Adenovirus E1A and E1B-19K proteins protect human hepatoma cells from transforming growth factor beta1-induced apoptosis

Virus Res. 2010 Jan;147(1):67-76. doi: 10.1016/j.virusres.2009.10.008. Epub 2009 Oct 23.

Abstract

Primary and some transformed hepatocytes undergo apoptosis in response to transforming growth factor beta1 (TGFbeta). We report that infection with species C human adenovirus conferred resistance to TGFbeta-induced apoptosis in human hepatocellular carcinoma cells (Huh-7). Protection against TGFbeta-mediated cell death in adenovirus-infected cells correlated with the maintenance of normal nuclear morphology, lack of pro-caspases 8 and 3 processing, maintenance of the mitochondrial membrane potential, and lack of cellular DNA degradation. The TGFbeta pro-apoptotic signaling pathway was blocked upstream of mitochondria in adenovirus-infected cells. Both the N-terminal sequences of the E1A proteins and the E1B-19K protein were necessary to protect infected cells against TGFbeta-induced apoptosis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenovirus E1A Proteins / physiology*
  • Adenovirus E1B Proteins / physiology*
  • Adenoviruses, Human / immunology*
  • Adenoviruses, Human / pathogenicity*
  • Apoptosis*
  • Cell Line
  • Hepatocytes / virology*
  • Humans
  • Transforming Growth Factor beta1 / immunology*

Substances

  • Adenovirus E1A Proteins
  • Adenovirus E1B Proteins
  • Transforming Growth Factor beta1