期刊
FREE RADICAL BIOLOGY AND MEDICINE
卷 37, 期 10, 页码 1542-1549出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2004.08.011
关键词
NAD(P)H oxidase; Nox; vascular smooth muscle; p22phox; superoxide; reactive oxygen species; free radicals
资金
- NHLBI NIH HHS [HL38206, HL58000] Funding Source: Medline
- NIAMS NIH HHS [AR42426] Funding Source: Medline
The vascular NAD(P)H oxidases constitute important sources of ROS in the vessel wall and have been implicated in vascular disease. Vascular smooth muscle cells (VSMCs) from conduit arteries express two gp91phox homologs, Nox1 and Nox4, of which Nox1 is agonist-sensitive. Because p22phox has been shown to be functionally important in vascular cells stimulated with vasoactive hormones, the relationship of Nox1 and p22phox was investigated in VSMCs from rat and human aortas. Coimmunoprecipitation studies demonstrated that p22phox and hemagglutinin-tagged Nox1 associate in unstimulated VSMCs. These findings were confirmed by confocal microscopy, showing colocalization of the two proteins in their native states in the plasma membrane and submembrane areas of the cell. NADPH-driven superoxide production, as measured by electron spin resonance using 1-hydroxy-3-carboxypyrrolidine as a spin probe, is dependent on the coexpression of both subunits, suggesting the importance of the association for the functional integrity of the enzyme. These results indicate that in contrast to the neutrophil enzyme, VSMCs can use Nox1 rather than gp91phox as a catalytic center in the p22phox-based oxidase and that these two proteins are preassembled at or near the plasma membrane and submembrane vesicular structures in unstimulated cells. (C) 2004 Elsevier Inc. All rights reserved.
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