Division of Cancer Development System, National Cancer Center Research Institute, Chuo-ku, Tokyo, Japan.
Nanotoxicology. 2013 Jun;7(4):452-61. doi: 10.3109/17435390.2012.674571. Epub 2012 Apr 4.
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.
采用体内和体外试验研究了多壁碳纳米管(MWCNTs)的遗传毒性作用。MWCNTs 可显著诱导 A549 细胞形成微核,并增强 CHO AA8 细胞姐妹染色单体交换(SCE)的频率。当 ICR 小鼠气管内单次注入 MWCNTs(0.05 或 0.2mg/动物)时,彗星试验分析的肺 DNA 损伤呈剂量依赖性增加。此外,MWCNT 暴露的小鼠肺中发生了 DNA 氧化损伤,由 8-氧-7,8-二氢-2'-脱氧鸟苷和庚酮乙氧基脱氧核苷酸表示。在经 MWCNT 处理的 gpt 缺失转基因小鼠的肺中,gpt 突变频率显著增加。转换是主要的,并且 MWCNTs 明显增加了 G:C 到 C:G 的转换。此外,在 MWCNT 暴露的小鼠肺中观察到许多区域经诱导型一氧化氮合酶和硝基酪氨酸免疫组织化学染色。总之,MWCNTs 在体内和体外试验中均显示出遗传毒性;其机制可能涉及氧化应激和炎症反应。