Eastmond D A, Tucker J D
Biomedical Sciences Division, Lawrence Livermore National Laboratory, CA 94550.
Mutat Res. 1989 Dec;224(4):517-25. doi: 10.1016/0165-1218(89)90079-7.
We have developed a modified micronucleus assay using an antikinetochore antibody and cytokinesis-blocked Chinese hamster ovary cells as a simple and rapid method for detecting aneuploidy-inducing agents. The presence of a kinetochore in a micronucleus of a binucleated cell indicates a cell with a high probability for aneuploidy following cytokinesis. The method requires minimal training to perform and score and can readily distinguish aneuploidy-inducing agents from clastogens. Micronucleated cells treated with the aneuploidy-inducing agents benomyl and vinblastine sulfate contained a kinetochore-positive micronucleus 92% and 94% of the time whereas micronucleated cells treated with the clastogen methyl methanesulfonate contained a kinetochore-positive micronucleus only 11% of the time. This relatively simple method for distinguishing aneuploidy-inducing agents from clastogenic agents may be used as a routine genotoxicity assay to identify environmental and therapeutic agents with aneuploidy-inducing properties.
我们开发了一种改良的微核试验,使用抗动粒抗体和胞质分裂阻滞的中国仓鼠卵巢细胞,作为检测非整倍体诱导剂的简单快速方法。双核细胞微核中存在动粒表明该细胞在胞质分裂后产生非整倍体的可能性很高。该方法在操作和评分方面所需的培训极少,并且能够轻松区分非整倍体诱导剂和断裂剂。用非整倍体诱导剂苯菌灵和硫酸长春碱处理的微核细胞,分别有92%和94%的时间含有动粒阳性微核,而用断裂剂甲磺酸甲酯处理的微核细胞,只有11%的时间含有动粒阳性微核。这种区分非整倍体诱导剂和断裂剂的相对简单的方法,可用作常规遗传毒性试验,以鉴定具有非整倍体诱导特性的环境和治疗药物。