Hussain R F, Nouri A M, Oliver R T
Department of Medical Oncology, Royal London Hospital, UK.
J Immunol Methods. 1993 Mar 15;160(1):89-96. doi: 10.1016/0022-1759(93)90012-v.
Using in vitro established tumour cell lines attempts were made to assess the suitability of tetrazolium salt reduction (MTT) assay to replace the conventional radioactive base techniques for measuring cell proliferation and cell killing. The optimum conditions for MTT loading time, concentration of MTT and the time for colour development were found to be 4 h, 5 mg/ml and 30 min respectively, conditions which were used for subsequent experiments. Analysis of the correlation between increasing cell numbers and optical densities (OD) showed a direct relationship with correlation of coefficient values of r > 0.98 and 10,000 cells/well was found to provide an accurate ODs for a wide variety of cell types. The accuracy of replicate readings of the assay was investigated by setting a wide range of cell numbers and the variation among seven replicates was calculated and found to be less that 6% of the mean values. The reproducibility of the assay for two cell lines was tested using the lines on four different occasions. The ODs for Jar and Fen cell lines were 0.80 +/- 0.01, 0.82 +/- 0.02, 0.90 +/- 0.02, 0.79 +/- 0.05 and 0.56 +/- 0.01, 0.58 +/- 0.03, 0.60 +/- 0.02 and 0.61 +/- 0.02 respectively giving maximum variation of less than 11% of mean on repeated testings. Comparison between the results of MTT with 3H-Tdr or 51Cr release assays showed a high degree of correlation over a wide range of cell numbers and cell types. The r values between the results of MTT with 3H-Tdr (for cell number ranging from 1.8 to 60 x 10(3)/well) or 51Cr release assays (for E/T ratios of between 5:1 and 40:1) were 0.89 (p = 0.001) and 0.96 (p < 0.03) respectively. These results demonstrate that it is possible to use the MTT assay interchangeably with radioactive base techniques to measure cell proliferation and cytotoxicity. The ease of its execution, safety and its suitability for analysing as few as 3000 cells makes this method a serious contender for replacing the conventional radioactive techniques.
利用体外建立的肿瘤细胞系,尝试评估四氮唑盐还原(MTT)法替代传统放射性碱基技术来测量细胞增殖和细胞杀伤的适用性。发现MTT加载时间、MTT浓度和显色时间的最佳条件分别为4小时、5毫克/毫升和30分钟,后续实验采用这些条件。对细胞数量增加与光密度(OD)之间的相关性分析表明,二者呈直接关系,相关系数r>0.98,并且发现每孔接种10,000个细胞可为多种细胞类型提供准确的OD值。通过设置广泛的细胞数量来研究该检测方法重复读数的准确性,并计算七个重复样本之间的变异,发现变异小于平均值的6%。使用两种细胞系在四个不同时间点进行检测,以测试该检测方法的可重复性。Jar和Fen细胞系的OD值分别为0.80±0.01、0.82±0.02、0.90±0.02、0.79±0.05和0.56±0.01、0.58±0.03、0.60±0.02和0.61±0.02,重复检测时的最大变异小于平均值的11%。MTT结果与3H-Tdr或51Cr释放检测结果之间的比较表明,在广泛的细胞数量和细胞类型范围内具有高度相关性。MTT结果与3H-Tdr(细胞数量范围为1.8至60×10³/孔)或51Cr释放检测(E/T比在5:1至40:1之间)的r值分别为0.89(p = 0.001)和0.96(p < 0.03)。这些结果表明,MTT法可以与放射性碱基技术互换使用来测量细胞增殖和细胞毒性。该方法操作简便、安全,适用于分析低至3000个细胞,使其成为替代传统放射性技术的有力竞争者。