癌变·畸变·突变 ›› 2005, Vol. 17 ›› Issue (3): 171-174.doi: 10.3969/j.issn.1004-616x.2005.03.012

• 论著 • 上一篇    下一篇

微囊藻毒素Microcystin-LR体外遗传毒性

詹 立;张立实;王 莉;张 浩;朱 玲;铃木孝昌;本间正充;吴德生   

  1. 四川大学华西医院国家成都中药安全性评价中心,四川 成都 610041
  • 收稿日期:2005-01-17 修回日期:2005-03-06 出版日期:2005-05-30 发布日期:2005-05-30
  • 通讯作者: 吴德生

Genetic Toxicity Induced by Microcystin-LR in Vitro

ZHAN Li;ZHANG Li-shi; WANG Li;ZHANG Hao;ZHU Ling;TAKAYOSHI Suzuki; MASAMITSU Honma;WU De-sheng   

  1. National Chengdu Center for Safety Evaluation of Traditional Chinese Medicine, West China Hospital, Sichuan University, Chengdu 610041,Sichuan,China
  • Received:2005-01-17 Revised:2005-03-06 Online:2005-05-30 Published:2005-05-30
  • Contact: WU De-sheng

摘要: 背景与目的: 应用人类淋巴母细胞TK6研究微囊藻毒素 (Microcystin-LR,MCLR)的体外遗传毒性。 材料与方法: MCLR体外染毒TK6细胞4 h或24 h后检测细胞毒性、微核及tk位点突变频率。 结果: 4 h染毒未引发明显细胞毒性,24 h MCLR染毒导致TK6细胞相对存活率下降,细胞微核率及TK基因突变频率明显上升,并有剂量-反应关系。最高浓度组(80 μg/ml)的细胞微核率及TK基因突变频率分别是对照组的4.8及5.1倍。MCLR诱发tk位点两种不同表型的突变细胞集落,即正常生长集落及缓慢生长集落,并以后者为主。 结论: 24 h染毒MCLR可以诱发TK6细胞微核及基因突变,揭示MCLR可能是一种断裂剂。

关键词: 微囊藻毒素, 微核, 突变, TK6细胞

Abstract: BACKGROUND & AIM: Human lymphoblastoid cell line TK6 was used to investigate the in vitro genotoxicity of Microcystin-LR. MATERIAL AND METHODS: Cytotoxicity response, micronucleus(MN) and mutation frequency at tk locus induced by MCLR after 4 h or 24 h treatment were detected. RERULTS: Treatment with MCLR for 4 h did not induce a significant cytotoxic response at less than 80 μg/ml. Exposure to MCLR for 24h decreased relative survival(RS), induced both MN and TK mutation in a concentration-dependent manner. The maximum induction of MN and TK mutation were 4.8 and 5.1 times those of the control,respectively. Two distinct phenotypic colonies of TK mutants were generated , namely tk-NG and tk-SG mutant colonies but the latter dominated. CONCLUSION: MCLR was clastogenic in TK6 human lymphoblastoid cells .

Key words: Microcystin-LR, micronucleus, mutation, TK6 cell