Keyse S M, Tyrrell R M
Swiss Institute for Experimental Cancer Research, Epalinges.
Carcinogenesis. 1990 May;11(5):787-91. doi: 10.1093/carcin/11.5.787.
The induction of heme oxygenase by both hydrogen peroxide and UVA (365 nm) radiation in normal human skin fibroblasts is prevented by prior treatment of cells with the specific iron chelators, o-phenanthroline or desferrioxamine. In addition, both iron chelators protected cells against the lethal effects of H2O2 treatment or UVA irradiation. We propose that the generation of the highly reactive hydroxyl radical by an iron catalyzed Fenton reaction is involved both in the induction of this stress response and, at least in part, in cell killing by the two treatments. These results are also consistent with the idea that the heme oxygenase gene is induced in response to oxidative stress and that its induction may constitute an inducible protective mechanism against oxidative damage induced by both hydrogen peroxide and UVA radiation.
用过氧化氢和UVA(365纳米)辐射诱导正常人皮肤成纤维细胞中的血红素加氧酶,可通过先用特异性铁螯合剂邻菲罗啉或去铁胺处理细胞来阻止。此外,两种铁螯合剂都能保护细胞免受过氧化氢处理或UVA照射的致死效应。我们提出,铁催化的芬顿反应产生的高活性羟基自由基既参与了这种应激反应的诱导,至少部分参与了这两种处理对细胞的杀伤作用。这些结果也与以下观点一致,即血红素加氧酶基因是在氧化应激反应中被诱导的,其诱导可能构成一种针对过氧化氢和UVA辐射诱导的氧化损伤的诱导性保护机制。