Sirenko Oksana, Grimm Fabian A, Ryan Kristen R, Iwata Yasuhiro, Chiu Weihsueh A, Parham Frederick, Wignall Jessica A, Anson Blake, Cromwell Evan F, Behl Mamta, Rusyn Ivan, Tice Raymond R
Molecular Devices, LLC, Sunnyvale, CA, USA.
Department of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX, USA.
Toxicol Appl Pharmacol. 2017 May 1;322:60-74. doi: 10.1016/j.taap.2017.02.020. Epub 2017 Mar 1.
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 30min or 24h and effects on cardiomyocyte beating and cellular and mitochondrial toxicity were assessed by kinetic measurements of intracellular Ca 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 the tested chemicals exhibited effects on cardiomyocyte beating after 30min of exposure. In contrast, after 24h, effects on cell beating without concomitant cytotoxicity were observed in about one third of the compounds. Concentration-response data for in vitro bioactivity phenotypes visualized using the Toxicological Prioritization Index (ToxPi) 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 at high exposure levels to alter cardiomyocyte function, but also indicate similarities in the mechanism of these effects both within and among chemicals and classes.
通过体外筛选来填补数据空白的一个重要目标领域是检测潜在的心脏毒性物质。尽管目前保守估计所有心血管疾病病例中至少23%与环境暴露有关,但致病因子的身份在很大程度上仍未明确。在此,我们使用包含69种代表性环境化学品和药物的文库,评估一种组合体外/计算机模拟筛选方法用于环境危害的功能性和机制性心脏毒性分析的可行性。将人诱导多能干细胞衍生的心肌细胞进行浓度响应暴露30分钟或24小时,并通过细胞内钙通量的动力学测量以及使用核染料Hoechst 33342、细胞活力标记物Calcein AM和线粒体去极化探针JC-10的高内涵成像来评估对心肌细胞跳动以及细胞和线粒体毒性的影响。超过一半的受试化学品在暴露30分钟后对心肌细胞跳动产生影响。相比之下,在24小时后,约三分之一的化合物观察到对细胞跳动有影响但无伴随的细胞毒性。使用毒理学优先排序指数(ToxPi)可视化的体外生物活性表型的浓度响应数据显示环境化学品(包括农药、阻燃剂和多环芳烃)的化学类别特异性聚类。对于具有人类暴露预测的环境化学品,模拟血药浓度与体外生物活性之间的活性-暴露比在1至5个数量级之间。这些发现不仅表明一些普遍存在的环境污染物在高暴露水平下可能有改变心肌细胞功能的潜力,而且还表明这些影响在化学品及其类别内部和之间的机制具有相似性。