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低剂量的溴化乙锭会导致线粒体DNA总量增加,而较高浓度则会在人神经细胞系中诱导线粒体DNA 4997缺失。

A low dose of ethidium bromide leads to an increase of total mitochondrial DNA while higher concentrations induce the mtDNA 4997 deletion in a human neuronal cell line.

作者信息

von Wurmb-Schwark N, Cavelier L, Cortopassi G A

机构信息

Institute of Legal Medicine, Christian-Albrechts-University of Kiel, Arnold-Heller-Str. 12, 24105 Kiel, Germany.

出版信息

Mutat Res. 2006 Apr 11;596(1-2):57-63. doi: 10.1016/j.mrfmmm.2005.12.003. Epub 2006 Feb 20.

Abstract

Ethidium bromide (EtBr) is widely used to deplete mitochondrial DNA (mtDNA) and produce mitochondrial DNA-less cell lines. However, it frequently fails to deplete mtDNA in mouse cells. In this study we show by using a highly sensitive real-time PCR, that low doses of EtBr (10 microM) did lead to a three-fold increase of the total amount of mitochondrial DNA in a human neuronal cell line (Ntera 2). A higher dose of EtBr (25 microM) led to the expected decrease of mtDNA until day 22 when the cells almost died. Cell growth and mtDNA content could be restored after additional 22 days of non-EtBr treatment. The highest concentration of 50 microM also led to a significant increase of mtDNA. The cells died when they had only about 10% of mtDNA left, indicating a mtDNA threshold for cell survival. Additionally, the so-called common 4977 bp deletion could be induced by prolonged exposure to ethidium bromide. Whereas the higher doses led to significant higher amounts of deleted mtDNA.

摘要

溴化乙锭(EtBr)被广泛用于去除线粒体DNA(mtDNA)并产生不含线粒体DNA的细胞系。然而,它在小鼠细胞中常常无法有效去除mtDNA。在本研究中,我们通过使用高灵敏度的实时PCR表明,低剂量的EtBr(10微摩尔)确实导致人神经母细胞瘤细胞系(Ntera 2)中线粒体DNA总量增加了三倍。较高剂量的EtBr(25微摩尔)导致mtDNA如预期那样减少,直到第22天细胞几乎死亡。在额外22天不使用EtBr处理后,细胞生长和mtDNA含量得以恢复。最高浓度50微摩尔也导致mtDNA显著增加。当细胞只剩下约10%的mtDNA时就会死亡,这表明存在细胞存活的mtDNA阈值。此外,长时间暴露于溴化乙锭可诱导所谓的常见4977 bp缺失。而较高剂量导致缺失的mtDNA数量显著增加。

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