Novel Nox homologues in the vasculature: focusing on Nox4 and Nox5

被引:85
作者
Montezano, Augusto C. [1 ]
Burger, Dylan [1 ]
Ceravolo, Graziela S. [1 ,2 ]
Yusuf, Hiba [1 ]
Montero, Maria [1 ,3 ]
Touyz, Rhian M. [1 ]
机构
[1] Ottawa Hosp Res Inst, Kidney Res Ctr, Ottawa, ON K1H 8M5, Canada
[2] Univ Sao Paulo, Inst Biomed Sci, Dept Pharmacol, BR-05508900 Sao Paulo, Brazil
[3] Univ Salamanca, Dept Physiol & Pharmacol, Salamanca 37007, Spain
基金
巴西圣保罗研究基金会; 加拿大健康研究院;
关键词
endothelium; hydrogen peroxide; NADPH oxidase (Nox); reactive oxygen species; superoxide; vascular smooth muscle cell; SMOOTH-MUSCLE-CELLS; OXYGEN SPECIES GENERATION; NADPH OXIDASE NOX4; NAD(P)H OXIDASE; ANGIOTENSIN-II; ENDOTHELIAL-CELLS; OXIDATIVE STRESS; UP-REGULATION; INDUCED PROLIFERATION; GP91(PHOX) HOMOLOGS;
D O I
10.1042/CS20100384
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The Noxes (NADPH oxidases) are a family of ROS (reactive oxygen species)-generating enzymes. Of the seven family members, four have been identified as important sources of ROS in the vasculature: Nox1, Nox2, Nox4 and Nox5. Although Nox isoforms can be influenced by the same stimulus and co-localize in cellular compartments, their tissue distribution, subcellular regulation, requirement for cofactors and NADPH oxidase subunits and ability to generate specific ROS differ, which may help to understand the multiplicity of biological functions of these oxidases. Nox4 and Nox5 are the newest isoforms identified in the vasculature. Nox4 is the major isoform expressed in renal cells and appear to produce primarily H2O2. The Nox5 isoform produces ROS in response to increased levels of intracellular Ca2+ and does not require the other NADPH oxidase subunits for its activation. The present review focuses on these unique Noxes, Nox4 and Nox5, and provides novel concepts related to the regulation and interaction in the vasculature, and discusses new potential roles for these isoforms in vascular biology.
引用
收藏
页码:131 / 141
页数:11
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