Antioxidant/pro-oxidant equilibrium regulates HIF-1α and NF-κB redox sensitivity -: Evidence for inhibition by glutathione oxidation in alveolar epithelial cells

被引:216
作者
Haddad, JJE
Olver, RE
Land, SC [1 ]
机构
[1] Univ Dundee, Ninewells Hosp & Med Sch, Fac Med,Tayside Inst Child Hlth, Ctr Res Human Dev,Oxygen Signaling Grp, Dundee DD1 9SY, Scotland
[2] Univ Dundee, Ninewells Hosp & Med Sch, Fac Med,Tayside Inst Child Hlth, Ctr Res Human Dev,Lung Membrane Transport Grp, Dundee DD1 9SY, Scotland
关键词
D O I
10.1074/jbc.M000737200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The O-2 and redox-sensitive transcription factors hypoxia inducible factor-1 alpha (HIF-1 alpha) and nuclear factor-kappa B (NF-kappa B) are differentially regulated in the alveolar epithelium over fetal to neonatal oxygen tensions. We have used fetal alveolar type II epithelial cells to monitor their regulation in association with redox responsiveness to antioxidant pretreatment in vitro. N-Acetyl-L-cysteine, a glutathione (GSH) precursor and a potent scavenger of reactive oxygen species, induced HIF-1 alpha and ameliorated NF-kappa B nuclear abundance and DNA binding activity, respectively, in a dose-dependent manner. Analysis of variations in glutathione homeostasis at ascending Delta pO(2) regimen with N-acetyl-(L)-cysteine reveals increased GSH at the expense of the oxidized form of glutathione (GSSG;), thereby shifting GSH/GSSG into reduction equilibrium. Pyrrolidine dithiocarbamate (PDTC), which exerts both antioxidant and pro-oxidant effects, provoked a substantial increase in HIF-1 alpha nuclear abundance, with no apparent effect on its activation. PDTC reduced NF-kappa B nuclear abundance and its inhibitory effects on binding activity are dose-dependent. Assessment of glutathione homeostasis with PDTC shows increasing levels of GSSG at the expense of GSH, lowering GSH/GSSG in favor of an oxidative equilibrium. Our results indicate the hypoxic activation of HIF-1 alpha and the hyperoxic induction of NF-kappa B in the fetal epithelium is redox-sensitive and, thus, tightly regulated by the GSH/GSSG equilibrium. This highlights glutathione as a key regulatory component for determining genetic responsiveness to oxidant/antioxidant imbalance in normal lung development and pathophysiological conditions.
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页码:21130 / 21139
页数:10
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