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培养细胞中谷胱甘肽过氧化物酶活性对亚硒酸盐补充的反应差异。

Variations among cultured cells in glutathione peroxidase activity in response to selenite supplementation.

作者信息

Sandström B E, Carlsson J, Marklund S L

出版信息

Biochim Biophys Acta. 1987 Jul 6;929(2):148-53. doi: 10.1016/0167-4889(87)90170-4.

Abstract

The aim of this study was to devise conditions for manipulation of the activity of selenium-dependent glutathione peroxidase in cell lines by means of variation in culture medium contents of selenite and fetal calf serum. Nine different cell lines were studied. A low glutathione peroxidase activity was, in most cases, obtained by the use of a medium with a low (2%) serum content. Selenite induced in most of the cell lines an increase in glutathione peroxidase activity, with a plateau ranging from 10 nM to 300-1000 nM. Growth-retarding effects of selenite became apparent at 300-2000 nM, showing a large cell line variation. Supplementation with 50-100 nM selenite for 1 week should generally be suitable for maximal glutathione peroxidase induction. The selenium contents of serum batches were highly variable, pointing to the importance of using only one well-defined, preferably low-selenium, batch. The glutathione peroxidase activities varied considerably between cell lines and the selenite-induced increases ranged from negligible to more than 10-fold. The availability of cell lines with such variable responses should be valuable for experiments aimed at evaluating the importance of glutathione peroxidase and selenium compounds independently of glutathione peroxidase for the protection against oxidative insult.

摘要

本研究的目的是通过改变培养基中硒酸盐和胎牛血清的含量,设计出在细胞系中操纵硒依赖性谷胱甘肽过氧化物酶活性的条件。研究了9种不同的细胞系。在大多数情况下,使用血清含量低(2%)的培养基可获得较低的谷胱甘肽过氧化物酶活性。在大多数细胞系中,亚硒酸盐可诱导谷胱甘肽过氧化物酶活性增加,平台期范围为10 nM至300 - 1000 nM。亚硒酸盐在300 - 2000 nM时生长抑制作用明显,且细胞系差异较大。一般来说,补充50 - 100 nM亚硒酸盐1周应适合最大程度地诱导谷胱甘肽过氧化物酶。血清批次中的硒含量变化很大,这表明仅使用一批明确界定的、最好是低硒的血清的重要性。不同细胞系之间谷胱甘肽过氧化物酶活性差异很大,亚硒酸盐诱导的增加范围从可忽略不计到超过10倍。具有这种可变反应的细胞系对于旨在独立于谷胱甘肽过氧化物酶评估谷胱甘肽过氧化物酶和硒化合物对抵抗氧化损伤重要性的实验应该是有价值的。

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