Composition and functions of vascular nicotinamide adenine dinucleotide phosphate oxidases

被引:53
作者
Brandes, Ralf P. [1 ]
Schroeder, Katrin [1 ]
机构
[1] Univ Frankfurt, Inst Kardiovasc Physiol, D-60596 Frankfurt, Germany
关键词
D O I
10.1016/j.tcm.2007.11.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 Nox1and 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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收藏
页码:15 / 19
页数:5
相关论文
共 45 条
[1]   Nox4 as the major catalytic component of an endothelial NAD(P)H oxidase [J].
Ago, T ;
Kitazono, T ;
Ooboshi, H ;
Iyama, T ;
Han, YH ;
Takada, J ;
Wakisaka, M ;
Ibayashi, S ;
Utsumi, H ;
Iida, M .
CIRCULATION, 2004, 109 (02) :227-233
[2]   Endothelial NADPH oxidase as the source of oxidants in lungs exposed to ischemia or high K+ [J].
Al-Mehdi, AB ;
Zhao, GC ;
Dodia, C ;
Tozawa, K ;
Costa, K ;
Muzykantov, V ;
Ross, C ;
Blecha, F ;
Dinauer, M ;
Fisher, AB .
CIRCULATION RESEARCH, 1998, 83 (07) :730-737
[3]   Noxal is a central component of the smooth muscle NADPH oxidase in mice [J].
Ambasta, Rashmi K. ;
Schreiber, Judith G. ;
Janiszewski, Mariano ;
Busse, Rudi ;
Brandes, Ralf P. .
FREE RADICAL BIOLOGY AND MEDICINE, 2006, 41 (02) :193-201
[4]   Direct interaction of the novel nox proteins with p22phox is required for the formation of a functionally active NADPH oxidase [J].
Ambasta, RK ;
Kumar, P ;
Griendling, KK ;
Schmidt, HHHW ;
Busse, R ;
Brandes, RP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (44) :45935-45941
[5]   The NOX family of ROS-generating NADPH oxidases: Physiology and pathophysiology [J].
Bedard, Karen ;
Krause, Karl-Heinz .
PHYSIOLOGICAL REVIEWS, 2007, 87 (01) :245-313
[6]   NOX5 variants are functionally active in endothelial cells [J].
BelAiba, Rachida S. ;
Djordjevic, Talija ;
Petry, Andreas ;
Diemer, Kerstin ;
Bonello, Steve ;
Banfi, Botond ;
Hess, John ;
Pogrebniak, Alexej ;
Bickel, Christian ;
Goerlach, Agnes .
FREE RADICAL BIOLOGY AND MEDICINE, 2007, 42 (04) :446-459
[7]   gp91phox Contributes to NADPH oxidase activity in aortic fibroblasts but not smooth muscle cells [J].
Chamseddine, AH ;
Miller, FJ .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 285 (06) :H2284-H2289
[8]  
Chen H. Q., 2004, Innovative Food Science & Emerging Technologies, V5, P269, DOI 10.1016/j.ifset.2004.03.002
[9]   Nox4 is required for maintenance of the differentiated vascular smooth muscle cell phenotype [J].
Clempus, Roza E. ;
Sorescu, Dan ;
Dikalova, Anna E. ;
Pounkova, Lily ;
Jo, Patricia ;
Sorescu, George P. ;
Lassegue, Bernard ;
Griendling, Kathy K. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2007, 27 (01) :42-48
[10]   H2O2 activates Nox4 through PLA2-dependent arachidonic acid production in adult cardiac fibroblasts [J].
Colston, JT ;
de la Rosa, SD ;
Strader, JR ;
Anderson, MA ;
Freeman, GL .
FEBS LETTERS, 2005, 579 (11) :2533-2540