The hepatitis B virus X protein up-regulates tumor necrosis factor alpha gene expression in hepatocytes

Hepatology. 1998 Oct;28(4):1013-21. doi: 10.1002/hep.510280416.

Abstract

Human hepatocytes infected by hepatitis B virus (HBV) produce the proinflammatory cytokine, tumor necrosis factor (TNF-). In this study, we explored the mechanism of induction of TNF- synthesis by HBV. We found that the stable HBV-transfected hepatoma cell line, 2. 2.15, expressed high-molecular-weight (HMW) TNF- mRNAs, which were absent in the parent HepG2 cells. Treatment of 2.2.15 cells with interferon alfa (IFN-) and/or interleukin-1beta (IL-1beta) reduced both viral gene transcription and TNF- mRNA expression. Transient or stable transfection of hepatocyte-derived cell lines with HBV X protein (HBx) expression vectors induced the production of biologically active TNF-. In these cells, the HBx-induced TNF- was detected both as cell-associated and soluble forms. Luciferase gene-expression assays showed that the TNF- gene promoter contained target sequences for HBx trans-activation within the proximal region of the promoter. These results indicate that the hepatocyte TNF- synthesis induced by HBV is transcriptionally up-regulated by HBx. Thus, HBx may have a role in the induction of the intrahepatic inflammatory processes that take place during acute and chronic hepatitis B.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Carcinoma, Hepatocellular
  • Gene Expression Regulation, Neoplastic / drug effects
  • Hepatitis B Antigens / physiology
  • Hepatitis B virus / genetics
  • Hepatitis B virus / physiology*
  • Humans
  • Interferon-alpha / pharmacology
  • Interferon-alpha / physiology
  • Interleukin-1 / pharmacology
  • Interleukin-1 / physiology
  • L Cells
  • Liver Neoplasms
  • Luciferases / biosynthesis
  • Luciferases / genetics
  • Mice
  • Molecular Sequence Data
  • Promoter Regions, Genetic
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Recombinant Fusion Proteins / biosynthesis
  • Trans-Activators / genetics
  • Trans-Activators / physiology*
  • Transcription, Genetic / drug effects
  • Transcriptional Activation
  • Transfection
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / genetics*
  • Viral Regulatory and Accessory Proteins

Substances

  • Hepatitis B Antigens
  • Interferon-alpha
  • Interleukin-1
  • RNA, Messenger
  • Recombinant Fusion Proteins
  • Trans-Activators
  • Tumor Necrosis Factor-alpha
  • Viral Regulatory and Accessory Proteins
  • hepatitis B virus X protein
  • Luciferases