A multi-biomarker micronucleus assay using imaging flow cytometry.

IF 4.8 2区 医学 Q1 TOXICOLOGY
Archives of Toxicology Pub Date : 2024-09-01 Epub Date: 2024-07-12 DOI:10.1007/s00204-024-03801-7
Danielle S G Harte, Anthony M Lynch, Jatin Verma, Paul Rees, Andrew Filby, John W Wills, George E Johnson
{"title":"A multi-biomarker micronucleus assay using imaging flow cytometry.","authors":"Danielle S G Harte, Anthony M Lynch, Jatin Verma, Paul Rees, Andrew Filby, John W Wills, George E Johnson","doi":"10.1007/s00204-024-03801-7","DOIUrl":null,"url":null,"abstract":"<p><p>Genetic toxicity testing assesses the potential of compounds to cause DNA damage. There are many genetic toxicology screening assays designed to assess the DNA damaging potential of chemicals in early drug development aiding the identification of promising drugs that have low-risk potential for causing genetic damage contributing to cancer risk in humans. Despite this, in vitro tests generate a high number of misleading positives, the consequences of which can lead to unnecessary animal testing and/or the abandonment of promising drug candidates. Understanding chemical Mode of Action (MoA) is vital to identifying the true genotoxic potential of substances and, therefore, the risk translation into the clinic. Here we demonstrate a simple, robust protocol for staining fixed, human-lymphoblast p53 proficient TK6 cells with antibodies against ɣH2AX, p53 and pH3S28 along with DRAQ5™ DNA staining that enables analysis of un-lysed cells via microscopy approaches such as imaging flow cytometry. Here, we used the Cytek® Amnis® ImageStream®X Mk II which provides a high-throughput acquisition platform with the sensitivity of flow cytometry and spatial morphological information associated with microscopy. Using the ImageStream manufacturer's software (IDEAS® 6.2), a masking strategy was developed to automatically detect and quantify micronucleus events (MN) and characterise biomarker populations. The gating strategy developed enables the generation of a template capable of automatically batch processing data files quantifying cell-cycle, MN, ɣH2AX, p53 and pH3 populations simultaneously. In this way, we demonstrate how a multiplex system enables DNA damage assessment alongside MN identification using un-lysed cells on the imaging flow cytometry platform. As a proof-of-concept, we use the tool chemicals carbendazim and methyl methanesulphonate (MMS) to demonstrate the assay's ability to correctly identify clastogenic or aneugenic MoAs using the biomarker profiles established.</p>","PeriodicalId":8329,"journal":{"name":"Archives of Toxicology","volume":null,"pages":null},"PeriodicalIF":4.8000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11324684/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00204-024-03801-7","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/12 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Genetic toxicity testing assesses the potential of compounds to cause DNA damage. There are many genetic toxicology screening assays designed to assess the DNA damaging potential of chemicals in early drug development aiding the identification of promising drugs that have low-risk potential for causing genetic damage contributing to cancer risk in humans. Despite this, in vitro tests generate a high number of misleading positives, the consequences of which can lead to unnecessary animal testing and/or the abandonment of promising drug candidates. Understanding chemical Mode of Action (MoA) is vital to identifying the true genotoxic potential of substances and, therefore, the risk translation into the clinic. Here we demonstrate a simple, robust protocol for staining fixed, human-lymphoblast p53 proficient TK6 cells with antibodies against ɣH2AX, p53 and pH3S28 along with DRAQ5™ DNA staining that enables analysis of un-lysed cells via microscopy approaches such as imaging flow cytometry. Here, we used the Cytek® Amnis® ImageStream®X Mk II which provides a high-throughput acquisition platform with the sensitivity of flow cytometry and spatial morphological information associated with microscopy. Using the ImageStream manufacturer's software (IDEAS® 6.2), a masking strategy was developed to automatically detect and quantify micronucleus events (MN) and characterise biomarker populations. The gating strategy developed enables the generation of a template capable of automatically batch processing data files quantifying cell-cycle, MN, ɣH2AX, p53 and pH3 populations simultaneously. In this way, we demonstrate how a multiplex system enables DNA damage assessment alongside MN identification using un-lysed cells on the imaging flow cytometry platform. As a proof-of-concept, we use the tool chemicals carbendazim and methyl methanesulphonate (MMS) to demonstrate the assay's ability to correctly identify clastogenic or aneugenic MoAs using the biomarker profiles established.

Abstract Image

利用成像流式细胞仪进行多生物标记微核检测。
遗传毒性测试评估化合物造成 DNA 损伤的可能性。有许多遗传毒理学筛选试验旨在评估早期药物开发过程中化学品的 DNA 损伤潜力,以帮助识别有潜力的药物,这些药物在导致人类癌症风险的遗传损伤方面风险较低。尽管如此,体外试验仍会产生大量误导性阳性结果,其后果可能导致不必要的动物试验和/或放弃有前途的候选药物。了解化学作用模式(MoA)对于确定物质的真正遗传毒性潜力,从而将风险转化到临床中至关重要。在这里,我们展示了一种简单、稳健的方案,即用针对ɣH2AX、p53 和 pH3S28 的抗体对固定的、具有 p53 能力的人类淋巴细胞 TK6 细胞进行染色,同时进行 DRAQ5™ DNA 染色,从而通过成像流式细胞仪等显微镜方法对未裂解的细胞进行分析。在这里,我们使用了 Cytek® Amnis® ImageStream®X Mk II,它提供了一个高通量采集平台,具有流式细胞仪的灵敏度和显微镜的空间形态信息。利用 ImageStream 制造商的软件(IDEAS® 6.2),开发了一种屏蔽策略,用于自动检测和量化微核事件(MN),并描述生物标记群的特征。所开发的屏蔽策略能够生成一个模板,自动批量处理数据文件,同时量化细胞周期、MN、ɣH2AX、p53 和 pH3 群体。通过这种方式,我们展示了多重系统如何在成像流式细胞仪平台上使用未裂解细胞进行 DNA 损伤评估和 MN 鉴定。作为概念验证,我们使用工具化学品多菌灵和甲基甲磺酸甲酯(MMS)来证明该检测方法有能力利用所建立的生物标记图谱正确识别致克隆性或非遗传性MoAs。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Archives of Toxicology
Archives of Toxicology 医学-毒理学
CiteScore
11.60
自引率
4.90%
发文量
218
审稿时长
1.5 months
期刊介绍: Archives of Toxicology provides up-to-date information on the latest advances in toxicology. The journal places particular emphasis on studies relating to defined effects of chemicals and mechanisms of toxicity, including toxic activities at the molecular level, in humans and experimental animals. Coverage includes new insights into analysis and toxicokinetics and into forensic toxicology. Review articles of general interest to toxicologists are an additional important feature of the journal.
文献相关原料
公司名称 产品信息 采购帮参考价格
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信