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
相关论文
共 50 条
  • [41] Transcriptional regulation of Nox4 by histone deacetylases in human endothelial cells
    Siuda, Daniel
    Zechner, Ulrich
    El Hajj, Nady
    Prawitt, Dirk
    Langer, David
    Xia, Ning
    Horke, Sven
    Pautz, Andrea
    Kleinert, Hartmut
    Foerstermann, Ulrich
    Li, Huige
    BASIC RESEARCH IN CARDIOLOGY, 2012, 107 (05)
  • [42] Upregulation of Nox4 by Hypertrophic Stimuli Promotes Apoptosis and Mitochondrial Dysfunction in Cardiac Myocytes
    Ago, Tetsuro
    Kuroda, Junya
    Pain, Jayashree
    Fu, Cexiong
    Li, Hong
    Sadoshima, Junichi
    CIRCULATION RESEARCH, 2010, 106 (07) : 1253 - U183
  • [43] Endothelial Nox4 NADPH Oxidase Enhances Vasodilatation and Reduces Blood Pressure In Vivo
    Ray, Robin
    Murdoch, Colin E.
    Wang, Minshu
    Santos, Celio X.
    Zhang, Min
    Alom-Ruiz, Sara
    Anilkumar, Narayana
    Ouattara, Alexandre
    Cave, Alison C.
    Walker, Simon J.
    Grieve, David J.
    Charles, Rebecca L.
    Eaton, Philip
    Brewer, Alison C.
    Shah, Ajay M.
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2011, 31 (06) : 1368 - U302
  • [44] Decreased Nox4 levels in the myocardium of patients with aortic valve stenosis
    Moreno, Maria U.
    Gallego, Idoia
    Lopez, Begona
    Gonzalez, Arantxa
    Fortuno, Ana
    San Jose, Gorka
    Valencia, Felix
    Jose Gomez-Doblas, Juan
    de Teresa, Eduardo
    Shah, Ajay M.
    Diez, Javier
    Zalba, Guillermo
    CLINICAL SCIENCE, 2013, 125 (5-6) : 291 - 300
  • [45] The human Nox4: gene, structure, physiological function and pathological significance
    Guo, Shuhui
    Chen, Xiuping
    JOURNAL OF DRUG TARGETING, 2015, 23 (10) : 888 - 896
  • [46] Angiotensin II stimulates superoxide production in the thick ascending limb by activating NOX4
    Massey, Katherine J.
    Hong, Nancy J.
    Garvin, Jeffrey L.
    AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2012, 303 (07): : C781 - C789
  • [47] Nox4 Is a Major Source of Superoxide Production in Human Brain Pericytes
    Kuroda, Junya
    Ago, Tetsuro
    Nishimura, Ataru
    Nakamura, Kuniyuki
    Matsuo, Ryu
    Wakisaka, Yoshinobu
    Kamouchi, Masahiro
    Kitazono, Takanari
    JOURNAL OF VASCULAR RESEARCH, 2014, 51 (06) : 429 - 438
  • [48] Ultrastructural Analysis and Electron Microscopic Localization of Nox4 in Healthy and Atherosclerotic Human Aorta
    Perrotta, Ida
    Sciangula, Alfonso
    Perrotta, Enrico
    Donato, Giuseppe
    Cassese, Mauro
    ULTRASTRUCTURAL PATHOLOGY, 2011, 35 (01) : 1 - 6
  • [49] Tyrosine kinase FYN negatively regulates NOX4 in cardiac remodeling
    Matsushima, Shouji
    Kuroda, Junya
    Zhai, Peiyong
    Liu, Tong
    Ikeda, Shohei
    Nagarajan, Narayani
    Oka, Shin-ichi
    Yokota, Takashi
    Kinugawa, Shintaro
    Hsu, Chiao-Po
    Li, Hong
    Tsutsui, Hiroyuki
    Sadoshima, Junichi
    JOURNAL OF CLINICAL INVESTIGATION, 2016, 126 (09) : 3403 - 3416
  • [50] Involvement of Nox2 and Nox4 NADPH oxidases in early brain injury after subarachnoid hemorrhage
    Zhang, Li
    Li, Zhen
    Feng, Dongxia
    Shen, Haitao
    Tian, Xiaodi
    Li, Haiying
    Wang, Zhong
    Chen, Gang
    FREE RADICAL RESEARCH, 2017, 51 (03) : 316 - 328