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PMID: 10679488 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Transcriptional and posttranscriptional regulation of endothelial nitric oxide synthase expression by hydrogen peroxide.

Circulation research ·Vol. 86 ·No. 3 ·2000-02-18 ·Pages 347-54

Drummond GR, Cai H, Davis ME, Ramasamy S, Harrison DG

Abstract

Diverse stimuli, including shear stress, cyclic strain, oxidized LDL, hyperglycemia, and cell growth, modulate endothelial nitric oxide synthase (eNOS) expression. Although seemingly unrelated, these may all alter cellular redox state, suggesting that reactive oxygen intermediates might modulate eNOS expression. The present study was designed to test this hypothesis. Exposure of bovine aortic endothelial cells for 24 hours to paraquat, a superoxide (O(2)(-*))-generating compound, did not affect eNOS mRNA levels. However, cotreatment with paraquat and either Cu(2+)/Zn(2+) superoxide dismutase or the superoxide dismutase mimetic tetrakis(4-benzoic acid)porphyrin chloride increased eNOS mRNA by 2.3- and 2.2-fold, respectively, implicating a role for H(2)O(2). Direct addition of 100 and 150 micromol/L H(2)O(2) caused increases in bovine aortic endothelial cell eNOS mRNA that were dependent on concentration (ie, 3.1- and 5.2-fold increases) and time, and elevated eNOS protein expression and enzyme activity, accordingly. Nuclear run-on and 5, 6-dichloro-1-beta-D-ribofuranosylbenzimidazole-chase studies showed that H(2)O(2) caused a 3.0-fold increase in eNOS gene transcription and a 2.8-fold increase in eNOS mRNA half-life. Induction of eNOS by H(2)O(2) was not affected by the hydroxyl radical scavenger DMSO, mannitol, or N-tert-butyl-alpha-phenylnitrone, but it was inhibited by the antioxidants N-acetylcysteine, ebselen, and exogenously added catalase. Unlike H(2)O(2), the 4.0-fold induction of eNOS by shear stress (15 dyne/cm(2) for 6 hours) was not inhibited by N-acetylcysteine or exogenous catalase. In conclusion, H(2)O(2) increases eNOS expression through transcriptional and post-transcriptional mechanisms. Although H(2)O(2) does not mediate shear-dependent eNOS regulation, it is likely to be involved in regulation of eNOS expression in response to other physiological and/or pathophysiological stimuli.

MeSH Terms
Animals Cattle Cells, Cultured Enzyme Induction/drug effects Free Radical Scavengers/pharmacology Humans Hydrogen Peroxide/pharmacology Nitric Oxide Synthase/genetics,metabolism Nitric Oxide Synthase Type III Oxidants/pharmacology Paraquat/pharmacology Protein Processing, Post-Translational RNA Stability/drug effects RNA, Messenger/drug effects,metabolism Stress, Mechanical Time Factors Transcription, Genetic/drug effects,physiology
Chemicals
Free Radical Scavengers Oxidants RNA, Messenger Hydrogen Peroxide NOS3 protein, human Nitric Oxide Synthase Nitric Oxide Synthase Type III Paraquat
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Drummond G R
Division of Cardiology, Emory University, Atlanta, GA 30322, USA.
Cai H
Davis M E
Ramasamy S
Harrison D G
Article Info
Journal
Circulation research
Abbr.
Circ Res
ISSN
1524-4571
Published
2000-02-18
Pages
347-54
Language
English
Region
United States
NLM ID
0047103
Subset
IM
Grants
NHLBI NIH HHS · HL390006 · United States
NHLBI NIH HHS · HL58000 · United States
NHLBI NIH HHS · HL59248 · United States
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