Upregulation of Nrf2 expression by human cytomegalovirus infection protects host cells from oxidative stress

J Gen Virol. 2013 Jul;94(Pt 7):1658-1668. doi: 10.1099/vir.0.052142-0. Epub 2013 Apr 11.

Abstract

NF-E2 related factor 2 (Nrf2) is a transcription factor that plays a key role(s) in cellular defence against oxidative stress. In this study, we showed that the expression of Nrf2 was upregulated in primary human foreskin fibroblasts (HFFs), following human cytomegalovirus (HCMV/HHV-5) infection. The expression of haem oxygenase-1, a downstream target of Nrf2, was also increased by HCMV infection, and this induction was suppressed in HFFs expressing a small hairpin RNA (shRNA) against Nrf2. The HCMV-mediated increase in Nrf2 expression was abolished when UV-irradiated virus was used or when the activity of casein kinase 2 was inhibited. Host cells infected by HCMV had higher survival rates following oxidative stress induced by buthionine sulfoximine compared with uninfected control cells, but this cell-protective effect was abolished by the use of Nrf2 shRNA. Our results suggest that HCMV-mediated activation of Nrf2 might be beneficial to the virus by increasing the host cell's ability to cope with oxidative stress resulting from viral infection and/or inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Buthionine Sulfoximine / pharmacology
  • Cell Survival
  • Cytomegalovirus / pathogenicity*
  • Cytomegalovirus Infections / virology
  • Cytoprotection
  • Fibroblasts / metabolism
  • Fibroblasts / physiology*
  • Fibroblasts / virology*
  • Heme Oxygenase-1 / genetics
  • Heme Oxygenase-1 / metabolism
  • Humans
  • NF-E2-Related Factor 2 / genetics
  • NF-E2-Related Factor 2 / metabolism*
  • NF-E2-Related Factor 2 / pharmacology
  • Oxidative Stress* / drug effects
  • Up-Regulation*

Substances

  • NF-E2-Related Factor 2
  • NFE2L2 protein, human
  • Buthionine Sulfoximine
  • Heme Oxygenase-1