Identification of Renox, an NAD(P)H oxidase in kidney

被引:708
作者
Geiszt, M
Kopp, JB
Várnai, P
Leto, TL
机构
[1] NIAID, Host Def Lab, NIH, Bethesda, MD 20892 USA
[2] NIDDKD, Kidney Dis Sect, NIH, Bethesda, MD 20892 USA
[3] NICHHD, Endocrinol & Reprod Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1073/pnas.130135897
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Oxygen sensing is essential for homeostasis in all aerobic organisms, but its mechanism is poorly understood. Data suggest that a phagocytic-like NAD(P)H oxidase producing reactive oxygen species serves as a primary sensor for oxygen. We have characterized a source of superoxide anions in the kidney that we refer to as a renal NAD(P)H oxidase or Renox. Renox is homologous to gp91(phox) (91-kDa subunit of the phagocyte oxidase), the electron-transporting subunit of phagocytic NADPH oxidase. and contains all of the structural motifs considered essential for binding of heme, flavin, and nucleotide, In situ RNA hybridization revealed that renox is highly expressed at the site of erythropoietin production in the renal cortex, showing the greatest accumulation of renox mRNA in proximal convoluted tubule epithelial cells. NIH 3T3 fibroblasts overexpressing transfected Renox show increased production of superoxide and develop signs of cellular senescence. Our data suggest that Renox, as a renal source of reactive oxygen species, is a likely candidate for the oxygen sensor function regulating oxygen-dependent gene expression and may also have a role in the development of inflammatory processes in the kidney.
引用
收藏
页码:8010 / 8014
页数:5
相关论文
共 27 条
[1]   Role of redox potential and reactive oxygen species in stress signaling [J].
Adler, V ;
Yin, ZM ;
Tew, KD ;
Ronai, Z .
ONCOGENE, 1999, 18 (45) :6104-6111
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]   A mammalian H+ channel generated through alternative splicing of the NADPH oxidase homolog NOH-1 [J].
Bánfi, B ;
Maturana, A ;
Jaconi, S ;
Arnaudeau, S ;
Laforge, T ;
Sinha, B ;
Ligeti, E ;
Demaurex, N ;
Krause, KH .
SCIENCE, 2000, 287 (5450) :138-142
[4]  
BAUD L, 1986, AM J PHYSIOL, V251, P765
[5]   Arachidonic acid activates c-jun N-terminal kinase through NADPH oxidase in rabbit proximal tubular epithelial cells [J].
Cui, XL ;
Douglas, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) :3771-3776
[6]   FUNCTIONAL RECONSTITUTION OF THE PHAGOCYTE NADPH OXIDASE BY TRANSFECTION OF ITS MULTIPLE COMPONENTS IN A HETEROLOGOUS SYSTEM [J].
DEMENDEZ, I ;
LETO, TL .
BLOOD, 1995, 85 (04) :1104-1110
[7]   Purification of a novel flavoprotein involved in the thyroid NADPH oxidase -: Cloning of the porcine and human cDNAs [J].
Dupuy, C ;
Ohayon, R ;
Valent, A ;
Noël-Hudson, MS ;
Dème, D ;
Virion, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (52) :37265-37269
[8]  
Ebert BL, 1999, BLOOD, V94, P1864
[9]   Intramembrane bis-heme motif for transmembrane electron transport conserved in a yeast iron reductase and the human NADPH oxidase [J].
Finegold, AA ;
Shatwell, KP ;
Segal, AW ;
Klausner, RD ;
Dancis, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (49) :31021-31024
[10]  
FOX CH, 1993, CURRENT PROTOCOLS IM, V2