George Jiya M, Magogotya Millicent, Vetten Melissa A, Buys Antoinette V, Gulumian Mary
Toxicology and Biochemistry Department, National Institute for Occupational Health, Johannesburg 2000, Gauteng, South Africa.
Department of Biotechnology and Food Technology, Tshwane University of Technology, Nelson Mandela Drive, Private Bag X680, Pretoria 0001, South Africa.
Toxicol Sci. 2017 Mar 1;156(1):149-166. doi: 10.1093/toxsci/kfw247.
The suitability of 4 in vitro assays, commonly used for mutagenicity and genotoxicity assessment, was investigated in relation to treatment with 14 nm citrate-stabilized gold nanoparticles (AuNPs). Specifically, the Ames test was conducted without metabolic activation, where no mutagenic effects were observed. High resolution transmission electron microscopy and Cytoviva dark-field image analysis showed that AuNPs did not enter the bacterial cells, thus confirming the unreliability of the Ames test for nanoparticle mutagenicity studies. In addition, the Chinese hamster ovary (CHO) cell line was used for Comet, Chromosome aberration and Micronucleus assays. CHO cells were treated with AuNPs for 20 h at 37 °C. Cytotoxicity was not detected by cell impedance studies even though AuNP uptake was confirmed using Cytoviva image analysis. The DNA damage was statistically significant in treated cells when assessed by the Comet assay. However, minimal and nonstatistically significant chromosomal DNA damage was observed using the chromosome aberration and micronucleus assays. In this study, we showed that false positive results obtained with Comet assay may have been due to the possibility of direct contact between the residual, intracellular AuNPs and DNA during the assay procedure. Therefore, the chromosome aberration and micronucleus assays are better suited to assess the genotoxic effects of nanoparticles due to low probability of such direct contact occurring. Genotoxic effect of 14 and 20 nm citrate-stabilized, as well as, 14 nm PCOOH AuNPs were also investigated using chromosome aberration and micronucleus assays. Based on our acceptance criteria for a positive genotoxic response, none of the AuNPs were found to be genotoxic in either of these assays.
研究了常用于致突变性和遗传毒性评估的4种体外试验方法对于用14纳米柠檬酸盐稳定的金纳米颗粒(AuNP)处理的适用性。具体而言,在没有代谢活化的情况下进行了艾姆斯试验,未观察到致突变作用。高分辨率透射电子显微镜和Cytoviva暗场图像分析表明,AuNP未进入细菌细胞,从而证实了艾姆斯试验在纳米颗粒致突变性研究中的不可靠性。此外,中国仓鼠卵巢(CHO)细胞系用于彗星试验、染色体畸变试验和微核试验。CHO细胞在37℃下用AuNP处理20小时。尽管使用Cytoviva图像分析确认了AuNP的摄取,但细胞阻抗研究未检测到细胞毒性。通过彗星试验评估时,处理过的细胞中的DNA损伤具有统计学意义。然而,使用染色体畸变试验和微核试验观察到的染色体DNA损伤最小且无统计学意义。在本研究中,我们表明彗星试验获得的假阳性结果可能是由于在试验过程中残留的细胞内AuNP与DNA之间直接接触的可能性。因此,染色体畸变试验和微核试验更适合评估纳米颗粒的遗传毒性作用,因为这种直接接触发生的可能性较低。还使用染色体畸变试验和微核试验研究了14纳米和20纳米柠檬酸盐稳定的以及14纳米PCOOH AuNP的遗传毒性作用。根据我们对阳性遗传毒性反应的接受标准,在这些试验中均未发现任何AuNP具有遗传毒性。