中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Fast intracellular dissolution and persistent cellular uptake of silver nanoparticles in CHO-K1 cells: implication for cytotoxicity

文献类型:期刊论文

作者Jiang, XM; Miclaus, T; Wang LM(王黎明); Wang, LM; Foldbjerg, R; Sutherland, DS; Autrup, H; Chen, CY; Beer, C
刊名NANOTOXICOLOGY
出版日期2015
卷号9期号:2页码:181-189
关键词Degradation N-acetyl-L-cysteine reactive oxygen species silver nanoparticles uptake pathway XANES
英文摘要Toxicity of silver nanoparticles (Ag NPs) has been reported both in vitro and in vivo. However, the intracellular stability and chemical state of Ag NPs are still not very well studied. In this work, we systematically investigated the cellular uptake pathways, intracellular dissolution and chemical species, and cytotoxicity of Ag NPs (15.9 +/- 7.6 nm) in Chinese hamster ovary cell subclone K1 cells, a cell line recommended by the OECD for genotoxicity studies. Quantification of intracellular nanoparticle uptake and ion release was performed through inductively coupled plasma mass spectrometry. X-ray absorption near-edge structure (XANES) was employed to assess the chemical state of intracellular silver. The toxic potential of Ag NPs and Ag+ was evaluated by cell viability, reactive oxygen species (ROS) production and live-dead cell staining. The results suggest that cellular uptake of Ag NPs involves lipid-raft-mediated endocytosis and energy-independent diffusion. The degradation study shows that Ag NPs taken up into cells dissolved quickly and XANES results directly indicated that the internalized Ag was oxidized to Ag-O- species and then stabilized in silver-sulfur (Ag-S-) bonds within the cells. Subsequent cytotoxicity studies show that Ag NPs decrease cell viability and increase ROS production. Pre-incubation with N-acetyl-L-cysteine, an efficient antioxidant and Ag+ chelator, diminished the cytotoxicity caused by Ag NPs or Ag+ exposure. Our study suggests that the cytotoxicity mechanism of Ag NPs is related to the intracellular release of silver ions, followed by their binding to SH-groups, presumably coming from amino acids or proteins, and affecting protein functions and the antioxidant defense system of cells.
学科主题Science & Technology - Other Topics; Toxicology
类目[WOS]Nanoscience & Nanotechnology ; Toxicology
收录类别SCI
WOS记录号WOS:000351947700006
公开日期2016-05-03
源URL[http://ir.ihep.ac.cn/handle/311005/228380]  
专题中国科学院高能物理研究所
推荐引用方式
GB/T 7714
Jiang, XM,Miclaus, T,Wang LM,et al. Fast intracellular dissolution and persistent cellular uptake of silver nanoparticles in CHO-K1 cells: implication for cytotoxicity[J]. NANOTOXICOLOGY,2015,9(2):181-189.
APA Jiang, XM.,Miclaus, T.,王黎明.,Wang, LM.,Foldbjerg, R.,...&Beer, C.(2015).Fast intracellular dissolution and persistent cellular uptake of silver nanoparticles in CHO-K1 cells: implication for cytotoxicity.NANOTOXICOLOGY,9(2),181-189.
MLA Jiang, XM,et al."Fast intracellular dissolution and persistent cellular uptake of silver nanoparticles in CHO-K1 cells: implication for cytotoxicity".NANOTOXICOLOGY 9.2(2015):181-189.

入库方式: OAI收割

来源:高能物理研究所

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