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首页> 外文期刊>Image analysis and stereology >CYTOKINESIS-BLOCK MICRONUCLEUS ASSAY IN HUMAN GLIOMA CELLS EXPOSED TO RADIATION
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CYTOKINESIS-BLOCK MICRONUCLEUS ASSAY IN HUMAN GLIOMA CELLS EXPOSED TO RADIATION

机译:暴露于辐射的人胶质瘤细胞中的细胞因子阻滞微核检测

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Biological tests are efficient in reflecting the biological influences of several types of generally harmful exposures. The micronucleus assay is widely used in genotoxicity studies or studies on genomic damage in general. We present methodological aspects of cytokinesis-block micronucleus assay performed in human gliomas irradiated in vitro. Eight human glioblastoma cell lines obtained from DSMZ (Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH, Germany) were gamma-irradiated (60Co) over a dose range of 0-10 Gy. Cytokinesis-block micronucleus assay was performed to quantitate cytogenetic damage. The cells were fixed directly on dishes, stained with fluorochrome DAPI and evaluated under fluorescent and phase contrast microscope. The micronucleus frequency was expressed as a micronuclei (MN) per binucleated cell (BNC) ratio, calculated after scoring at least 100 BNC per dish. The frequency of spontaneous MN ranged from 0.17 to 0.613 (mean: 0.29 ± 0.14). After irradiation increase of MN frequency in the range of 0.312 - 2.241 (mean: 0.98 ± 0.68) was found at 10 Gy. Gliomas are extremely heterogenous in regard to cytogenetic effects of irradiation, as shown in this study by cytokinesis-block micronucleus assay. This test is easily performed on irradiated glioma cell lines and can assist in determining their radiosensitivity. However, in order to obtain reliable and reproducible results, precise criteria for MN scoring must be strictly followed. Simultaneous use of fluorescent and phase contrast equipment improves imaging of morphological details and can further optimize MN scoring.
机译:生物测试可以有效地反映几种类型的一般有害接触的生物影响。通常,微核分析广泛用于基因毒性研究或基因组损伤研究。我们目前在体外照射的人脑胶质瘤中进行的胞质分裂阻滞微核分析的方法学方面。在0-10 Gy的剂量范围内,对从DSMZ(Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH,德国)获得的八种人胶质母细胞瘤细胞系进行了γ射线辐照(60Co)。进行胞质分裂阻滞微核测定以定量细胞遗传学损伤。将细胞直接固定在培养皿上,用荧光染料DAPI染色,并在荧光和相差显微镜下进行评估。微核频率表示为每个双核细胞(BNC)的微核(MN)比,是在每个培养皿中至少获得100个BNC得分后计算的。自发性MN的频率范围为0.17至0.613(平均值:0.29±0.14)。辐照后,在10 Gy处发现MN频率增加了0.312-2.241(平均值:0.98±0.68)。正如本研究通过胞质分裂阻滞微核试验所显示的那样,胶质瘤在辐射的细胞遗传学效应方面极为不同。这项测试很容易在放射神经胶质瘤细胞系上进行,并且可以帮助确定它们的放射敏感性。但是,为了获得可靠和可重复的结果,必须严格遵循MN评分的精确标准。同时使用荧光和相衬设备可改善形态学细节的成像,并可进一步优化MN评分。

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