Institute for Toxicology and Pharmacology for Natural Scientists, University Hospital Schleswig-Holstein, Campus Kiel, Brunswiker Str. 10, 24105 Kiel, Germany.
Toxicol In Vitro. 2010 Dec;24(8):2090-6. doi: 10.1016/j.tiv.2010.06.005. Epub 2010 Jun 15.
The aim of the present study was to investigate the influence of the maintenance culture conditions on the competence of C6 rat glioma cells to cope with peroxide-induced oxidative stress. C6 cells were maintained either in Ham's nutrient mixture F-10 supplemented with 15% horse serum and 2.5% foetal bovine serum (FBS) or in Dulbecco's Modified Eagle's Medium (DMEM) supplemented with 5% FBS. The differently cultured cells were exposed under identical conditions to hydrogen peroxide (H₂O₂) and cumene hydroperoxide (CHP) in serum-free DMEM. The cells maintained in high serum Ham's F-10 medium (1) were less sensitive towards the cytotoxic action of both peroxides (EC₅₀-values: H₂O₂: 193 ± 23 μM; CHP: 94 ± 16 μM) than the cells maintained in low serum DMEM (EC₅₀-values: H₂O₂: 51 ± 10 μM; CHP: 27 ± 11 μM), (2) eliminated the peroxides (initial concentration: 100 μM) with higher rates (H₂O₂: 56 ± 5.5 vs. 32 ± 2.7, CHP: 32 ± 6 vs. 3.4 ± 0.6 nmol/min mg protein), (3) contained more glutathione (30 ± 2.5 vs. 14 ± 1.1 nmol/mg protein) and (4) owned a higher glutathione peroxidase activity (28 ± 3.4 vs. 9.5 ± 0.8 mU/mg protein). Glutathione reductase and catalase activities were not affected. These results demonstrate that the preceding culture conditions have a lasting effect on the susceptibility of cultured cells to oxidative stressors like peroxides. As cause for these differences a dissimilar supply of the cells with serum born antioxidants like selenium and α-tocopherol is discussed.
本研究的目的是探讨维持培养条件对 C6 大鼠神经胶质瘤细胞应对过氧化诱导的氧化应激能力的影响。C6 细胞分别在添加 15%马血清和 2.5%胎牛血清(FBS)的 Ham's 营养混合物 F-10 或添加 5%FBS 的 Dulbecco's Modified Eagle's Medium (DMEM)中维持培养。在无血清 DMEM 中,以相同条件使不同培养的细胞暴露于过氧化氢(H₂O₂)和过氧化枯烯(CHP)下。在高血清 Ham's F-10 培养基中维持的细胞(1)对两种过氧化物(H₂O₂:193±23 μM;CHP:94±16 μM)的细胞毒性作用的敏感性低于在低血清 DMEM 中维持的细胞(H₂O₂:51±10 μM;CHP:27±11 μM),(2)以更高的速率消除过氧化物(初始浓度:100 μM)(H₂O₂:56±5.5 与 32±2.7,CHP:32±6 与 3.4±0.6 nmol/min mg protein),(3)含有更多的谷胱甘肽(30±2.5 与 14±1.1 nmol/mg protein)和(4)具有更高的谷胱甘肽过氧化物酶活性(28±3.4 与 9.5±0.8 mU/mg protein)。谷胱甘肽还原酶和过氧化氢酶活性不受影响。这些结果表明,先前的培养条件对培养细胞对过氧化物等氧化应激物的敏感性具有持久的影响。作为这些差异的原因,讨论了细胞对血清中抗氧化剂(如硒和α-生育酚)供应的差异。