首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Frequency of CD59 mutations induced in human-hamster hybrid A(L) cells by low-dose X-irradiation.
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Frequency of CD59 mutations induced in human-hamster hybrid A(L) cells by low-dose X-irradiation.

机译:低剂量X射线在人-仓鼠杂种A(L)细胞中诱导CD59突变的频率。

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Determination of the genotoxic effects of ionizing radiation, especially at low-doses, is of great importance for risk assessment, e.g. in radiological diagnostics. The human-hamster hybrid A(L) cell line has been shown previously to be a well-suited in vitro model for the study of mutations induced by various mutagens. The A(L) cells contain a standard set of hamster chromosomes and a single human chromosome 11, which confers the expression of the human cell surface protein CD59. Using CD59 specific antibodies, cells mutated in the CD59 gene can be detected and quantified by the loss of the cell surface marker. In contrast to previous studies, prior to irradiation we removed spontaneous mutants by magnetic cell separation (MACS) which allows analysis of radiation-induced mutation events only. We exposed A(L) cells to 100kV X-rays at 0.1 to 5Gy. The proportions of X-irradiation-induced CD59(-) mutants were quantified by flow cytometry after immunofluorescence labeling. Between 0.2 and 5Gy the yield of CD59 mutants was a linear function of dose. The molecular analysis of individual CD59-negative clones induced after exposure of 1, 3 and 5Gy of X-ray revealed a dose-dependent linear increase of large deletions (>6Mbp), whereas, point mutations could be seen only in spontaneous CD59 mutants or after low-dose exposure (< or =1Gy). We conclude that the modified A(L) assay presented here is appropriate for detection and quantification of non-lethal DNA lesions induced by low-dose ionizing radiation.
机译:确定电离辐射的遗传毒性效应,尤其是在低剂量时,对于风险评估(例如,辐射评估)非常重要。在放射诊断中。先前已证明,人-仓鼠杂种A(L)细胞系是研究各种诱变剂诱导的突变的合适体外模型。 A(L)细胞包含一组标准的仓鼠染色体和一条人类染色体11,这些染色体赋予人类细胞表面蛋白CD59表达。使用CD59特异性抗体,可以通过细胞表面标记的缺失来检测和定量CD59基因中突变的细胞。与以前的研究相反,在辐射之前,我们通过磁性细胞分离(MACS)去除了自发突变体,该突变仅允许分析辐射诱导的突变事件。我们将A(L)细胞暴露于0.1至5Gy的100kV X射线。免疫荧光标记后,通过流式细胞仪定量X射线诱导的CD59(-)突变体的比例。在0.2和5Gy之间,CD59突变体的产量是剂量的线性函数。对X,X,3和5Gy暴露后诱导的单个CD59阴性克隆的分子分析显示,大缺失(> 6Mbp)呈剂量依赖性线性增加,而点突变仅在自发CD59突变体或低剂量暴露(<或= 1Gy)后。我们得出的结论是,此处介绍的改进的A(L)分析适用于检测和定量由低剂量电离辐射诱导的非致死性DNA损伤。

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