Effect of titanium dioxide nanoparticles on DNA methylation of human peripheral blood mononuclear cells

被引:5
|
作者
Malakootian, Mohammad [1 ]
Nasiri, Alireza [1 ]
Osornio-Vargas, Alvaro R. [2 ]
Faraji, Maryam [1 ,3 ]
机构
[1] Kerman Univ Med Sci, Environm Hlth Engn Res Ctr, Kerman, Iran
[2] Univ Alberta, Dept Pediat, 3-591 Edmonton Clin Hlth Acad, Edmonton, AB T6G 1C9, Canada
[3] Kerman Univ Med Sci, Fac Publ Hlth, Dept Environm Hlth Engn, Kerman, Iran
基金
美国国家科学基金会;
关键词
titanium dioxide nanoparticles; DNA methylation; epigenetic genotoxicity; OXIDATIVE STRESS; LUNG FIBROBLASTS; DUST STORM; TIO2; CYTOTOXICITY; NANOTOXICITY; INDUCTION; EXPOSURE; IMPACT; METAL;
D O I
10.1093/toxres/tfab085
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The aim of the current study was to investigate the effect of well-characterized TiO2 nanoparticles on DNA methylation of peripheral blood mononuclear cells (PBMCs) in vitro. Maximum non-toxic concentration of nanoparticles for PBMCs was determined by MTT assay. The effect of TiO2 nanoparticles at concentrations of 25-100 mu g/ml on DNA methylation of PBMCs was investigated by measuring the %5-mC alterations through an ELISA assay. The physicochemical analysis showed that the TiO2 nanoparticles were crystalline, pure and in the anatase phase. Peaks related to Ti-O tensile vibrations were observed in the range of 1510 cm(-1). The size of nanoparticles was in the range of 39-74 nm with an average hydrodynamic diameter of 43.82 nm. According to the results of the MTT test, 100 mu g/ml was found to be maximum non-toxic concentration. The %5-mC in treated PBMCs revealed that TiO2 nanoparticles could lead to DNA hypomethylation in PBMCs. The %5-mC difference compared with the negative control was found to be 2.07 +/- 1.02% (P = 0.03). The difference of %5-mC between the 25 and 100 pg/ml concentration of nanoparticles was statistically significant (P = 0.02). The results of the current study show that the TiO2 nanoparticles cause DNA hypomethylation in PBMCs in a dose-response manner. Therefore, it is recommended to evaluate the effects of cytotoxicity and epigenotoxicity of commonly used nanoparticles before their use.
引用
收藏
页码:1045 / 1051
页数:7
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