Genotoxicity of multi-walled carbon nanotubes in both in vitro and in vivo assay systems

被引:76
作者
Kato, Tatsuya [1 ,2 ]
Totsuka, Yukari [1 ]
Ishino, Kousuke [1 ]
Matsumoto, Yoko [1 ,3 ]
Tada, Yukie [4 ]
Nakae, Dai [5 ,6 ]
Goto, Sumio [3 ]
Masuda, Shuichi [2 ]
Ogo, Sayaka [7 ]
Kawanishi, Masanobu [7 ]
Yagi, Takashi [7 ]
Matsuda, Tomonari [8 ]
Watanabe, Masatoshi [9 ]
Wakabayashi, Keiji [2 ]
机构
[1] Natl Canc Ctr, Res Inst, Div Canc Dev Syst, Chuo Ku, Tokyo 104, Japan
[2] Univ Shizuoka, Grad Sch Nutr & Environm Sci, Shizuoka 4228526, Japan
[3] Azabu Univ, Sch Life & Environm Sci, Lab Environm Risk Evaluat, Sagamihara, Kanagawa, Japan
[4] Tokyo Metropolitan Inst Publ Hlth, Dept Environm Hlth & Toxicol, Shinjuku Ku, Tokyo 1690073, Japan
[5] Tokyo Metropolitan Inst Publ Hlth, Dept Pharmaceut Sci, Shinjuku Ku, Tokyo 1690073, Japan
[6] Tokyo Univ Agr, Setagaya Ku, Tokyo 1568502, Japan
[7] Osaka Prefecture Univ, Grad Sch Sci, Sakai, Osaka 591, Japan
[8] Kyoto Univ, Res Ctr Environm Qual Management, Otsu, Shiga, Japan
[9] Yokohama Natl Univ, Grad Sch Engn, Div Mat Sci & Engn, Hodogaya Ku, Yokohama, Kanagawa 240, Japan
关键词
Micronuclei; sister chromatid exchange; DNA damage; gpt mutation; oxidative stress; OXYGEN SPECIES PRODUCTION; MALE FISCHER-344 RATS; OXIDATIVE DNA-DAMAGE; LIPID-PEROXIDATION; MAMMALIAN-CELLS; PULMONARY TOXICITY; EPITHELIAL-CELLS; NITRIC-OXIDE; MUTATION; INHALATION;
D O I
10.3109/17435390.2012.674571
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The genotoxic effects of multi-walled carbon nanotubes (MWCNTs) were examined by using in vitro and in vivo assays. MWCNTs significantly induced micronuclei in A549 cells and enhanced the frequency of sister chromatid exchange (SCE) in CHO AA8 cells. When ICR mice were intratracheally instilled with a single dose (0.05 or 0.2 mg/animal) of MWCNTs, DNA damage of the lungs, analysed by comet assay, increased in a dose-dependent manner. Moreover, DNA oxidative damage, indicated by 8-oxo-7,8-dihydro-2'-deoxyguanosine and heptanone etheno-deoxyribonucleosides, occurred in the lungs of MWCNT-exposed mice. The gpt mutation frequencies significantly increased in the lungs of MWCNT-treated gpt delta transgenic mice. Transversions were predominant, and G: C to C: G was clearly increased by MWCNTs. Moreover, many regions immunohistochemically stained for inducible NO synthase and nitrotyrosine were observed in the lungs of MWCNT-exposed mice. Overall, MWCNTs were shown to be genotoxic both in in vitro and in vivo tests; the mechanisms probably involve oxidative stress and inflammatory responses.
引用
收藏
页码:452 / 461
页数:10
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