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亚硒酸盐和硒代二谷胱甘肽可抑制AP-1与DNA的结合活性。

AP-1 DNA-binding activity is inhibited by selenite and selenodiglutathione.

作者信息

Spyrou G, Björnstedt M, Kumar S, Holmgren A

机构信息

Medical Nobel Institute for Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.

出版信息

FEBS Lett. 1995 Jul 10;368(1):59-63. doi: 10.1016/0014-5793(95)00599-5.

Abstract

The binding of the transcription factor AP-1 to DNA has been shown to be modulated by redox control mechanisms. Selenite and selenodiglutathione (GS-Se-SG), inhibit mammalian cell growth and are efficient oxidants of reduced thioredoxin and reduced thioredoxin reductase. Here, we report that selenite and GS-Se-SG efficiently inhibited AP-1 DNA-binding in nuclear extracts from 3B6 lymphocytes. A GS-Se-SG concentration of 0.75 microM resulted in 50% inhibition of AP-1 DNA-binding, whereas the same effect was achieved with 7.5 microM selenite. Nuclear extracts prepared from human 3B6 lymphocytes exposed for 4 h to 10 microM selenite showed a 50% reduction of AP-1 binding. These data suggest that selenite and selenodiglutathione inactivate the AP-1 factor and provide a mechanism by which selenium compounds inhibit cell growth.

摘要

转录因子AP-1与DNA的结合已被证明受氧化还原控制机制调节。亚硒酸盐和硒代二谷胱甘肽(GS-Se-SG)可抑制哺乳动物细胞生长,并且是还原型硫氧还蛋白和还原型硫氧还蛋白还原酶的有效氧化剂。在此,我们报告亚硒酸盐和GS-Se-SG可有效抑制3B6淋巴细胞核提取物中AP-1与DNA的结合。0.75微摩尔的GS-Se-SG浓度可导致AP-1与DNA结合受到50%的抑制,而7.5微摩尔的亚硒酸盐可产生相同效果。用10微摩尔亚硒酸盐处理4小时的人3B6淋巴细胞制备的核提取物显示AP-1结合减少了50%。这些数据表明亚硒酸盐和硒代二谷胱甘肽使AP-1因子失活,并提供了一种硒化合物抑制细胞生长的机制。

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