College of Animal Science and Technology, Northwest A&F University, Shaanxi 712100, China; Key Laboratory of Livestock Biology Northwest A&F University, Shaanxi 712100, China.
College of Animal Science and Technology, Northwest A&F University, Shaanxi 712100, China.
Food Res Int. 2023 May;167:112682. doi: 10.1016/j.foodres.2023.112682. Epub 2023 Mar 14.
Zinc oxide nanoparticles (ZnO NPs) have recently been used as food preservatives and additives because of their good antibacterial and nutritional functions. This study performed RNA-seq analyses to evaluate the potential toxicity of ZnO NPs on goat mammary epithelial cells (GMECs) in vitro. Our results suggested that the ZnO NP treatment significantly reduced GMEC viability in a time- and dose-dependent manner. Transcriptomic analysis showed that ZnO NP exposure changed the expression levels of more than 500 genes in GMECs, including various biological pathways. We observed that decreased mitochondrial membrane potential caused mitochondrial dysfunction. Further study indicated that the treatment of cells with ZnO NPs resulted in the accumulation of reactive oxygen species (ROS), which led to oxidative stress. Meanwhile, the expression of genes (TNFα, TNFR1, FADD, Caspase 8 and Caspase 6) associated with the death receptor pathway was upregulated, which indicated the death receptor-mediated extrinsic apoptosis pathway was activated. Moreover, the expression levels of Bax, Cytc, Caspase 3 and Caspase 9 were upregulated, while the expression levels of Bcl2 were downregulated, which indicated mitochondria-mediated intrinsic apoptosis pathway was activated. More notably, ZnO NP exposure increased the expression levels of ER stress-related genes (PERK, ATF4, eIF2α and CHOP) and proteins (p-PERK, p-eIF2α, PERK and CHOP). Furthermore, gene ontology (GO) terms and genes related to autophagy were altered, suggesting that exposure to ZnO NPs might activate autophagy in GMECs. In summary, our findings showed that ZnO NPs could exert significant toxic effects on GMECs through multiple mechanisms. These pathways are related to each other and influence each other to participate in ZnO NPs-induced the damage of GMECs. Thus, their safe use in the feed and food industry should be considered. Meanwhile, RNA-seq might represent a new method of assessing the toxicity mechanisms of nanomaterials.
氧化锌纳米粒子(ZnO NPs)由于其良好的抗菌和营养功能,最近被用作食品防腐剂和添加剂。本研究通过 RNA-seq 分析评估了 ZnO NPs 对体外山羊乳腺上皮细胞(GMECs)的潜在毒性。结果表明,ZnO NP 处理以时间和剂量依赖的方式显著降低 GMEC 的活力。转录组分析显示,ZnO NP 暴露改变了 GMECs 中超过 500 个基因的表达水平,包括各种生物途径。我们观察到线粒体膜电位降低导致线粒体功能障碍。进一步的研究表明,细胞用 ZnO NPs 处理导致活性氧(ROS)的积累,从而导致氧化应激。同时,与死亡受体途径相关的基因(TNFα、TNFR1、FADD、Caspase 8 和 Caspase 6)的表达上调,表明死亡受体介导的外在凋亡途径被激活。此外,Bax、Cytc、Caspase 3 和 Caspase 9 的表达水平上调,而 Bcl2 的表达水平下调,表明线粒体介导的内在凋亡途径被激活。更值得注意的是,ZnO NP 暴露增加了与内质网应激相关的基因(PERK、ATF4、eIF2α 和 CHOP)和蛋白质(p-PERK、p-eIF2α、PERK 和 CHOP)的表达水平。此外,基因本体(GO)术语和与自噬相关的基因发生改变,表明 ZnO NPs 暴露可能在 GMECs 中激活自噬。总之,我们的研究结果表明,ZnO NPs 可通过多种机制对 GMECs 产生显著的毒性作用。这些途径相互关联并相互影响,参与 ZnO NPs 诱导的 GMECs 损伤。因此,在饲料和食品工业中应考虑其安全使用。同时,RNA-seq 可能代表一种评估纳米材料毒性机制的新方法。