Polystyrene nanoplastics trigger mitochondrial and metabolic reprogramming in cardiomyocytes: Evidence from integrated transcriptomic and metabolomic analysis

生物能学 线粒体 细胞生物学 氧化磷酸化 体内 代谢组学 活性氧 转录组 生物 细胞内 化学 TFAM公司 氧化应激 生物化学 脂质过氧化 线粒体毒性 离体 线粒体ROS 下调和上调 毒性 体外 TSG101型 线粒体DNA 线粒体分裂 药理学 线粒体生物发生 脂滴 微尺度热泳 污渍 重编程 程序性细胞死亡 DNA损伤
作者
Haitao Zhang,Huiting Cao,Yu Luo,Yunzhao Cao,Xianze Meng,Xinyu Wang,Ruidong Du,Xiwu Yan,Yun Gao,Zhuyuan Fang,Ming Liu
出处
期刊:Ecotoxicology and Environmental Safety [Elsevier BV]
卷期号:312: 119921-119921 被引量:1
标识
DOI:10.1016/j.ecoenv.2026.119921
摘要

Nanoplastics (NPs) are emerging environmental pollutants that can cross biological barriers due to their small size. Although numerous studies have investigated their effects in animal and cell models, multi-omics evaluations of their potential cardiovascular toxicity are still limited. To address this gap, we conducted a comprehensive assessment of polystyrene NPs (PS-NPs) using both in vitro and in vivo models. Human AC16 cardiomyocytes were exposed to PS-NPs and analyzed using RNA-seq, untargeted metabolomics, and functional assays. Transcriptomics revealed enrichment of mitochondrial-related genes and response to lipids, with pathways involving mitochondrial translation, ribosome function, and oxidative phosphorylation (OXPHOS). Bioenergetic profiling showed reduced basal and maximal oxygen consumption and ATP-linked respiration, accompanied by increased intracellular and mitochondrial reactive oxygen species (ROS). Untargeted metabolomics indicated broad lipid remodeling, particularly in glycerophospholipids, and alterations in nucleotide metabolism, consistent with energy dysregulation. For in vivo validation, mice received repeated tail vein injections of PS-NPs every 3 days for 2 weeks. Electron microscopy showed PS-NPs accumulation in cardiomyocytes and mitochondrial cristae disruption. Echocardiography revealed interventricular septal thickening with preserved ejection fraction and fractional shortening, suggesting subclinical remodeling. Myocardial ATP content decreased, and western blotting showed downregulation of OXPHOS complexes III-V and Pgc-1α. Although the chemical and particulate effects could not be distinguished in this study due to the lack of a particulate control, these results indicate that PS-NPs impair mitochondrial function and energy homeostasis in cardiomyocytes, suggesting potential cardiovascular hazards and highlighting the need for exposure monitoring in risk assessment.
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