Adenovirus genes that modulate the sensitivity of virus-infected cells to lysis by TNF

J Cell Biochem. 1993 Dec;53(4):329-35. doi: 10.1002/jcb.240530410.

Abstract

TNF is a key inflammatory cytokine with antiviral properties. Human adenoviruses encode several intracellular proteins that mediate the effects of TNF. Expression of the adenovirus immediate early E1A proteins induces viral genes and a host of cellular genes, drives G0 cells into S-phase, and induces apoptosis and susceptibility to TNF-induced apoptosis. The adenovirus E1B-19K protein inhibits both E1A- and TNF-induced apoptosis. The E3-14.7K protein and the E3-10.4K/14.5K complex of proteins inhibit TNF- but not E1A-induced apoptosis. The E3 14.7K and 10.4K/14.5K proteins inhibit TNF activation of cytosolic phospholipase A2 (cPLA2), which may explain how they inhibit TNF cytolysis. Since eicosinoids produced from arachidonic acid (the product of cPLA2) are potent mediators of inflammation, the E3 proteins may block the inflammatory response to adenovirus infection. These adenovirus proteins should be novel tools to understand adenovirus pathogenesis, TNF signal transduction, and TNF cytolysis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Adenoviridae / genetics*
  • Adenovirus E1A Proteins / genetics
  • Adenovirus E1A Proteins / pharmacology
  • Adenovirus Early Proteins / genetics*
  • Adenovirus Early Proteins / pharmacology*
  • Apoptosis*
  • Gene Expression
  • Humans
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Adenovirus E1A Proteins
  • Adenovirus Early Proteins
  • Tumor Necrosis Factor-alpha