Dengue virus replication in human hepatoma cells activates NF-kappaB which in turn induces apoptotic cell death

J Virol. 1997 Apr;71(4):3244-9. doi: 10.1128/JVI.71.4.3244-3249.1997.

Abstract

The severe outcome of the dengue (DEN) virus infection known as DEN hemorrhagic fever-DEN shock syndrome (DHF-DSS) is, in some cases, accompanied by liver injury. Councilman bodies observed in liver biopsies of DHF-DSS cases may correspond to hepatocytes in apoptosis. We show here that infection of the hepatoma cell line HepG2 with DEN type 1 virus induced cell death typical of apoptosis late in the virus cycle. The transcription factor NF-kappaB was activated concomitantly with viral protein synthesis and thus before the appearance of apoptotic cells. Inhibition of apoptosis was observed when DEN virus-infected cells were treated with NF-kappaB decoys, indicating the involvement of this transcription factor in induction of cell death. Thus, infected hepatocytes appear to be subject to apoptosis in vitro, and this may be a key element in the pathophysiology of hepatic failure associated with DHF-DSS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • Cell Line
  • DNA Fragmentation
  • Dengue Virus / physiology*
  • Humans
  • Liver / cytology
  • NF-kappa B / metabolism*
  • Signal Transduction
  • Tumor Cells, Cultured
  • Virus Replication*

Substances

  • NF-kappa B