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Shear stress modulates expression of Cu/Zn superoxide dismutase in human aortic endothelial cells

  • Nobutaka Inoue
    ,
  • Santhini Ramasamy
    ,
  • Tohru Fukai
    ,
  • Robert M. Nerem
    ,
  • David G. Harrison(corresponding author)
*Corresponding author for this work
  • Emory University
    ,
  • Georgia Institute of Technology
    ,
  • VA Medical Center
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

A major determinant of the level of cellular superoxide anion (O2.) is the disputation of O2. to hydrogen peroxide by the enzyme superoxide dismutase (SOD). Three forms of SOD exist, but in endothelial cells, the major form outside of the mitochondria is the cytosolic copper/zinc- containing superozide dismutase (Cu/Zn SOD). Since fluid shear stress is an important determinant of the function and structure of endothelial cells in vivo, we examined the effect of laminar shear stress on the expression of Cu/Zn SOD in cultured human aortic endothelial cells. Laminar shear stress of 0.6 to 15 dyne/cm2 increased Cu/Zn SOD mRNA in a time- and dose-dependent manner in human aortic endothelial cells. Shear stress also increased both Cu/Zn SOD protection content and the enzyme activity. Nuclear run-on assays showed that nuclei from human aortic endothelial cells exposed to laminar shear stress had a 1.6-fold greater transcriptional activity of the Cu/Zn SOD gene compared with cells not exposed to shear, indicating that an increase in Cu/Zn SOD mRNA induced by laminar shear stress is at least in part mediated by increased transcription. In contrast, shear stress had no effect on Cu/Zn SOD mRNA levels in human aortic smooth muscle cells. These findings show that physiological levels of shear stress increase expression of Cu/Zn SOD in the endothelium. This adaptation to shear stress might augment the effect of locally produced NO. and thereby promote the antiatherogenic and antiinflammatory properties of the endothelial cell.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 32-37 (6 pages)

Journal (Volume, Issue Number)

Circulation research (Volume 79, Issue 1)

Publication milestones

  • Published - 07/1996

Publication status

Published - 07/1996

ISSN

0009-7330

Publication IDs

  • Scopus: 0029890099
  • PubMed: 8925565

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
5.58
SciVal
Author count
5
SciVal
citations
234
SciVal
Paper percentile
98
SciVal
Top percentile
5
Fractional count
1
Fractional count
0.20
Fractional count
4
Fractional count
0.80
Fractional count
1
Fractional count
1

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Citation count
246
Captures
60