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An Automated Single Cell Quantitative Imaging Microscopy Approach to Assess Micronucleus Formation Genotoxicity and Chromosome Instability

机译:一种自动化的单细胞定量成像显微镜方法用于评估微核的形成遗传毒性和染色体不稳定

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摘要

Micronuclei are small, extranuclear bodies that are distinct from the primary cell nucleus. Micronucleus formation is an aberrant event that suggests a history of genotoxic stress or chromosome mis-segregation events. Accordingly, assays evaluating micronucleus formation serve as useful tools within the fields of toxicology and oncology. Here, we describe a novel micronucleus formation assay that utilizes a high-throughput imaging platform and automated image analysis software for accurate detection and rapid quantification of micronuclei at the single cell level. We show that our image analysis parameters are capable of identifying dose-dependent increases in micronucleus formation within three distinct cell lines following treatment with two established genotoxic agents, etoposide or bleomycin. We further show that this assay detects micronuclei induced through silencing of the established chromosome instability gene, . Thus, the micronucleus formation assay described here is a versatile and efficient alternative to more laborious cytological approaches, and greatly increases throughput, which will be particularly beneficial for large-scale chemical or genetic screens.
机译:微核是与初级细胞核不同的小的核外小体。微核的形成是一个异常事件,表明存在遗传毒性应激或染色体错误分离事件的历史。因此,评价微核形成的测定法是毒理学和肿瘤学领域中的有用工具。在这里,我们描述了一种新型的微核形成测定法,该测定法利用高通量成像平台和自动图像分析软件在单个细胞水平上对微核进行准确检测和快速定量。我们表明,我们的图像分析参数能够确定两种不同的遗传毒性剂(依托泊苷或博来霉素)治疗后三种不同细胞系中微核形成的剂量依赖性增加。我们进一步表明,该测定法检测通过沉默已建立的染色体不稳定性基因诱导的微核。因此,此处描述的微核形成分析是一种更省力的细胞学方法的通用且有效的替代方法,并且极大地提高了通量,这对于大规模化学或基因筛选特别有利。

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