Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing, Jiangsu 210009, China.
Institute of Biomedical Devices (Suzhou), Southeast University, Suzhou 215163, China.
ACS Nano. 2024 Nov 12;18(45):31569-31585. doi: 10.1021/acsnano.4c13262. Epub 2024 Nov 1.
Exposure to micro- and nanoplastics (MNPs) has been implicated in potential cardiotoxicity. However, in vitro models based on cardiomyocyte cell lines lack crucial cardiac characteristics, while interspecies differences in animal models compromise the reliability of the conclusions. In addition, current research has predominantly focused on single-time point exposures to MNPs, neglecting comparative analyses of cardiac injury across early and late stages. Moreover, there remains a large gap in understanding the susceptibility to MNPs under pathological conditions. To address these limitations, this study integrated cardiac organoids (COs) and organ-on-a-chip (OoC) technology to develop the cardiac organoid-on-a-chip (COoC), which was validated for cardiotoxicity evaluation through multiple dimensions. Based on COoC, we conducted a dynamic observation of the cardiac damage caused by short- and long-term exposure to polystyrene nanoplastics (PS-NPs). Oxidative stress, inflammation, disruption of calcium ion homeostasis, and mitochondrial dysfunction were confirmed as the potential mechanisms of PS-NP-induced cardiotoxicity and the crucial events in the early stages, while cardiac fibrosis emerged as a prominent feature in late stages. Notably, low-dose exposure exacerbated myocardial infarction symptoms under pathological states, despite no significant cardiotoxicity shown in healthy models. In conclusion, these findings further deepened our understanding of PS-NP-induced cardiotoxic effects and introduced a promising in vitro platform for assessing cardiotoxicity.
暴露于微塑料和纳米塑料(MNPs)已被认为与潜在的心脏毒性有关。然而,基于心肌细胞系的体外模型缺乏关键的心脏特征,而动物模型中的种间差异则影响了结论的可靠性。此外,目前的研究主要集中在 MNPs 的单次暴露,而忽略了对早期和晚期心脏损伤的比较分析。此外,对于在病理条件下对 MNPs 的易感性,我们的理解仍然存在很大差距。为了解决这些局限性,本研究整合了心脏类器官(COs)和器官芯片(OoC)技术,开发了心脏类器官芯片(COoC),并通过多个维度验证了其用于心脏毒性评估的适用性。基于 COoC,我们对聚苯乙烯纳米塑料(PS-NPs)短期和长期暴露引起的心脏损伤进行了动态观察。氧化应激、炎症、钙离子内稳态紊乱和线粒体功能障碍被确认为 PS-NP 诱导心脏毒性的潜在机制和早期的关键事件,而心脏纤维化则成为晚期的一个显著特征。值得注意的是,在病理状态下,低剂量暴露加剧了心肌梗死症状,尽管在健康模型中没有显示出明显的心脏毒性。总之,这些发现进一步加深了我们对 PS-NP 诱导的心脏毒性作用的理解,并引入了一种有前途的体外心脏毒性评估平台。