Journal
CARDIOVASCULAR RESEARCH
Volume 63, Issue 2, Pages 323-330Publisher
OXFORD UNIV PRESS
DOI: 10.1016/j.cardiores.2004.03.018
Keywords
NADPH oxidase; human endothelial cells; anoxia/reoxygenation; E-selectin; NF kappa B; apocynin
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Objective: Anoxia followed by reoxygenation (A/R) increases endothelial cell superoxide (O-2(-)) generation which is implicated in E-selectin overexpression. The mechanisms which govern these processes are not fully understood and therefore the goal of our study was to determine the functional importance of NADPH oxidase in the regulation of E-selectin expression in human umbilical veins endothelial cells (HUVECs) submitted to A/R. Methods: O-2(-) production was estimated using lucigenin chemiluminescence and formazan accumulation. NADPH oxidase expression in HUVECs was studied by RT-PCR and Western blot and E-selectin by Northern blot analysis. NFkappaB activation was assessed by electrophoretic mobility shift assay. Results: A/R caused an increased O-2(-) production which was inhibited by the superoxide dismutase mimetic M40403 (50 mumol/l), the protein kinase C inhibitor chelerythrine (10 mumol/l), the NADPH oxidase inhibitor diphenyleneiodonium (DPI, 10 mumol/l) and the NADPH oxidase assembly blocker apocynin (600 mumol/l). At the end of the anoxic period, the mRNA expression and the protein p47(phox) was increased as compared to normoxic HUVECs. NFkappaB activation of anoxic HUVECs was maximal after 1 h of reoxygenation and returned to basal non-noxic levels after 2 h of reoxygenation. Apocynin reduced the NFkappaB activation at 1 h of reoxygenation. E-selectin mRNA expression was increased after 3 h of reoxygenation of anoxic HUVECs and the SOD mimetic M40403 as well as apocynin prevented this overexpression. Conclusions: Activated NADPH oxidase is a critical enzyme in E-selectin overexpression after A/R of HUVECs. Moreover, A/R increased expression of membranous and cytosolic NADPH oxidase subunits as well as the protein p47(phox). Strategies aimed at preventing endothelial NADPH oxidase activation and/or activity may be useful in controlling leukocyte adhesion during ischemia/reperfusion. (C) 2004 European Society of Cardiology. Elsevier B.V. All rights reserved.
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