription Factors*
  • Transcriptional Activation
  • Transfection
  • Tumor Cells, Cultured
  • eIF-2 Kinase / biosynthesis

Substances

  • DNA-Binding Proteins
  • Interferon-alpha
  • Interleukin-1
  • Repressor Proteins
  • SOCS3 protein, human
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Suppressor of Cytokine Signaling 3 Protein
  • Suppressor of Cytokine Signaling Proteins
  • Trans-Activators
  • Transcription Factors
  • Interleukin-10
  • eIF-2 Kinase
  • 2',5'-Oligoadenylate Synthetase