Institute of Biomedical Sciences, National Chung Hsing University, Taichung 40227, Taiwan; Graduate Institute of Basic Medicine, China Medical University, Taichung 40402, Taiwan; Department of Medical Research, China Medical University Hospital, Taichung 40402, Taiwan; Department of Biotechnology, Asia University, Taichung 41354, Taiwan.
Institute of Biomedical Sciences, National Chung Hsing University, Taichung 40227, Taiwan.
J Hazard Mater. 2014 Jan 15;264:303-12. doi: 10.1016/j.jhazmat.2013.11.031. Epub 2013 Nov 20.
Gold nanoparticles (AuNPs) possess unique properties that have been exploited in several medical applications. However, a more comprehensive understanding of the environmental safety of AuNPs is imperative for use of these nanomaterials. Here, we describe the impacts of AuNPs in various mammalian cell models using an automatic and dye-free method for continuous monitoring of cell growth based on the measurement of cell impedance. Several well-established cytotoxicity assays were also used for comparison. AuNPs induced a concentration-dependent decrease in cell growth. This inhibitory effect was associated with apoptosis induction in Vero cells but not in MRC-5 or NIH3T3 cells. Interestingly, cDNA microarray analyses in MRC-5 cells supported the involvement of DNA damage and repair responses, cell-cycle regulation, and oxidative stress in AuNP-induced cytotoxicity and genotoxicity. Moreover, autophagy appeared to play a role in AuNPs-induced attenuation of cell growth in NIH3T3 cells. In this study, we present a comprehensive overview of AuNP-induced cytotoxicity in a variety of mammalian cell lines, comparing several cytotoxicity assays. Collectively, these assays offer convincing evidence of the cytotoxicity of AuNPs and support the value of a systematic approach for analyzing the toxicology of nanoparticles.
金纳米颗粒(AuNPs)具有独特的性质,已在多种医学应用中得到了利用。然而,为了使用这些纳米材料,更全面地了解 AuNPs 的环境安全性是至关重要的。在这里,我们使用一种自动且无染料的方法描述了 AuNPs 在各种哺乳动物细胞模型中的影响,该方法基于细胞阻抗的测量来连续监测细胞生长。还使用了几种已建立的细胞毒性测定方法进行比较。AuNPs 诱导细胞生长呈浓度依赖性下降。这种抑制作用与 Vero 细胞中的细胞凋亡诱导有关,但与 MRC-5 或 NIH3T3 细胞无关。有趣的是,MRC-5 细胞中的 cDNA 微阵列分析支持 DNA 损伤和修复反应、细胞周期调控以及氧化应激参与了 AuNP 诱导的细胞毒性和遗传毒性。此外,自噬似乎在 AuNPs 诱导的 NIH3T3 细胞生长抑制中发挥作用。在这项研究中,我们全面概述了 AuNP 在多种哺乳动物细胞系中的细胞毒性,比较了几种细胞毒性测定方法。这些测定方法为 AuNPs 的细胞毒性提供了令人信服的证据,并支持系统方法分析纳米颗粒毒理学的价值。