eNOS function is developmentally regulated: Uncoupling of eNOS occurs postnatally

Eugenia Mata-Greenwood, Chrystal Jenkins, Kathryn N. Farrow, G. Ganesh Konduri, James A. Russell, Satyanarayana Lakshminrusimha, Stephen M. Black, Robin H Steinhorn

Research output: Contribution to journalArticle

54 Citations (Scopus)

Abstract

At birth, the transition to gas breathing requires the function of endothelial vasoactive agents. We investigated the function of endothelial nitric oxide synthase (eNOS) in pulmonary artery (PA) vessels and endothelial cells isolated from fetal and young (4-wk) sheep. We found greater relaxations to the NOS activator A-23187 in 4-wk-old compared with fetal vessels and that the NOS inhibitor nitro-L-arginine blocked relaxations in both groups. Relaxations in 4-wk vessels were not blocked by an inhibitor of soluble guanylate cyclase, 1H-[1,2,4]oxadiazolo-[4,3-a]quinoxalin-1-one, but were partially blocked by catalase. We therefore hypothesized that activation of eNOS produced reactive oxygen species in 4-wk but not fetal PA. To address this question, we studied NO and superoxide production by endothelial cells at baseline and following NOS stimulation with A-23187, VEGF, and laminar shear stress. Stimulation of NOS induced phosphorylation at serine 1177, and this event correlated with an increase in NO production in both ages. Upon stimulation of eNOS, fetal PA endothelial cells (PAEC) produced only NO. In contrast 4-wk-old PAEC produced superoxide in addition to NO. Superoxide production was blocked by L-NAME but not by apocynin (an NADPH oxidase inhibitor). L-Arginine increased NO production in both cell types but did not block superoxide production. Heat shock protein 90/eNOS association increased upon stimulation and did not change with developmental age. Cellular levels of total and reduced biopterin were higher in fetal vs. 4-wk cells. Sepiapterin [a tetrahydrobiopterin (BH4) precursor] increased basal and stimulated NO levels and completely blocked superoxide production. We conclude that the normal function of eNOS becomes uncoupled after birth, leading to a developmental adaptation of the pulmonary vascular system to produce oxygen species other than NO. We speculate this may be related to cellular production and/or maintenance of BH4 levels.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Lung Cellular and Molecular Physiology
Volume290
Issue number2
DOIs
StatePublished - Feb 2006
Externally publishedYes

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Nitric Oxide Synthase Type III
Superoxides
Endothelial Cells
Pulmonary Artery
Calcimycin
Arginine
Biopterin
Parturition
HSP90 Heat-Shock Proteins
Quinoxalines
NADPH Oxidase
NG-Nitroarginine Methyl Ester
Catalase
Serine
Vascular Endothelial Growth Factor A
Blood Vessels
Reactive Oxygen Species
Sheep
Respiration
Gases

Keywords

  • Development
  • Endothelial nitric oxide synthase
  • Nitric oxide
  • Pulmonary artery
  • Superoxide

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Cell Biology
  • Physiology

Cite this

eNOS function is developmentally regulated : Uncoupling of eNOS occurs postnatally. / Mata-Greenwood, Eugenia; Jenkins, Chrystal; Farrow, Kathryn N.; Konduri, G. Ganesh; Russell, James A.; Lakshminrusimha, Satyanarayana; Black, Stephen M.; Steinhorn, Robin H.

In: American Journal of Physiology - Lung Cellular and Molecular Physiology, Vol. 290, No. 2, 02.2006.

Research output: Contribution to journalArticle

Mata-Greenwood, Eugenia ; Jenkins, Chrystal ; Farrow, Kathryn N. ; Konduri, G. Ganesh ; Russell, James A. ; Lakshminrusimha, Satyanarayana ; Black, Stephen M. ; Steinhorn, Robin H. / eNOS function is developmentally regulated : Uncoupling of eNOS occurs postnatally. In: American Journal of Physiology - Lung Cellular and Molecular Physiology. 2006 ; Vol. 290, No. 2.
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AU - Russell, James A.

AU - Lakshminrusimha, Satyanarayana

AU - Black, Stephen M.

AU - Steinhorn, Robin H

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