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Evaluation of 309 Environmental Chemicals Using a Mouse Embryonic Stem Cell Adherent Cell Differentiation and Cytotoxicity Assay

机译:使用小鼠胚胎干细胞贴壁细胞分化和细胞毒性分析评估309种环境化学品

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摘要

The vast landscape of environmental chemicals has motivated the need for alternative methods to traditional whole-animal bioassays in toxicity testing. Embryonic stem (ES) cells provide an in vitro model of embryonic development and an alternative method for assessing developmental toxicity. Here, we evaluated 309 environmental chemicals, mostly food-use pesticides, from the ToxCast™ chemical library using a mouse ES cell platform. ES cells were cultured in the absence of pluripotency factors to promote spontaneous differentiation and in the presence of DMSO-solubilized chemicals at different concentrations to test the effects of exposure on differentiation and cytotoxicity. Cardiomyocyte differentiation (α,β myosin heavy chain; MYH6/MYH7) and cytotoxicity (DRAQ5™/Sapphire700™) were measured by In-Cell Western™ analysis. Half-maximal activity concentration (AC50) values for differentiation and cytotoxicity endpoints were determined, with 18% of the chemical library showing significant activity on either endpoint. Mining these effects against the ToxCast Phase I assays (∼500) revealed significant associations for a subset of chemicals (26) that perturbed transcription-based activities and impaired ES cell differentiation. Increased transcriptional activity of several critical developmental genes including BMPR2, PAX6 and OCT1 were strongly associated with decreased ES cell differentiation. Multiple genes involved in reactive oxygen species signaling pathways (NRF2, ABCG2, GSTA2, HIF1A) were strongly associated with decreased ES cell differentiation as well. A multivariate model built from these data revealed alterations in ABCG2 transporter was a strong predictor of impaired ES cell differentiation. Taken together, these results provide an initial characterization of metabolic and regulatory pathways by which some environmental chemicals may act to disrupt ES cell growth and differentiation.
机译:环境化学的广阔前景激发了对毒性测试中传统的全动物生物测定方法的替代方法的需求。胚胎干(ES)细胞提供了胚胎发育的体外模型和评估发育毒性的替代方法。在这里,我们使用小鼠ES细胞平台从ToxCast™化学文库中评估了309种环境化学品,主要是食用农药。在不存在能促进自发分化的多能性因子和不同浓度的DMSO增溶的化学物质的情况下培养ES细胞,以测试暴露对分化和细胞毒性的影响。通过In-Cell Western TM分析测量心肌细胞分化(α,β肌球蛋白重链; MYH6 / MYH7)和细胞毒性(DRAQ5 TM / Sapphire 700 TM)。确定了分化和细胞毒性终点的半数最大活性浓度(AC50)值,其中18%的化学文库在任一终点上均显示出显着活性。针对ToxCast I期分析(约500个)挖掘这些影响,发现与扰乱基于转录的活性并损害ES细胞分化的一组化学物质(26种)之间存在显着关联。包括BMPR2,PAX6和OCT1在内的几个关键发育基因的转录活性增强与ES细胞分化降低密切相关。参与活性氧信号通路的多个基因(NRF2,ABCG2,GSTA2,HIF1A)也与减少的ES细胞分化密切相关。根据这些数据建立的多变量模型显示,ABCG2转运蛋白的改变是ES细胞分化受损的有力预测指标。综上所述,这些结果提供了代谢和调节途径的初步表征,某些环境化学物质可能通过这些途径破坏ES细胞的生长和分化。

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