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低浓度铅(II)和汞(II)对AS52细胞的诱变作用。

Mutagenesis of AS52 cells by low concentrations of lead(II) and mercury(II).

作者信息

Ariza M E, Williams M V

机构信息

Department of Medical Microbiology and Immunology, Ohio State University, Columbus, USA.

出版信息

Environ Mol Mutagen. 1996;27(1):30-3. doi: 10.1002/(SICI)1098-2280(1996)27:1<30::AID-EM4>3.0.CO;2-I.

Abstract

Little is known at the molecular level concerning the genotoxic effects following the acute exposure of eukaryotic cells to low concentrations of lead (II) or mercury (II). There have been conflicting reports concerning the mutagenic potential of these heavy metals, and there have not been any studies performed to determine the molecular mechanism(s) by which these metals are mutagenic. The Chinese hamster ovary cell line, AS52, contains a stably integrated single functional copy of the Escherichia coli xanthine-guanine phosphoribosyltransferase (gpt) gene. Mutations in the gpt gene confer resistance to 6-thioguanine (TG). There was little effect on viability, as measured by relative cloning efficiency, of AS52 cells exposed to lead (II) or mercury (II) up to concentrations of 0.5 microM and 0.3 microM, respectively. However, higher concentrations of the metals caused a significant increase in cell death. There was also a dose-dependent increase in the isolation of mutants resistant to TG in treated cells when compared to non-treated controls. Concentrations of the metals as low as 0.1 microM caused a significant increase in the number of mutants resistant to TG when compared to the number of spontaneous mutants obtained in nontreated controls. While the molecular mechanism(s) by which lead and mercury (II) are genotoxic is unknown, the results of this study demonstrate that low concentrations of lead (II) and mercury (II) are mutagenic in eukaryotic cells.

摘要

关于真核细胞急性暴露于低浓度铅(II)或汞(II)后的遗传毒性效应,在分子水平上人们了解甚少。关于这些重金属的诱变潜力,一直存在相互矛盾的报道,而且尚未有任何研究来确定这些金属产生诱变作用的分子机制。中国仓鼠卵巢细胞系AS52含有一个稳定整合的大肠杆菌黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(gpt)基因的单功能拷贝。gpt基因中的突变赋予细胞对6 - 硫鸟嘌呤(TG)的抗性。分别将AS52细胞暴露于浓度高达0.5微摩尔/升的铅(II)或0.3微摩尔/升的汞(II),通过相对克隆效率测定,对细胞活力几乎没有影响。然而,更高浓度的这些金属会导致细胞死亡显著增加。与未处理的对照相比,处理后的细胞中对TG有抗性的突变体分离数量也呈剂量依赖性增加。与未处理对照中获得的自发突变体数量相比,低至0.1微摩尔/升的金属浓度就会导致对TG有抗性的突变体数量显著增加。虽然铅和汞(II)产生遗传毒性的分子机制尚不清楚,但本研究结果表明,低浓度的铅(II)和汞(II)在真核细胞中具有诱变作用。

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