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Oxalomalate, a competitive inhibitor of NADP(+)-dependent isocitrate dehydrogenase, regulates lipid peroxidation-mediated apoptosis in U937 cells

机译:草酸盐,NADP(+)依赖性异柠檬酸脱氢酶的竞争性抑制剂,调节U937细胞中脂质过氧化介导的细胞凋亡

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摘要

Membrane lipid peroxidation processes yield products that may react with DNA and proteins to cause oxidative modifications. Recently, we demonstrated that the control of cytosolic redox balance and the cellular defense against oxidative damage is one of the primary functions of cytosolic NADP+-dependent isocitrate dehydrogenase (IDPc) through to supply NADPH for antioxidant systems. The protective role of IDPc against lipid peroxidation-mediated apoptosis in U937 cells was investigated in control and cells pre-treated with oxlalomalate, a competitive inhibitor of IDPc. Upon exposure to 2,2-azobis (2-amidinopropane) hydrochloride (AAPH) to U937 cells, which induces lipid peroxidation in membranes, the susceptibility to apoptosis was higher in oxalomalate-treated cells as compared to control cells. The results suggest that IDPc plays an important protective role in apoptosis of U937 cells induced by lipid peroxidation-mediated oxidative stress.
机译:膜脂质过氧化过程产生的产物可能与DNA和蛋白质反应以引起氧化修饰。最近,我们证明了控制细胞质氧化还原平衡和抵抗氧化损伤的细胞防御作用是细胞质NADP +依赖性异柠檬酸脱氢酶(IDPc)的主要功能之一,可为抗氧化系统提供NADPH。在对照和IDPc的竞争性抑制剂草酰草酸酯预处理的细胞中,研究了IDPc对U937细胞中脂质过氧化介导的细胞凋亡的保护作用。暴露于U937细胞的2,2-偶氮双(2-ami基丙烷)盐酸盐(AAPH)会诱导膜中的脂质过氧化,与对照细胞相比,草酰草酸盐处理的细胞对细胞凋亡的敏感性更高。结果表明IDPc在脂质过氧化介导的氧化应激诱导的U937细胞凋亡中起着重要的保护作用。

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