癌变·畸变·突变 ›› 2007, Vol. 19 ›› Issue (6): 457-459.doi: 10.3969/j.issn.1004-616x.2007.06.008

• 论著 • 上一篇    下一篇

PBDE_47对人神经母细胞瘤SH_SY5Y细胞致突变作用

徐八一 /何卫红 /何 平 /夏 涛 /陈学敏 /王爱国   

  1. 华中科技大学同济医学院公共卫生学院劳动卫生与环境卫生学系
  • 收稿日期:2007-01-29 修回日期:2007-05-17 出版日期:2007-11-30 发布日期:2007-11-30
  • 通讯作者: 王爱国

Assessment of Mutagenicity of PBDE_47 in Human Neurobla_stoma SH_SY5Y Cells in Vitro

XU Ba-yi, HE Wei-hong, HE Ping, XIA Tao,CHEN Xue-min,WANG Ai-guo   

  1. MOE Key Lab of Environment and Health, Department of Occupational & Environmental Health,School of Public Health,Tongji Medical College,Huazhong University of Science & Technology
  • Received:2007-01-29 Revised:2007-05-17 Online:2007-11-30 Published:2007-11-30
  • Contact: WANG Ai-guo

摘要: 背景与目的: 探讨2,2',4,4'_四溴联苯醚(2,2',4,4'_tetrabromodiphenyl ethers, PBDE_47)对人神经母细胞瘤SH_SY5Y细胞的致突变作用。 材料与方法: 设空白对照组、溶剂对照组、3个不同BDE_47剂量的试验组(1 μg、2 μg、4 μg/ml)和阳性对照组(MMC),共6组。SH_SY5Y细胞分别暴露于各组不同受试物24 h后,采用胞质分裂阻断法测定微核率、核浆桥率。 结果: PBDE_47可诱导SH_SY5Y细胞核分裂指数呈剂量依赖性下降,微核细胞率和核浆桥率呈剂量依赖性增加;2 μg/ml和4 μg/ml的染毒剂量可引起SH_SY5Y细胞核分裂指数明显降低(P<0.05)以及微核细胞率和核浆桥率的明显增加(P<0.05),而仅在4 μg/ml PBDE_47染毒组发现微核率明显增加(P<0.05)。 结论: PBDE_47可诱导SH_SY5Y细胞微核和核浆桥的形成,具有致突变作用。

关键词: PBDE_47, 致突变, 微核, 核浆桥

Abstract: BACKGROUND & AIM: To study the mutagenicity of 2,2',4,4'_tetrabromodiphenyl ethers (PBDE_47) in human neuroblastoma SH_SY5Y cells in vitro. MATERIALS AND METHODS: The frequencies of micronuclei(MNi) and nucleoplasmic bridges (NPBs) were measured after SH_SY5Y cells were exposed to different doses of PBDE_47 for 24 h in vitro. RESULTS: PBDE_47 caused a significant concentration_dependent decrease in nuclear division index(NDI), and a concentration_dependent increase in MNi frequency in terms of total MNi/1000 binucleated cells (BNCs), BNCs with MNi/1000 BNCs, and NPBs/1000 BNCs. The NDI was obviously decreased, while the frequencies of BNCs with MNi/1000 BNCs and NPBs/1000 BNCs were increased significantly at 2 μg/ml and above PBDE_47 _treated groups (P<0.05). There was statistically difference in frequcency of MNi/1000 BNCs only in 4 μg/ml PBDE_47_treated group (P<0.05). CONCLUSION: PBDE_47 may induce the MNi and NPB formation, causing mutagenicity.

Key words: PBDE_47, mutagenicity, micronuclei, nucleoplasmic bridges