自由基诱导HL-60人白血病细胞的粒细胞成熟:涉及羟基自由基的细胞分化假说。

K Nagy, G Pásti, L Bene, I Zs-Nagy
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引用次数: 37

摘要

肿瘤细胞的超氧化物歧化酶(SOD)活性通常低于分化细胞,提示氧自由基参与了细胞成熟过程。已知产生氢氧根的系统的效应。在最佳条件下培养HL-60细胞96小时,检测自由基。羟基自由基由ADP-Fe2+(或ATP-Fe2+)配合物与H2O2的Fenton反应产生。OH引起的变化。比较dmso对HL-60细胞分化的影响。流式细胞术检测细胞数量、活力、胸腺嘧啶掺入、tpa诱导的NBT还原和碘化丙啶染色。哦。生成系统抑制白血病细胞的生长和胸苷结合,其方式取决于H2O2的添加剂量(从0.005到0.05 mM)。此外,越来越多的处理细胞显示出细胞分化的迹象。在dmso处理的细胞中,SOD和过氧化氢酶活性在培养6天后增加。结果表明,部分OH。由超氧化物歧化酶产生的H2O2自由基可能是分化的必要条件,而OH的过量产生则可能是分化的必要条件。导致细胞死亡或老化。我们建议OH。自由基可能在细胞生理学中扮演比仅仅引起氧化损伤更复杂的角色。
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Induction of granulocytic maturation in HL-60 human leukemia cells by free radicals: a hypothesis of cell differentiation involving hydroxyl radicals.

Tumor cells usually contain lower superoxide dismutase (SOD) activity than differentiating cells, suggesting the involvement of oxygen free radicals in cell maturation. The effects of a system known to produce the OH. radicals were tested on HL-60 cells cultured under optimum conditions for 96 hr. Hydroxyl radicals were generated by a Fenton reaction, involving an ADP-Fe2+ (or ATP-Fe2+) complex and H2O2. Changes induced by OH. were compared to the effects of DMSO-induced differentiation of HL-60 cells. Cell numbers, viability, thymidine incorporation, TPA-induced NBT reduction and propidium iodide staining in flow cytometry were determined. The OH. generating system inhibited the growth and thymidine incorporation of leukemic cells in a manner dependent on the dose of added H2O2 (from 0.005 to 0.05 mM). In addition, an increasing proportion of the treated cells displayed signs of cell differentiation. In DMSO-treated cells, SOD and catalase activities increased after 6 days of culturing. The results show that a portion of the OH. free radicals derived from H2O2, produced by the action of SOD, may be a necessary prerequisite for differentiation, whereas an overproduction of OH. causes cell lethality or aging. We suggest that OH. free radicals may have a more complex role in cell physiology than simply causing oxidative damage.

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