Goligorsky M S, Morgan M A, Lyubsky S, Gross R W, Adams D T, Spitz D R
Department of Medicine, State University of New York, Stony Brook 11794.
Arch Biochem Biophys. 1993 Feb 15;301(1):119-28. doi: 10.1006/abbi.1993.1123.
Renal epithelial cells resistant to oxidant stress mediated by hydrogen peroxide have been isolated and characterized. African green monkey kidney epithelial cell line, BSC-1 cells, chronically exposed to 50 microM hydrogen peroxide for 15 passages exhibited increased catalase (1.5-fold) and glutathione peroxidase (2.4-fold) activity, as well as increased total cellular glutathione (1.6-fold). This was associated with the acquisition of resistance to hydrogen peroxide cytotoxicity, as judged by nuclear staining with ethidium homodimer and clonogenic survival assay. H2O2-adapted and wild-type BSC-1 cells were used to examine the role of elevated cytosolic calcium concentration and the activation of phospholipase A2 in the development of lethal cell injury. Despite dramatic differences in resistance to oxidative stress, both cell types showed similar kinetics of cytosolic calcium increase in response to challenge with hydrogen peroxide. In contrast to this, oxidant-induced release of arachidonic acid correlated with the resistance of both types of BSC-1 cells to oxidative stress. A mechanism-based inhibitor of calcium-independent phospholipase A2 (Hazen et al., J. Biol. Chem. 266, 7227, 1991) reduced oxidant-induced lethal cell injury, suggesting that this class of phospholipases contributes to damage of BSC-1 cells exposed to hydrogen peroxide. H2O2-adapted BSC-1 cells may represent a valuable tool to study adaptation to oxidative stress and various mechanisms of cell injury.
已分离并鉴定出对过氧化氢介导的氧化应激具有抗性的肾上皮细胞。非洲绿猴肾上皮细胞系BSC - 1细胞,长期暴露于50微摩尔过氧化氢中传代15次后,过氧化氢酶活性增加(1.5倍),谷胱甘肽过氧化物酶活性增加(2.4倍),细胞内总谷胱甘肽也增加(1.6倍)。通过用乙锭同二聚体进行核染色和克隆形成存活试验判断,这与获得对过氧化氢细胞毒性的抗性有关。用适应过氧化氢的和野生型BSC - 1细胞来研究细胞溶质钙浓度升高和磷脂酶A2激活在致死性细胞损伤发生过程中的作用。尽管在对氧化应激的抗性上存在显著差异,但两种细胞类型在受到过氧化氢刺激时,细胞溶质钙增加的动力学表现相似。与此相反,氧化剂诱导的花生四烯酸释放与两种类型的BSC - 1细胞对氧化应激的抗性相关。一种基于机制的非钙依赖性磷脂酶A2抑制剂(Hazen等人,《生物化学杂志》,第266卷,第7227页,1991年)可减轻氧化剂诱导的致死性细胞损伤,这表明这类磷脂酶会导致暴露于过氧化氢的BSC - 1细胞受损。适应过氧化氢的BSC - 1细胞可能是研究氧化应激适应和细胞损伤各种机制的有价值工具。