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硒代谢物硒代二谷胱甘肽通过一种不同于过氧化氢毒性的机制诱导细胞死亡。

The selenium metabolite selenodiglutathione induces cell death by a mechanism distinct from H2O2 toxicity.

作者信息

Wu L, Lanfear J, Harrison P R

机构信息

Beatson Institute for Cancer Research, CRC Beatson Laboratories, Wolfson Laboratories for Molecular Pathology, Bearsden, Glasgow, UK.

出版信息

Carcinogenesis. 1995 Jul;16(7):1579-84. doi: 10.1093/carcin/16.7.1579.

Abstract

Our previous studies have implicated the selenium metabolite selenodiglutathione (SDG) in the growth inhibitory effects of selenite in vitro. Other work has suggested that reactive oxygen species, the superoxide anion and hydrogen peroxide, may be implicated in selenite toxicity. In this study the mechanism of growth inhibition by SDG and H2O2 has been compared in a mammary cell line, C57. Both SDG and H2O2 had a rapid effect on C57 cells and markedly reduced cloning efficiency within 1 h. However, the mechanisms involved seem to be different, as judged by the following observations: (i) An SDG-resistant cell line (B19) derived from C57 cells is cross-resistant to selenite, but not H2O2; (ii) SDG reduces the levels of the mRNAs for phospholipid hydroperoxide glutathione peroxidase and cytosolic glutathione peroxidase, whereas H2O2 has no effect; (iii) SDG induces both 560 kb and 50 kb DNA fragments, whereas H2O2 only induces 560 kb DNA fragments. This is of interest, since formation of high molecular weight DNA fragments has been recognized as a characteristic of apoptosis.

摘要

我们之前的研究表明,硒代谢产物硒代二谷胱甘肽(SDG)在亚硒酸盐的体外生长抑制作用中发挥作用。其他研究表明,活性氧、超氧阴离子和过氧化氢可能与亚硒酸盐毒性有关。在本研究中,我们比较了SDG和H2O2在乳腺细胞系C57中抑制生长的机制。SDG和H2O2对C57细胞均有快速作用,并在1小时内显著降低克隆效率。然而,从以下观察结果判断,其涉及的机制似乎不同:(i)从C57细胞衍生的SDG抗性细胞系(B19)对亚硒酸盐具有交叉抗性,但对H2O2没有交叉抗性;(ii)SDG降低了磷脂氢过氧化物谷胱甘肽过氧化物酶和胞质谷胱甘肽过氧化物酶的mRNA水平,而H2O2没有影响;(iii)SDG诱导560 kb和50 kb的DNA片段,而H2O2仅诱导560 kb的DNA片段。这一点很有意思,因为高分子量DNA片段的形成已被认为是细胞凋亡的一个特征。

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