Hemin Protects U937 Cells from Oxidative Stress via Glutathione Synthesis

Y. Satoh, Kyohei Oyama, K. Sakurai
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Abstract

Although heme oxygenase-1 and glutathione play important roles in the antioxidant defense system, the sharing and/or cross-talking of the HO-1 and GSH system remain poorly understood. The object of this study is to determine whether the glutathione system is involved in the antioxidant function of hemin. Hydrogen peroxide decreased the viability of the human leukemic monocyte lymphoma cell line U937. When these cells were pretreated with hemin before the addition of hydrogen peroxide, cell death was prevented. An inhibitor of heme oxygenase-1 or glutathione biosynthesis significantly abolished this protective effect of hemin. These results suggest that both heme oxygenase-1 and glutathione are involved in the protective effects of hemin against U937 cell death, which was induced by hydrogen peroxide. Hemin induced an increase in glutathione levels following the upregulation of the gene expression and protein levels of glutamate-cysteine ligase catalytic subunit. The inhibitor of heme oxigenase-1 inhibited the upregulation of glutamate-cysteine ligase catalytic subunit expression. These results suggest that hemin induces glutathione synthesis through heme oxygenase-1 activation to protect cells from hydrogen peroxide-induced oxidative stress.
血红蛋白通过谷胱甘肽合成保护U937细胞免受氧化应激
虽然血红素加氧酶-1和谷胱甘肽在抗氧化防御系统中发挥重要作用,但HO-1和谷胱甘肽系统的共享和/或相互作用仍然知之甚少。本研究的目的是确定谷胱甘肽系统是否参与血红蛋白的抗氧化功能。过氧化氢降低人白血病单核细胞淋巴瘤细胞系U937的活力。当这些细胞在加入过氧化氢之前用血红蛋白预处理时,细胞死亡被阻止。血红素加氧酶-1或谷胱甘肽生物合成抑制剂显著地消除了血红素的这种保护作用。提示血红素加氧酶-1和谷胱甘肽均参与血红素对过氧化氢诱导的U937细胞死亡的保护作用。在谷氨酸-半胱氨酸连接酶催化亚基基因表达和蛋白水平上调后,Hemin诱导谷胱甘肽水平升高。血红素氧化酶-1抑制剂抑制谷氨酸-半胱氨酸连接酶催化亚基表达上调。这些结果表明,血红素通过激活血红素氧化酶-1诱导谷胱甘肽合成,保护细胞免受过氧化氢诱导的氧化应激。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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