癌变·畸变·突变 ›› 2008, Vol. 20 ›› Issue (4): 299-302.doi: 10.3969/j.issn.1004-616x.2008.04.013

• 论著 • 上一篇    下一篇

三丁基锡引起人羊膜细胞氧化损伤及DNA损伤的研究

朱 欣1/ 徐立红2   

  1. 1. 浙江省肿瘤医院肿瘤研究所,杭州 310022;2. 浙江大学医学院生物化学与遗传系,杭州 310058
  • 收稿日期:2007-11-20 修回日期:2007-12-11 出版日期:2008-07-30 发布日期:2008-07-30

Study of Oxidative Damage and DNA Damage in FL Cells Induced by Tributyltin

ZHU Xin1, XU Li_hong2   

  1. 1. Zhejiang Cancer Research Institute, Zhejiang Cancer Hospital, Hangzhou 310022; 2. Department of Biochemistry and Genetics, School of Medicine, Zhejiang University,Hangzhou 310022,China
  • Received:2007-11-20 Revised:2007-12-11 Online:2008-07-30 Published:2008-07-30

摘要: 背景与目的: 研究三丁基锡 (tributyltin,TBT)对人羊膜细胞FL (human amnion cells) 氧化损伤和DNA损伤的诱导作用。 材料与方法: 将不同浓度TBT (0、2、4、6、8、10 μmol/L),分别对FL染毒2 h和4 h,各染毒组同时设不加TBT的对照组,染毒后分别用MTT法检测TBT对FL细胞增殖率的影响,用DCFH_DA法检测FL细胞活性氧自由基 (ROS)水平,用彗星实验检测TBT对FL细胞DNA的损伤。 结果: TBT对FL细胞染毒4 h时,其2、8、10 μmol/L浓度组的细胞增殖率较对照组显著下降(P<0.05,P<0.01,P<0.001),且随TBT浓度升高而增殖率呈下降的趋势。TBT 3、4 μmol/L染毒组FL细胞的ROS水平较对照组升高,且4 μmol/L染毒组与对照组比较差异具有统计学意义(P<0.05)。在TBT 2、3、4 μmol/L染毒组随着TBT浓度的升高,FL细胞核尾长、尾相均显著升高(P均<0.05)。 结论: TBT可引起FL细胞的氧化损伤及DNA损伤。

关键词: 三丁基锡, 氧化损伤, DNA损伤, 细胞凋亡

Abstract: BACKGROUND AND AIM: The study was undertaken to assess the oxidative stress and DNA damage in human amnion cells induced by TBT. MATERIALS AND METHODS: Cultured FL cells were exposed to different concentrations of TBT (0, 2, 4, 6, 8, 10 μmol/L) for different durations (2 h and 4 h). Cell proliferation rate was evaluated by MTT assay. After exposure to different concentrations of TBT (0,1,2,3,4 μmol/L) for 2 h,the ROS level and DNA damage of FL cells were measured by DCFH_DA method and the single cell gel electrophoresis method, respectively. RESULTS: After exposure to different concentrations of TBT for 4 h, the FL cell proliferation rates in the 2, 8, 10 μmol/L groups were significantly decreased as compared to control(P<0.05, P<0.01, P<0.001) in a dose_dependent manner. The ROS level was increased in the 3 and 4 μmol/L groups in the dose_dependent manner and the difference was significant at 4 μmol/L group compared to the control(P<0.05). Meanwhile, TBT exposure led to the interrelated increase of nucleus tail length and tail moment in a dose-dependent manner and the differences were significant at 2, 3 and 4 μmol/L group compared to the control(P<0.05). CONCLUSION: TBT exposure could cause oxidative stress and DNA damage to FL cells.

Key words: tributyltin, oxidative damage, DNA damage, apoptosis