Neville M E
J Immunol Methods. 1987 May 4;99(1):77-82. doi: 10.1016/0022-1759(87)90034-2.
This report describes a sensitive and reproducible cytotoxicity assay which is ideal for screening toxic compounds or soluble lytic factors from leukocytes. The assay relies on the ability of sodium [51Cr]chromate to be taken up by viable but not dead cells. This assay is the reverse of the conventional 51Cr-release assay. The target cells are 51Cr-labeled after incubation with cytotoxic factors. 51Cr-uptake does not depend on DNA, RNA or protein synthesis and the only parameters which influence its uptake are temperature, viability, number and cell volume.
本报告描述了一种灵敏且可重复的细胞毒性检测方法,该方法非常适合筛选有毒化合物或白细胞中的可溶性溶解因子。该检测方法依赖于[51Cr]铬酸钠被活细胞而非死细胞摄取的能力。此检测方法与传统的51Cr释放检测方法相反。在与细胞毒性因子孵育后,靶细胞被51Cr标记。51Cr摄取不依赖于DNA、RNA或蛋白质合成,影响其摄取的唯一参数是温度、活力、数量和细胞体积。