Zhao Jimin, Ma Junfen, Zhao Jun, Yang Hongyan
Department of Pathophysiology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou 450052,China.
Wei Sheng Yan Jiu. 2009 Mar;38(2):133-5.
To study the cytotoxicity of altemariol (AOH) on NIH/3T3 cells.
Logarithmic growth phase NIH/3T3 cells were treated at the dose of 10 micromol/L and 50 micromol/L AOH as treatment groups and treated with DMSO (0.25%). The effects of AOH on cell proliferations were assessed by morphologic observasion. Inhibition rates of AOH were determined by MTT assay. Comet assay was used to examine DNA damage induced by AOH. Cell cycle distributions were detected by flow cytometric assay (FCM).
The cells treated with AOH occured morlogic changes. The inhibition rates of 10 micromol/L and 50 micromol/L AOH were 19.88% and 32.47% respectively. In the comet assay two treatment groups percentages of tailed cells were 35.87% and 71.83% respectively. The DNA contents of the tail were (36.18 +/- 18.6) and (51.3 +/- 21.6) respectively. These datas were more higher than those of the solvent control (P < 0.05). In comparison with the control group, the percents of G2/M and S phase cells were increased after treatment of 50.0 micromol/L AOH for 24h (P < 0.05).
AOH could have acute cytotoxic effects on NIH/3T3 cells and inhibite cell proliferation and cause DNA damage. High dose of AOH could induce cell cycle arrest in G2/M phase.
研究交链孢酚(AOH)对NIH/3T3细胞的细胞毒性。
将处于对数生长期的NIH/3T3细胞分为处理组,分别用10微摩尔/升和50微摩尔/升的AOH处理,并用二甲基亚砜(0.25%)处理作为对照。通过形态学观察评估AOH对细胞增殖的影响。采用MTT法测定AOH的抑制率。用彗星试验检测AOH诱导的DNA损伤。通过流式细胞术(FCM)检测细胞周期分布。
用AOH处理的细胞出现形态学变化。10微摩尔/升和50微摩尔/升AOH的抑制率分别为19.88%和32.47%。在彗星试验中,两个处理组的拖尾细胞百分比分别为35.87%和71.83%。尾部的DNA含量分别为(36.18±18.6)和(51.3±21.6)。这些数据均显著高于溶剂对照组(P<0.05)。与对照组相比,50.0微摩尔/升AOH处理24小时后,G2/M期和S期细胞百分比增加(P<0.05)。
AOH对NIH/3T3细胞具有急性细胞毒性作用,可抑制细胞增殖并导致DNA损伤。高剂量的AOH可诱导细胞周期阻滞于G2/M期。