Wang Zheng, Zhang Tianbao, Zhu Yongfei, Zhu Jiangbo
Department of Toxicology, Second Military Medical University, Shanghai 200433, China.
Wei Sheng Yan Jiu. 2007 Jan;36(1):20-3.
To provide the proof for the high throughput screening method in vitro by establishing the comet assay in vitro using HepG2 cells plated in 96-well plates.
Plating HepG2 cells in 96-well plates, and then detecting the cytotoxicity using the neutral red method before comet assay.
8 genotoxicial agents could be detected using the method and the sensitivity was 100% , the ratio of the comet cells and the length of the tail of the comet were increased with the increasing dose when the cytotoxicity less than 50%. 11 non-genotoxicial agents could be detected within 12 non-genotoxicial agents and the specificity was 91%.
(1) This method could detect the direct genotoxic agents and the indirect genotoxic agents at the absent of the S9. (2)4-5 agents could be detected in the same 96-well plate using the method. (3) Using the method, we could obtain an dose at which the agent could cause genotoxicity. (4) By plating cells in plates in vitro, increased the speed of the detection and reduced the consumption of the agents. (5) The method could be developed into the high throughput screening method in vitro.
通过在96孔板中培养HepG2细胞建立体外彗星试验,为体外高通量筛选方法提供依据。
将HepG2细胞接种于96孔板,在彗星试验前用中性红法检测细胞毒性。
该方法可检测8种遗传毒性剂,灵敏度为100%,当细胞毒性小于50%时,彗星细胞比例和彗尾长度随剂量增加而增加。在12种非遗传毒性剂中可检测出11种,特异性为91%。
(1)该方法在无S9的情况下可检测直接遗传毒性剂和间接遗传毒性剂。(2)用该方法在同一96孔板中可检测4 - 5种试剂。(3)用该方法可获得试剂引起遗传毒性的剂量。(4)通过体外细胞接种,提高了检测速度,减少了试剂消耗。(5)该方法可发展成为体外高通量筛选方法。