Journal
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
Volume 22, Issue 1, Pages 21-27Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/hq0102.102189
Keywords
neointimal formation; superoxide; NAD(P)H oxidase; balloon injury; nox
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Funding
- NHLBI NIH HHS [HL-58000, HL-66575, HL-38206, HL-58863, HL-57908] Funding Source: Medline
- NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL058863, P01HL058000, R29HL038206, R37HL038206, R01HL066575, R01HL057908, R01HL038206] Funding Source: NIH RePORTER
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Restenosis, a frequent complication of coronary angioplasty, is associated with increased superoxide (O-2.(-)) production. Although the molecular identity of the responsible oxidase is unclear, an NAD(P)H oxidase appears to be involved. In smooth muscle, p22phox and 2 homologues of gp91phox, nox1 and nox4, are expressed, whereas fibroblasts contain gp91phox. To begin investigating the possibility that these oxidase components might contribute to the increased O-2.(-) that accompanies neointimal formation. we measured their expression after balloon injury of the rat carotid artery. The increase in O-2.(-) production 3 to 15 days after surgery was not due to inflammatory cell infiltration but appeared to be derived from medial and neointimal smooth muscle cells and adventitial fibroblasts. Nox1 and p22phox mRNAs were increased 2.7- and 3.6-fold, respectively, at day 3 after injury and remained elevated for 15 days. gp91Phox was increased 7 to 15 days after injury, and nox4 expression was increased 2-fold, but only at day 15 after surgery. These results confirm and extend our previous in vitro data and suggest that in the vasculature, the nox-based NAD(P)H oxidases serve different functions. This dynamic regulation of oxidase components may be critical to smooth muscle phenotypic modulation in restenosis and atherosclerosis.
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