The vascular NADPH oxidase subunit p47phox is involved in redox-mediated gene expression
RP Brandes, FJ Miller, S Beer, J Haendeler… - Free Radical Biology …, 2002 - Elsevier
RP Brandes, FJ Miller, S Beer, J Haendeler, J Hoffmann, T Ha, SM Holland, A Görlach…
Free Radical Biology and Medicine, 2002•ElsevierAn NADPH oxidase is thought to be a main source of vascular superoxide (O2−) production.
The functional role of this oxidase, however, and the contribution of the different subunits of
the enzyme to cellular signaling are still incompletely understood. We determined the role of
the p47phox subunit of the oxidase in O2− generation and signaling in aortic rings and
cultured smooth muscle cells (SMC) from wild-type (WT) and p47phox-deficient (p47phox-/-)
mice. Basal O2− levels in aortae of p47phox-/-mice were lower than those in WT aortae …
The functional role of this oxidase, however, and the contribution of the different subunits of
the enzyme to cellular signaling are still incompletely understood. We determined the role of
the p47phox subunit of the oxidase in O2− generation and signaling in aortic rings and
cultured smooth muscle cells (SMC) from wild-type (WT) and p47phox-deficient (p47phox-/-)
mice. Basal O2− levels in aortae of p47phox-/-mice were lower than those in WT aortae …
An NADPH oxidase is thought to be a main source of vascular superoxide (O2−) production. The functional role of this oxidase, however, and the contribution of the different subunits of the enzyme to cellular signaling are still incompletely understood. We determined the role of the p47phox subunit of the oxidase in O2− generation and signaling in aortic rings and cultured smooth muscle cells (SMC) from wild-type (WT) and p47phox-deficient (p47phox -/-) mice. Basal O2− levels in aortae of p47phox -/- mice were lower than those in WT aortae. Infusion of [val5]-angiotensin II increased O2− levels in aortae from WT more than in aortae from p47phox -/- mice. O2− generation was similar in quiescent SMC from WT and p47phox -/- mice. However, exposure to thrombin selectively increased O2− generation in VSMC from WT, but not from p47phox -/- mice. Thrombin-activated redox-mediated signal transduction and gene expression was attenuated in VSMC from p47phox -/- compared to cells from WT mice as determined by p38 MAP kinase activation and VEGF gene expression. We conclude that p47phox is important for vascular ROS production and redox-modulated signaling and gene expression in VSMC.
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