Literature DB >> 18206804

Composition and functions of vascular nicotinamide adenine dinucleotide phosphate oxidases.

Ralf P Brandes1, Katrin Schröder.   

Abstract

Nicotinamide adenine dinucleotide phosphate (NADPH) oxidases are important sources of reactive oxygen species (ROS) and are expressed in at least three different homologues in the vasculature. The enzymes consist of a membrane complex of one of the large catalytically active Nox proteins and p22phox and different cytosolic subunits. Reactive oxygen species formation by the nicotinamide adenine dinucleotide phosphate oxidases Nox1 and Nox2 in arteries is a consequence of an activation of the enzymes by different stimuli such as growth factors, cytokines, and cardiovascular risk factors (cigarette smoke, high blood pressure, oxidized lipids). Nox4, in contrast, is constitutively active, and therefore, ROS formation by this enzyme is controlled on the expression level of the protein. The negative vascular effects of ROS, such as endothelial dysfunction, vascular hypertrophy, aneurysm formation, and inflammatory activation, appear to be the consequence of an activation of Nox1 and Nox2. Nox4, in contrast, potentially elicits positive effects because it promotes differentiation and reduces proliferation of cells. Consequently, selective pharmacologic inhibition of Nox proteins has a potential to interfere with cardiovascular disease initiation and progression.

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Year:  2008        PMID: 18206804     DOI: 10.1016/j.tcm.2007.11.001

Source DB:  PubMed          Journal:  Trends Cardiovasc Med        ISSN: 1050-1738            Impact factor:   6.677


  30 in total

Review 1.  Nox5 and the regulation of cellular function.

Authors:  David J R Fulton
Journal:  Antioxid Redox Signal       Date:  2009-10       Impact factor: 8.401

Review 2.  Reactive oxygen species in phagocytic leukocytes.

Authors:  John M Robinson
Journal:  Histochem Cell Biol       Date:  2008-07-03       Impact factor: 4.304

3.  NADPH oxidase-derived reactive oxygen species contribute to impaired cutaneous microvascular function in chronic kidney disease.

Authors:  Jennifer J DuPont; Meghan G Ramick; William B Farquhar; Raymond R Townsend; David G Edwards
Journal:  Am J Physiol Renal Physiol       Date:  2014-04-23

4.  An oxidized extracellular oxidation-reduction state increases Nox1 expression and proliferation in vascular smooth muscle cells via epidermal growth factor receptor activation.

Authors:  Bojana Stanic; Masato Katsuyama; Francis J Miller
Journal:  Arterioscler Thromb Vasc Biol       Date:  2010-09-02       Impact factor: 8.311

Review 5.  Nox4 and diabetic nephropathy: with a friend like this, who needs enemies?

Authors:  Yves Gorin; Karen Block
Journal:  Free Radic Biol Med       Date:  2013-03-23       Impact factor: 7.376

Review 6.  Nox proteins in signal transduction.

Authors:  David I Brown; Kathy K Griendling
Journal:  Free Radic Biol Med       Date:  2009-07-21       Impact factor: 7.376

7.  LPS-mediated endothelial activation in pulmonary endothelial cells: role of Nox2-dependent IKK-β phosphorylation.

Authors:  Heather Menden; Everett Tate; Neil Hogg; Venkatesh Sampath
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2013-01-18       Impact factor: 5.464

Review 8.  Aiding and abetting roles of NOX oxidases in cellular transformation.

Authors:  Karen Block; Yves Gorin
Journal:  Nat Rev Cancer       Date:  2012-09       Impact factor: 60.716

9.  Endothelial H2O2: a bad guy turning good?

Authors:  Wolfgang F Graier; Markus Hecker
Journal:  Arterioscler Thromb Vasc Biol       Date:  2008-10       Impact factor: 8.311

10.  The NADPH oxidase Nox4 restricts the replicative lifespan of human endothelial cells.

Authors:  Barbara Lener; Rafał Kozieł; Haymo Pircher; Eveline Hütter; Ruth Greussing; Dietmar Herndler-Brandstetter; Martin Hermann; Hermann Unterluggauer; Pidder Jansen-Dürr
Journal:  Biochem J       Date:  2009-10-12       Impact factor: 3.857

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