规模较小,影响相同:在中等通量实验室复制高通量表型分析,用于化学品风险评估。

IF 6.9 2区 医学 Q1 TOXICOLOGY
Eunnara Cho, Stephen D. Baird, Kristin M. Eccles
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引用次数: 0

摘要

细胞绘画通过荧光染料染色细胞结构来观察毒性诱导的形态学变化。再加上高含量的成像和分析软件,细胞绘画允许高通量表型分析(HTPP)来量化表型变化和估计毒性评估的出发点。监管机构已将HTPP应用于384孔板进行化学危害筛选。在本研究中,384孔板的既定方案适用于96孔板,以增加低通量实验室的可及性。将U-2 OS人骨肉瘤细胞在96孔板中暴露于12种表型参比化合物24小时后固定并用荧光染料(高尔基体、内质网、核酸、细胞骨架、线粒体)染色。四种不同浓度的独立化学物质暴露产生了四种生物重复。染色细胞在高含量成像系统Opera Phenix上成像,Columbus分析软件提取1300个形态学特征的数值。将特征归一化到对照细胞,然后进行主成分分析和计算每个处理浓度的马氏倍数。模拟马氏比的距离来计算化学物质的基准浓度(BMC)。大多数bmc在实验中的差异小于一个数量级,表明实验室内部的一致性。与已发表的bmc相比,10种化合物在两种平板格式下具有可比的bmc。此外,我们观察到播种密度与马氏比目鱼距离之间存在显著的反比关系,这表明细胞密度等实验因素可能会影响bmc。总的来说,我们证明了细胞绘画在各种格式和实验室中都是适应性的,支持开发和验证它作为现有毒性测试的补充新方法方法的努力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Smaller scale, same impact: replicating high-throughput phenotypic profiling in a medium-throughput lab for use in chemical risk assessment

Cell Painting visualizes toxicity-induced morphological changes by staining cellular structures with fluorescent dyes. Coupled with high-content imaging and analysis software, Cell Painting allows high-throughput phenotypic profiling (HTPP) to quantify phenotypic changes and estimate points of departure for toxicity assessments. Regulatory agencies have applied HTPP in 384-well plates for chemical hazard screening. In this study, established protocols for 384-well plates were adapted for use in 96-well plates to increase accessibility for laboratories with lower throughput. U-2 OS human osteosarcoma cells in 96-well plates were exposed to 12 phenotypic reference compounds for 24 h before fixation and staining with fluorescent dyes (golgi apparatus, endoplasmic reticulum, nucleic acids, cytoskeleton, mitochondria). Four independent chemical exposures across eight concentrations generated four biological replicates. Stained cells were imaged on an Opera Phenix, a high-content imaging system, and the Columbus analysis software extracted numerical values for 1300 morphological features. Features were normalized to control cells, followed by principal component analysis and a calculation of Mahalanobis for each treatment concentration. Mahalanobis distances were modeled to calculate benchmark concentrations (BMC) for chemicals. Most BMCs differed by less than one order of magnitude across experiments, demonstrating intra-laboratory consistency. Compared to published BMCs, ten compounds had comparable BMCs in both plate formats. In addition, we observed a significant inverse relationship between seeding density and Mahalanobis distances, suggesting that experimental factors like cell density may influence BMCs. Overall, we demonstrate that Cell Painting is adaptable across formats and laboratories, supporting efforts to develop and validate it as a complementary new approach methodology to existing toxicity tests.

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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.
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