Finnish Institute of Occupational Health, Nanosafety Research Center, Helsinki, Finland.
Nanotoxicology. 2012 Dec;6:825-36. doi: 10.3109/17435390.2011.625130. Epub 2011 Oct 13.
We examined if three commercially available nanomaterials - short singlewall carbon nanotubes (SWCNTs), short multiwall carbon nanotubes (MWCNTs) and nanosized titanium dioxide anatase (TiO(2); primary particle size <25 nm) - can induce structural chromosomal aberrations (CAs) in cultures of isolated human lymphocytes. To find a suitable sampling time, the cells were treated with 6.25-300 μg/ml of the nanomaterials for 24, 48 and 72 h. The 48-h treatment was the most effective, inducing a dose-dependent increase in chromosome-type CAs (all materials) and chromatid-type CAs (SWCNTs and TiO(2) anatase). The 72-h treatment yielded a positive result with SWCNTs. None of the treatments significantly affected cell count or the mitotic index. Our results suggest that with nanomaterials a continuous treatment for about two cell cycles is needed for CA induction, possibly reflecting access of nanomaterials to the nucleus during the first mitosis or delayed secondary genotoxic effect associated with the inflammatory process.
我们研究了三种市售纳米材料——短单壁碳纳米管(SWCNTs)、短多壁碳纳米管(MWCNTs)和纳米级锐钛矿型二氧化钛(TiO2;初级粒径<25nm)——是否会在离体人淋巴细胞培养物中诱导结构染色体畸变(CAs)。为了找到合适的采样时间,用 6.25-300μg/ml 的纳米材料处理细胞 24、48 和 72 小时。48 小时的处理最为有效,诱导染色体型 CAs(所有材料)和染色单体型 CAs(SWCNTs 和 TiO2锐钛矿)呈剂量依赖性增加。SWCNTs 在 72 小时的处理中产生了阳性结果。没有一种处理方法显著影响细胞计数或有丝分裂指数。我们的结果表明,对于 CA 的诱导,纳米材料需要大约两个细胞周期的连续处理,这可能反映了纳米材料在第一次有丝分裂过程中进入细胞核,或者与炎症过程相关的延迟性二次遗传毒性效应。