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Effects of oxidative stress on expression of extracellular superoxide dismutase, CuZn-superoxide dismutase and Mn-superoxide dismutase in human dermal fibroblasts

机译:氧化应激对人皮肤成纤维细胞细胞外超氧化物歧化酶,铜锌超氧化物歧化酶和锰超氧化物歧化酶表达的影响

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pTo determine the effect of oxidative stress on expression of extracellular superoxide dismutase (EC-SOD), CuZn-SOD and Mn-SOD, two fibroblast lines were exposed for periods of up to 4 days to a wide concentration range of oxidizing agents: xanthine oxidase plus hypoxanthine, paraquat, pyrogallol, alpha-naphthoflavone, hydroquinone, catechol, Fe2+ ions, Cu2+ ions, buthionine sulphoximine, diethylmaleate, t-butyl hydroperoxide, cumene hydroperoxide, selenite, citiolone and high oxygen partial pressure. The cell lines were cultured both under serum starvation and at a serum concentration that permitted growth. Under no condition was there any evidence of EC-SOD induction. Instead, the agents uniformly, dose-dependently and continuously reduced EC-SOD expression. We interpret the effect to be due to toxicity. Enhancement of the protection against oxidative stress by addition of CuZn-SOD, catalase and low concentrations of selenite did not influence the expression of any of the SOD isoenzymes. Removal of EC-SOD from cell surfaces by heparin also did not influence SOD expression. Mn-SOD was moderately induced by high doses of the first 11 oxidants. Apart from reduction at high toxic doses, there were no significant effects on the CuZn-SOD activity by any of the treatments. Thus EC-SOD, previously shown to be profoundly influenced by inflammatory cytokines, was not induced by its substrate or other oxidants. In a similar fashion, Mn-SOD, previously shown to be greatly induced and depressed by cytokines, was only moderately influenced by oxidants. We suggest that the regulation of these SOD isoenzymes in mammalian tissues primarily occurs in a manner co-ordinated by cytokines, rather than as a response of individual cells to oxidants./p
机译:>为确定氧化应激对细胞外超氧化物歧化酶(EC-SOD),CuZn-SOD和Mn-SOD表达的影响,将两个成纤维细胞系暴露于宽浓度的氧化剂中长达4天:黄嘌呤氧化酶加次黄嘌呤,百草枯,邻苯三酚,α-萘黄酮,对苯二酚,邻苯二酚,Fe2 +离子,Cu2 +离子,丁硫氨酸亚砜亚胺,马来酸二乙酯,叔丁基氢过氧化物,氢过氧化枯烯,亚硒酸盐,citiolone和高氧分压。在血清饥饿和允许生长的血清浓度下培养细胞系。在任何情况下都没有任何EC-SOD诱导的证据。取而代之的是,这些药剂均匀,剂量依赖性并持续降低EC-SOD表达。我们认为其作用是由于毒性。通过添加CuZn-SOD,过氧化氢酶和低浓度的亚硒酸盐增强对氧化应激的保护作用,不会影响任何SOD同工酶的表达。肝素从细胞表面去除EC-SOD也不影响SOD表达。高剂量的前11种氧化剂可适度诱导Mn-SOD。除了以高毒性剂量还原外,任何一种处理对CuZn-SOD活性均无显着影响。因此,EC-SOD以前被证明受到炎症细胞因子的影响很大,但未被其底物或其他氧化剂诱导。以类似的方式,以前显示出被细胞因子极大地诱导和抑制的Mn-SOD,仅受到氧化剂的中等程度的影响。我们建议哺乳动物组织中这些SOD同工酶的调节主要以细胞因子协调的方式发生,而不是单个细胞对氧化剂的反应。

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