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尺寸依赖的 ZnO 纳米颗粒在 HepG2 细胞中的细胞毒性研究。

Size-dependent cytotoxicity study of ZnO nanoparticles in HepG2 cells.

机构信息

Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, China.

Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, China.

出版信息

Ecotoxicol Environ Saf. 2019 Apr 30;171:337-346. doi: 10.1016/j.ecoenv.2018.12.096. Epub 2019 Jan 4.

Abstract

Zinc oxide (ZnO) nanoparticles (NPs) are widely used in daily life. However, common utilization of ZnO NPs results in increases in environmental release, and their health hazards have attracted extensive attention. To investigate the cytotoxicity of ZnO NPs and their mechanism in HepG2 cells, a comprehensive analytical system was developed. The internalization, cytotoxic mechanism, death mechanism and elimination behavior of three sizes of ZnO NPs were studied by electrothermal vaporization (ETV)-inductively coupled plasma mass spectrometry (ICP-MS), MTT assays, GSH measurements, ROS measurements and analyses of apoptosis and gene expression. The size-, dose- and time-dependent characteristics of ZnO NPs were determined, and the metabolism of ZnO NPs in cells was discussed. The cytotoxicity of ZnO NPs was confirmed to depend on both the size and concentration and was attributed to the release of Zn, induction of oxidative stress and inflammatory response; the death mode of HepG2 cells incubated with ZnO NPs was necrotic rather than programmed cell death.

摘要

氧化锌 (ZnO) 纳米粒子 (NPs) 在日常生活中被广泛应用。然而,由于 ZnO NPs 的普遍使用导致其在环境中的释放增加,其健康危害引起了广泛关注。为了研究 ZnO NPs 的细胞毒性及其在 HepG2 细胞中的作用机制,建立了一个全面的分析系统。通过电热蒸发 (ETV)-电感耦合等离子体质谱 (ICP-MS)、MTT 测定、GSH 测量、ROS 测量以及细胞凋亡和基因表达分析,研究了三种尺寸 ZnO NPs 的内化、细胞毒性机制、死亡机制和消除行为。确定了 ZnO NPs 的尺寸、剂量和时间依赖性特征,并讨论了其在细胞内的代谢情况。研究证实,ZnO NPs 的细胞毒性取决于其尺寸和浓度,这归因于 Zn 的释放、氧化应激和炎症反应的诱导;与 ZnO NPs 孵育的 HepG2 细胞的死亡模式为坏死而不是程序性细胞死亡。

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