Bernacki Derek T, Bryce Steven M, Bemis Jeffrey C, Kirkland David, Dertinger Stephen D
Litron Laboratories, 3500 Winton Place, Rochester, New York, 14623, USA.
Kirkland Consulting, Tadcaster, UK.
Environ Mol Mutagen. 2016 Aug;57(7):546-558. doi: 10.1002/em.22028. Epub 2016 Jul 1.
Previous work with a diverse set of reference chemicals suggests that an in vitro multiplexed flow cytometry-based assay (MultiFlow™ DNA Damage Kit-p53, γH2AX, Phospho-Histone H3) can distinguish direct-acting clastogens and aneugens from nongenotoxicants (Bryce SM et al. []: Environ Mol Mutagen 57:171-189). This work extends this line of investigation to include compounds that require metabolic activation to form reactive electrophiles. For these experiments, TK6 cells were exposed to 11 promutagens and 37 presumed nongenotoxicants in 96 well plates. Unless precipitation or foreknowledge about cytotoxicity suggested otherwise, the highest concentration was 1 mM. Exposure occurred for 4 hr after which time cells were washed to remove S9 and test article. Immediately following the wash and again at 24 hr, cell aliquots were added to wells of a microtiter plate containing the working detergent/stain/antibody cocktail. After a brief incubation, robotic sampling was employed for walk-away flow cytometric data acquisition. Univariate logistic regression analyses indicated that γH2AX induction and p53 activation provide the greatest degree of discrimination between clastogens and nongenotoxicants. Multivariate prediction algorithms that incorporated both of these endpoints, in each combination of time points, were evaluated. The best performing models correctly predicted 9 clastogens out of 11 and 36 nongenotoxicants out of 37. These results are encouraging as they suggest that an efficient and highly scalable multiplexed assay can effectively identify clastogenic chemicals that require bioactivation. More work is planned with a broader range of chemicals, additional cell lines, and other laboratories to further evaluate the merits and limitations of this approach. Environ. Mol. Mutagen. 57:546-558, 2016. © 2016 Wiley Periodicals, Inc.
此前针对多种参考化学品开展的研究表明,基于体外多重流式细胞术的检测方法(MultiFlow™ DNA损伤检测试剂盒——检测p53、γH2AX、磷酸化组蛋白H3)能够区分直接作用的致断裂剂和非整倍体剂与非遗传毒性剂(Bryce SM等人[文献引用]:《环境与分子突变》57卷:171 - 189页)。本研究将这一研究方向扩展至包括需要代谢活化以形成反应性亲电试剂的化合物。在这些实验中,将TK6细胞接种于96孔板中,分别暴露于11种前诱变剂和37种假定的非遗传毒性剂。除非出现沉淀或已知有细胞毒性,否则最高浓度设定为1 mM。暴露4小时后,洗涤细胞以去除S9和受试物。洗涤后立即以及在24小时时,将细胞 aliquots添加至含有工作去污剂/染色剂/抗体混合物的微量滴定板孔中。短暂孵育后,采用机器人采样进行自动流式细胞术数据采集。单变量逻辑回归分析表明,γH2AX诱导和p53激活在区分致断裂剂和非遗传毒性剂方面具有最大程度的辨别力。对在每个时间点组合中纳入这两个终点的多变量预测算法进行了评估。表现最佳的模型正确预测出了11种致断裂剂中的9种以及37种非遗传毒性剂中的36种。这些结果令人鼓舞,因为它们表明一种高效且高度可扩展的多重检测方法能够有效识别需要生物活化的致断裂化学物质。计划开展更多研究,涉及更广泛的化学品、更多细胞系以及其他实验室,以进一步评估该方法的优点和局限性。《环境与分子突变》57卷:546 - 558页,2016年。© 2016威利期刊公司