Bekeschus Sander, Schmidt Anke, Kramer Axel, Metelmann Hans-Robert, Adler Frank, von Woedtke Thomas, Niessner Felix, Weltmann Klaus-Dieter, Wende Kristian
ZIK plasmatis, Leibniz-Institute for Plasma Science and Technology (INP Greifswald), Greifswald, Germany.
Institute for Hygiene and Environmental Medicine, University Medicine Greifswald, Greifswald, Germany.
Environ Mol Mutagen. 2018 May;59(4):268-277. doi: 10.1002/em.22172. Epub 2018 Feb 8.
Promising cold physical plasma sources have been developed in the field of plasma medicine. An important prerequisite to their clinical use is lack of genotoxic effects in cells. During optimization of one or even different plasma sources for a specific application, large numbers of samples need to be analyzed. There are soft and easy-to-assess markers for genotoxic stress such as phosphorylation of histone H2AX (γH2AX) but only few tests are accredited by the OECD with regard to mutagenicity detection. The micronucleus (MN) assay is among them but often requires manual counting of many thousands of cells per sample under the microscope. A high-throughput MN assay is presented using image flow cytometry and image analysis software. A human lymphocyte cell line was treated with plasma generated with ten different feed gas conditions corresponding to distinct reactive species patterns that were investigated for their genotoxic potential. Several millions of cells were automatically analyzed by a MN quantification strategy outlined in detail in this work. Our data demonstrates the absence of newly formed MN in any feed gas condition using the atmospheric pressure plasma jet kINPen. As positive control, ionizing radiation gave a significant 5-fold increase in micronucleus frequency. Thus, this assay is suitable to assess the genotoxic potential in large sample sets of cells exposed chemical or physical agents including plasmas in an efficient, reliable, and semiautomated manner. Environ. Mol. Mutagen. 59:268-277, 2018. © 2018 Wiley Periodicals, Inc.
在等离子体医学领域已开发出有前景的冷物理等离子体源。其临床应用的一个重要前提是在细胞中不存在遗传毒性效应。在针对特定应用优化一种甚至不同的等离子体源时,需要分析大量样本。有一些用于遗传毒性应激的易于评估的软标记物,例如组蛋白H2AX的磷酸化(γH2AX),但在诱变性检测方面,只有少数测试获得经合组织认可。微核(MN)试验就是其中之一,但通常需要在显微镜下对每个样本数千个细胞进行人工计数。本文介绍了一种使用图像流式细胞术和图像分析软件的高通量MN试验。用人淋巴细胞系处理由十种不同进料气体条件产生的等离子体,这些条件对应于不同的活性物种模式,并研究它们的遗传毒性潜力。通过本文详细概述的MN定量策略自动分析了数百万个细胞。我们的数据表明,使用大气压等离子体射流kINPen在任何进料气体条件下都没有新形成的MN。作为阳性对照,电离辐射使微核频率显著增加了5倍。因此,该试验适用于以高效、可靠和半自动的方式评估暴露于化学或物理剂(包括等离子体)的大量细胞样本集的遗传毒性潜力。《环境与分子突变》59:268 - 277,2018年。©2018威利期刊公司。