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Co-visualization of DNA damage and ion traversals in live mammalian cells using a fluorescent nuclear track detector

机译:使用荧光核径迹检测器共同观察活的哺乳动物细胞中DNA损伤和离子穿越的情况

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摘要

The geometric locations of ion traversals in mammalian cells constitute important information in the study of heavy ion-induced biological effect. Single ion traversal through a cellular nucleus produces complex and massive DNA damage at a nanometer level, leading to cell inactivation, mutations and transformation. We present a novel approach that uses a fluorescent nuclear track detector (FNTD) for the simultaneous detection of the geometrical images of ion traversals and DNA damage in single cells using confocal microscopy. HT1080 or HT1080–53BP1-GFP cells were cultured on the surface of a FNTD and exposed to 5.1-MeV neon ions. The positions of the ion traversals were obtained as fluorescent images of a FNTD. Localized DNA damage in cells was identified as fluorescent spots of γ-H2AX or 53BP1-GFP. These track images and images of damaged DNA were obtained in a short time using a confocal laser scanning microscope. The geometrical distribution of DNA damage indicated by fluorescent γ-H2AX spots in fixed cells or fluorescent 53BP1-GFP spots in living cells was found to correlate well with the distribution of the ion traversals. This method will be useful for evaluating the number of ion hits on individual cells, not only for micro-beam but also for random-beam experiments.
机译:离子在哺乳动物细胞中的遍历几何位置是研究重离子诱导的生物效应的重要信息。穿过细胞核的单离子穿越会在纳米水平上产生复杂而庞大的DNA损伤,从而导致细胞失活,突变和转化。我们提出了一种使用荧光核径迹检测器(FNTD)的新方法,用于同时检测共聚焦显微镜检测到的离子穿越和DNA损伤的几何图像。在FNTD的表面培养HT1080或HT1080-53BP1-GFP细胞,并使其暴露于5.1-MeV / n氖离子中。获得离子穿越的位置作为FNTD的荧光图像。将细胞中的局部DNA损伤鉴定为γ-H2AX或53BP1-GFP的荧光斑点。使用共聚焦激光扫描显微镜可以在短时间内获得这些轨迹图像和受损DNA的图像。发现固定细胞中的荧光γ-H2AX斑点或活细胞中的荧光53BP1-GFP斑点指示的DNA损伤的几何分布与离子穿越的分布密切相关。这种方法不仅可用于微束,而且可用于随机束实验,可用于评估单个细胞上的离子命中数。

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