Role of intracellular labile iron, ferritin, and antioxidant defence in resistance of chronically adapted Jurkat T cells to hydrogen peroxide

被引:28
作者
Al-Qenaei, Abdullah [1 ]
Yiakouvaki, Anthie [1 ]
Reelfs, Olivier [1 ]
Santambrogio, Paolo [2 ]
Levi, Sonia [2 ,3 ]
Hall, Nick D. [4 ]
Tyrrell, Rex M. [1 ]
Pourzand, Charareh [1 ]
机构
[1] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
[2] Ist Sci San Raffaele, I-20132 Milan, Italy
[3] Univ Vita Salute San Raffaele, Milan, Italy
[4] Bath Inst Rheumat Dis, Bath, Avon, England
基金
英国惠康基金;
关键词
Oxidative stress; Labile iron; Ferritin; Mitochondrial ferritin; Necrosis; Hydrogen peroxide; Desferrioxamine; Lysosomes; Mitochondria; ATP; T cell; OXIDATIVE STRESS; MITOCHONDRIAL FERRITIN; INTRALYSOSOMAL IRON; RESPONSIVE ELEMENT; MESSENGER-RNA; ULTRAVIOLET-A; SKIN CELLS; HELA-CELLS; DAMAGE; CHELATORS;
D O I
10.1016/j.freeradbiomed.2013.12.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
To examine the role of intracellular labile iron pool (LIP), ferritin (Ft), and antioxidant defence in cellular resistance to oxidative stress on chronic adaptation, a new H2O2-resistant Jurkat T cell line "HJ16" was developed by gradual adaptation of parental "J16" cells to high concentrations of H2O2. Compared to J16 cells, HJ16 cells exhibited much higher resistance to H2O2-induced oxidative damage and necrotic cell death (up to 3 mM) and had enhanced antioxidant defence in the form of significantly higher intracellular glutathione and mitochondrial ferritin (FtMt) levels as well as higher glutathioneperoxidase (GPx) activity. In contrast, the level of the Ft H-subunit (FtH) in the H2O2-adapted cell line was found to be 7-fold lower than in the parental J16 cell line. While H2O2 concentrations higher than 0.1 mM fully depleted the glutathione content of J16 cells, in HJ16 cells the same treatments decreased the cellular glutathione content to only half of the original value. In HJ16 cells, H2O2 concentrations higher than 0.1 mM increased the level of FtMt up to 4-fold of their control values but had no effect on the FtMt levels in J16 cells. Furthermore, while the basal cytosolic level of LIP was similar in both cell lines, H2O2 treatment substantially increased the cytosolic LIP levels in J16 but not in HJ16 cells. H2O2 treatment also substantially decreased the FtH levels in J16 cells (up to 70% of the control value). In contrast in HJ16 cells, FtH levels were not affected by H2O2 treatment. These results indicate that chronic adaptation of J16 cells to high concentrations of H2O2 has provoked a series of novel and specific cellular adaptive responses that contribute to higher resistance of HJ16 cells to oxidative damage and cell death. Thee include increased cellular antioxidant defence in the form of highez glutathione and FtMt levels, higher GPx activity, and lower FtH levels. Further adaptive responses include the significantly reduced cellular response to oxidant-mediated glutathione depletion, FtH modulation, and labile iron release and a significant increase in FtMt levels following H2O2 treatment. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:87 / 100
页数:14
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