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雷腊梅, 宋立荣. 微囊藻毒素LR诱导细胞毒性机制研究的细胞模型建立[J]. 水生生物学报, 2006, 30(4): 408-412.
引用本文: 雷腊梅, 宋立荣. 微囊藻毒素LR诱导细胞毒性机制研究的细胞模型建立[J]. 水生生物学报, 2006, 30(4): 408-412.
LEI La-Mei, SONG Li-Rong. ESTABLISHMENT OF CELL MODEL FOR THE STUDY OF CYTOTOXICITY INDUCED BY MICROCYSTIN-LR[J]. ACTA HYDROBIOLOGICA SINICA, 2006, 30(4): 408-412.
Citation: LEI La-Mei, SONG Li-Rong. ESTABLISHMENT OF CELL MODEL FOR THE STUDY OF CYTOTOXICITY INDUCED BY MICROCYSTIN-LR[J]. ACTA HYDROBIOLOGICA SINICA, 2006, 30(4): 408-412.

微囊藻毒素LR诱导细胞毒性机制研究的细胞模型建立

ESTABLISHMENT OF CELL MODEL FOR THE STUDY OF CYTOTOXICITY INDUCED BY MICROCYSTIN-LR

  • 摘要: 以18种细胞系为材料,研究微囊藻毒素LR(20μg/mL和50μg/mL)所诱导的细胞毒性。形态观察表明,在经过30h以上的微囊藻毒素处理后,PC-3,J82,786-0,5637,VERO-E6等5种细胞出现了明显的细胞形态改变,毒素浓度越高,形态改变越厉害。微囊藻毒素LR的细胞毒性用LDH泄漏来表示。结果显示,5种毒素处理细胞的LDH泄漏呈剂量依赖性增加,其中5637和PC-3的LDH泄漏在同样的处理后较为厉害;同对照比较,SOD活力在20μg/mL MCLR处理下呈增加趋势,但在50μg/mL浓度下则下降;GSH含量在两种浓度处理下呈总体下降趋势。鉴于对微囊藻毒素敏感性差异分析,作者选择以5637细胞为基础,建立微囊藻毒素的毒理机制研究模型。

     

    Abstract: Microcystins are a group of closely related cyclic heptapeptides produced by a variety of common cyanobacteria.These toxins cause hepatocyte damage by inhibiting protein phosphastases 1 and 2A, resulting in hyperphosphorylation of a number of different proteins.Furthermore, high incidence of primary liver cancer in Qidong and Haimen in China has been associated with bloom contaminated drinking water.The mechanisms of MC-induced hepatotoxicity and tumor promotion activity have not been fully elucidated.In this study, Using 18 cell lines as materials, the cytotoxicity induced by different concentrations of microcystin-LR (20 and 50Lg/mL-was studied.The morphological observation showed that five cell lines ( PC-3, J82, 786-O, 5637 and VERO-E6-underwent obviouslymorphological changes after 30h treatment with microcystin-LR ( MCLR-with a dose-dependent manner.The cytoxicity of MCLR was determined by LDH leakage that showed a dose-dependent increase in five cell lines treated with MCLR, of which LDH leakage for 5637 and PC-3 were more serious under the same treatment.The SOD activity for five cell lines tended to increase in 20Lg/mL MCLR treatment but sharply decrease in 50Lg/mL MCLR treatment compared with the control cells; the GSH content decreased totally in different treatment.Based on the analysis of the sensitivity discrepancy for MCLR, 5637 cell lines was chosen for the establishment of a cell model for the study of cytotoxicity induced by microcystin-LR.

     

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