Increased oxidative stress and activated heat shock proteins in human cell lines by silver nanoparticles

被引:42
作者
Xin, L. [1 ]
Wang, J. [2 ]
Wu, Y. [1 ]
Guo, S. [1 ]
Tong, J. [1 ]
机构
[1] Soochow Univ, Coll Med, Sch Publ Hlth, Suzhou 215123, Peoples R China
[2] KunShan Hlth Inspect Stn, Kunshan, Jiangsu, Peoples R China
基金
中国博士后科学基金;
关键词
Silver nanoparticles; oxidative damage; HSPAIA; HO-1; HEME OXYGENASE-1; HEAT-SHOCK-PROTEIN-70; TOXICITY; PATHWAY; CHAPERONES; EXPRESSION; INDUCTION; APOPTOSIS; EXPOSURE; MONOXIDE;
D O I
10.1177/0960327114538988
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Due to widely commercial applications of silver nanoparticles (Ag NPs), toxicity assessment of this NP is of great importance. This study aimed to investigate the oxidative stress and heat shock response of Ag NPs at different doses to A549 and HepG2 cells. After treatment with different concentrations of Ag NPs for 24 h, oxidative damage indicated by nnalondialdehyde (MDA), 8-epi-PGF2 alpha, and 8-hydroxy-2'-deoxyguanosine (8-oxo-dG) concentrations and protein levels of heat shock protein AIA (HSPAIA) and henne oxygenase 1 (HO-1) were determined. Ag NPs induced dose-dependent increases in MDA, 8-epi-PGF2a, and 8-oxo-dG concentrations in both A549 and HepG2 cells. Stress-inducible HSPAIA and HO-1 were also significantly upregulated in a dose-dependent manner. A higher level of HSPAIA and HO-1 activation by Ag NPs occurred in HepG2 cells than that in A549 cells. Compared with that of HSPAIA, Ag NPs induced a stronger increase in protein level of HO-1 in both cell lines. Significant positive correlations between protein levels of HSPAIA and HO-1 and oxidative damage were also observed. In conclusion, Ag NPs could induce oxidative stress in human cell lines. In addition to the products of oxidative stress such as MDA and 8-oxo-dG, HSPs can be used as potential biomarkers in nanotoxicity assessment, especially HO-1.
引用
收藏
页码:315 / 323
页数:9
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