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Genotoxicity of microcystin-LR in human lymphoblastoid TK6 cells.

机译:微囊藻毒素-LR对人淋巴母细胞TK6细胞的遗传毒性。

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摘要

Toxic cyanobacteria (blue-green algae) water blooms have become a serious problem in several industrialized areas of the world. Microcystin-LR (MCLR) is a cyclic heptapeptidic toxin produced by the cyanobacteria. In the present study, we used human lymphoblastoid cell line TK6 to investigate the in vitro genotoxicity of MCLR. In a standard 4h treatment, MCLR did not induce a significant cytotoxic response at <80 microg/ml. In a prolonged 24h treatment, in contrast, it induced cytotoxic as well as mutagenic responses concentration-dependently starting at 20 microg/ml. At the maximum concentration (80 microg/ml), the micronucleus frequency and the mutation frequency at the heterozygous thymidine kinase (TK) locus were approximately five-times the control values. Molecular analysis of the TK mutants revealed that MCLR specifically induced loss of heterozygosity at the TK locus, but not point mutations or other small structural changes. These results indicate that MCLR had a clastogenic effect. We discuss the mechanisms of MCLR genotoxicity and the possibility of its being a hepatocarcinogen.
机译:在世界上几个工业化地区,有毒的蓝细菌(蓝藻)水华已经成为一个严重的问题。微囊藻毒素-LR(MCLR)是由蓝细菌产生的环状七肽毒素。在本研究中,我们使用人类淋巴母细胞系TK6来研究MCLR的体外遗传毒性。在标准的4h处理中,MCLR在<80 microg / ml时不会诱导明显的细胞毒性反应。相反,在延长的24h处理中,它从20 microg / ml起浓度依赖性地诱导了细胞毒性以及诱变反应。在最大浓度(80微克/毫升)下,杂合胸苷激酶(TK)基因座的微核频率和突变频率约为对照值的五倍。对TK突变体的分子分析表明,MCLR特异性地诱导了TK基因位点杂合性的丧失,但不是点突变或其他小的结构变化。这些结果表明MCLR具有成胶作用。我们讨论了MCLR遗传毒性的机制及其成为肝致癌物的可能性。

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