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Enhanced γ‐H2AX DNA damage foci detection using multimagnification and extended depth of field in imaging flow cytometry

机译:在成像流式细胞仪中使用多重放大和扩展景深增强了γ-H2AXDNA损伤灶的检测

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摘要

Accurate and rapid methods for the detection of DNA damage foci in eukaryotic cells are central to DNA repair studies, which identify differences in DNA repair capacity in cell lines. Such assays have been important in delineating mechanisms of DNA repair in human cells. Previously we were the first to demonstrate the use of imaging flow cytometry for the detection of γ‐H2AX foci in cells exposed to ionizing radiation causing the induction of DNA strand breaks. In this report we extend these studies and show an enhancement of foci quantitation and image resolution using next generation imaging flow cytometry with the Amnis ImagestreamX Mark II. We demonstrate using cell lines derived from normal individuals, and DNA double strand break repair defective cells that the number of foci observed is significantly increased when using 60× as compared to 40× magnification. Also, foci numbers and resolution is further increased with the application of the focus stacking (Extended Depth of Field–EDF) capacity activated. This report represents the first such demonstration of multimagnification and EDF for the enhanced quantitation of DNA damage in cells and provides a level of resolution, which near matches in situ microscopy methods for the detection of γ‐H2AX foci. © 2015 The Authors. Published by Wiley Periodicals Inc. on behalf of ISAC.
机译:准确快速的检测真核细胞中DNA损伤灶的方法是DNA修复研究的中心,DNA修复研究确定了细胞系中DNA修复能力的差异。这样的测定对于描述人类细胞中DNA修复的机制很重要。以前我们是第一个证明使用成像流式细胞仪检测暴露于电离辐射导致DNA链断裂的细胞中γ-H2AX病灶的方法。在本报告中,我们扩展了这些研究,并显示了使用Amnis Imagestream X Mark II进行的下一代成像流式细胞术可增强病灶定量和图像分辨率。我们证明了使用源自正常个体的细胞系,以及DNA双链断裂修复缺陷细胞,与40x放大倍数相比,使用60x时观察到的病灶数量显着增加。此外,通过激活焦点堆叠(扩展景深–EDF)功能,焦点数量和分辨率会进一步提高。该报告代表了多重放大和EDF的首次此类演示,用于增强细胞中DNA损伤的定量分析,并提供了一定水平的分离度,几乎与用于检测γ-H2AX病灶的原位显微镜方法相匹配。 ©2015作者。由Wiley Periodicals Inc.代表ISAC发布。

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