Cytotoxicity of water-soluble mPEG-SH-coated silver nanoparticles in HL-7702 cells

被引:28
作者
Song, Xiu-ling [1 ]
Li, Bo [1 ]
Xu, Kun [1 ]
Liu, Juan [2 ]
Ju, Wen [1 ]
Wang, Juan [1 ]
Liu, Xiao-dong [1 ]
Li, Juan [1 ]
Qi, Yan-fei [1 ]
机构
[1] Jilin Univ, Sch Publ Hlth, Dept Toxicol, Changchun 130021, Peoples R China
[2] PLA, Hosp 208, Changchun 130062, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Silver nanoparticles; Cytotoxicity; Oxidative stress; Mitochondrial membrane potential; Cell cycle; DNA-DAMAGE; OXIDATIVE STRESS; TOXICITY; NANOSILVER; PARTICLES; APOPTOSIS; RESPONSES; EXPOSURE; GENOTOXICITY; RATS;
D O I
10.1007/s10565-012-9218-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Silver nanoparticles (AgNPs) are being used widely and increasingly in various products and medical supplies due to their antibacterial activity. However, little is known about the impacts of the AgNPs. Herein, The primary purpose of this study was to investigate the cytotoxic effect of AgNPs in the human liver cell line (HL-7702). The water-soluble alpha-Methoxy-poly (ethylene glycol)-omega-mercapto (mPEG-SH)-coated AgNPs (40 nm) were synthesized, which showed superior stabilization and uniform dispersion in culture medium. The effect of mPEG-SH-coated silver nanoparticles on cell viability, leakage of lactate dehydrogenase (LDH), oxidative stress, mitochondrial membrane potential (MMP), and cell cycle was evaluated after the cells were treated with nanoparticles. The results showed that the coated AgNPs could be taken up by cells, decreased cell viability in dose- and time-dependent manners at dosage levels between 6.25 and 100.00 mu g/mL, caused membrane damage (LDH leakage), and decreased the activities of superoxide dismutase and glutathione peroxides. The level of malondialdehyde, an end product of lipid peroxidation, was also increased in AgNPs-exposed cells. Moreover, flow cytometric analysis showed that AgNP exposure decrease MMP and cause G(2)/M phase arrest. Thus, our data suggest that mPEG-SH-coated AgNPs have the potential toxicity that is associated with oxidative stress, apoptosis, and DNA damage.
引用
收藏
页码:225 / 237
页数:13
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