Possible implications of the induction of human heme oxygenase-1 by nitric oxide donors

J Biochem. 1997 Jun;121(6):1162-8. doi: 10.1093/oxfordjournals.jbchem.a021710.

Abstract

To explore the involvement of nitric oxide (NO) in the induction of heme oxygenase-1, an essential enzyme in heme catabolism, we studied the effects of NO donors on the expression of heme oxygenase-1 mRNA in HeLa human cervical cancer cells. Treatment with each of three NO donors, sodium nitroprusside, 3-morpholinosydnonimine, and S-nitroso-L-glutathione, caused noticeable increases in the expression levels of heme oxygenase- mRNA, but not heme oxygenase-2 mRNA. On the other hand, nitrite or 8-bromo cGMP exerted no noticeable effect on the levels of heme oxygenase-1 mRNA. We showed that sodium nitroprusside also increased the levels of heme oxygenase-1 protein. The sodium nitroprusside-mediated increase in heme oxygenase-1 mRNA levels was abolished by treatment with actinomycin D. The expression levels of heme oxygenase-1 mRNA were also increased by NO donors in human melanoma and neuroblastoma cell lines. Thus, the observed induction of heme oxygenase-1 may represent an important response to NO or NO-related oxidative stress. The half lives of heme oxygenase-1 and heme oxygenase-2 mRNAs were estimated to be about 3.2 h and more than 5 h, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Lineage
  • Enzyme Induction
  • HeLa Cells
  • Heme Oxygenase (Decyclizing) / biosynthesis*
  • Heme Oxygenase (Decyclizing) / genetics
  • Heme Oxygenase-1
  • Humans
  • Isoenzymes / biosynthesis
  • Isoenzymes / genetics
  • Membrane Proteins
  • Nitric Oxide / physiology*
  • Tumor Cells, Cultured

Substances

  • Isoenzymes
  • Membrane Proteins
  • Nitric Oxide
  • HMOX1 protein, human
  • Heme Oxygenase (Decyclizing)
  • Heme Oxygenase-1
  • heme oxygenase-2