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In vitro cardiotoxicity assessment of environmental chemicals using an organotypic human induced pluripotent stem cell-derived model

机译:使用器官型人诱导多能干细胞衍生模型对环境化学品进行体外心脏毒性评估

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摘要

An important target area for addressing data gaps through in vitro screening is the detection of potential cardiotoxicants. Despite the fact that current conservative estimates relate at least 23% of all cardiovascular disease cases to environmental exposures, the identities of the causative agents remain largely uncharacterized. Here, we evaluate the feasibility of a combinatorial in vitro/in silico screening approach for functional and mechanistic cardiotoxicity profiling of environmental hazards using a library of 69 representative environmental chemicals and drugs. Human induced pluripotent stem cell-derived cardiomyocytes were exposed in concentration-response for 30 min or 24 hrs and effects on cardiomyocyte beating and cellular and mitochondrial toxicity were assessed by kinetic measurements of intracellular Ca2+ flux and high-content imaging using the nuclear dye Hoechst 33342, the cell viability marker Calcein AM, and the mitochondrial depolarization probe JC-10. More than half of tested chemicals exhibited effects on cardiomyocyte rhythm after 30 min of exposure. After 24 hours, the effects on cell rhythm without cytotoxicity were observed in about one third of the compounds. Concentration-response data for in vitro bioactivity phenotypes were visualized using Toxicological Prioritization Index (ToxPi) and showed chemical class-specific clustering of environmental chemicals, including pesticides, flame retardants, and polycyclic aromatic hydrocarbons. For environmental chemicals with human exposure predictions, the activity-to-exposure ratios between modeled blood concentrations and in vitro bioactivity were between one and five orders of magnitude. These findings not only demonstrate that some ubiquitous environmental pollutants might have the potential to alter cardiomyocyte function at high exposures, but also indicate similarities in the mechanism of these effects both within and among chemicals and classes.
机译:通过体外筛选解决数据缺口的重要目标领域是潜在心脏毒性剂的检测。尽管目前的保守估计至少占所有心血管疾病病例的23%与环境暴露有关,但致病因素的身份在很大程度上仍未发现。在这里,我们使用69种代表性的环境化学药品和药物库,评估了组合的体外/计算机模拟筛查方法对环境危害的功能和机制心脏毒性特征分析的可行性。将人类诱导的多能干细胞衍生的心肌细胞进行浓度反应30分钟或24小时,并通过细胞内Ca 2 + 通量和高动力学测量动力学评估对心肌细胞跳动以及细胞和线粒体毒性的影响核染料Hoechst 33342,细胞活力标记钙黄绿素AM和线粒体去极化探针JC-10进行高含量成像。暴露30分钟后,超过一半的受测化学物质对心肌细胞节律有影响。 24小时后,在约三分之一的化合物中观察到对细胞节律的影响而没有细胞毒性。使用毒理学优先排序指数(ToxPi)可视化了体外生物活性表型的浓度响应数据,并显示了环境化学物(包括农药,阻燃剂和多环芳烃)的特定于化学类别的聚类。对于具有人类暴露预测的环境化学药品,建模的血药浓度与体外生物活性之间的活性与暴露比介于1个和5个数量级之间。这些发现不仅表明某些普遍存在的环境污染物在高暴露量下可能具有改变心肌细胞功能的潜力,而且还表明在化学物质和类别之间以及这些类别之间,这些作用机理的相似性。

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