Cytotoxicity, DNA damage, and apoptosis induced by titanium dioxide nanoparticles in human non-small cell lung cancer A549 cells

被引:116
作者
Wang, Yurong [1 ]
Cui, Haiyan [1 ]
Zhou, Jiaping [1 ]
Li, Fengjuan [1 ]
Wang, Jinju [1 ]
Chen, Mianhua [1 ]
Liu, Qingdai [1 ]
机构
[1] Tianjin Univ Sci & Technol, Sch Food Engn & Biotechnol, Minist Educ, Key Lab Food Nutr & Safety,TEDA, Tianjin 300457, Peoples R China
基金
中国国家自然科学基金;
关键词
Nanosized titanium dioxide; A549; cells; DNA damage; Apoptosis; Cytotoxicity; STRESS-MEDIATED CYTOTOXICITY; LONG-TERM EXPOSURE; OXIDATIVE STRESS; TIO2; NANOPARTICLES; EPITHELIAL-CELLS; PARTICLE-SIZE; IN-VIVO; PULMONARY INSTILLATION; FINE PARTICLES; ULTRAFINE TIO2;
D O I
10.1007/s11356-014-3717-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Concerns about the risk of titanium dioxide nanoparticles (TiO2 NPs) to human health and environment are gradually increasing due to their wide range of applications. In this study, cytotoxicity, DNA damage, and apoptosis induced by TiO2 NPs (5 nm) in A549 cells were investigated. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays revealed the time-and concentration-dependent cytotoxic effects of TiO2 NPs in a concentration range of 50 to 200 mu g/mL. A statistically significant (p<0.05) induction in DNA damage was observed by the comet assay in cells exposed to 50 to 200 mu g/mL TiO2 NPs for 48 h. A significant (p<0.05) induction in micronucleus formation determined by 4,6-diamino-2-phenylindole (DAPI) staining was also observed at the above concentrations. Typical apoptotic morphological feature and apoptotic bodies in A549 cells induced by TiO2 NPs at the above concentrations were observed by scanning electron micrographs. Flow cytometric analysis demonstrated that the cells treated with TiO2 NPs at concentrations of 100 and 200 mu g/mL showed a significant G(2)/M phase arrest and a significant increased proportion of apoptotic cells. TiO2 NPs also disrupted the mitochondrial membrane potential evaluated by rhodamine 123 staining. Further analysis by quantitative real-time PCR (qRT-PCR) indicated that the expression of caspase-3 and caspase-9 messenger RNA (mRNA) was increased significantly at the concentrations of 100 and 200 mu g/mL TiO2 NPs for 48 h. Taken together, these findings suggest that TiO2 NPs can inhibit A549 cell proliferation, cause DNA damage, and induce apoptosis via a mechanism primarily involving the activation of the intrinsic mitochondrial pathway. The assay data provide strong evidence that TiO2 NPs can induce cytotoxicity, significant DNA damage, and apoptosis of A549 cells, suggesting that exposure to TiO2 NPs could cause cell injury and be hazardous to health.
引用
收藏
页码:5519 / 5530
页数:12
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