Nociari M M, Shalev A, Benias P, Russo C
Division of Geriatrics, Cornell University Medical College, New York, NY 10021, USA.
J Immunol Methods. 1998 Apr 15;213(2):157-67. doi: 10.1016/s0022-1759(98)00028-3.
In this study, a fluorometric method using alamarBlue has been developed for detecting cell-mediated cytotoxicity in vitro. AlamarBlue is a non-toxic metabolic indicator of viable cells that becomes fluorescent upon mitochondrial reduction. Specific lysis of targets by effector cells is quantified by comparing the total number of viable cells in wells containing effector and targets together, with wells where target and effector cells were separately seeded. Cell-mediated cytotoxic activity by alloreactive T cells and natural killer cells has been detected using a novel application of the alamarBlue technique. The assay that we have developed to detect cell-mediated cytotoxicity is extremely sensitive and specific and requires a significant lower number of effector cells than the standard 51Cr assay. Since alamarBlue reagent is non-toxic to cells and the assay can be performed under sterile conditions, effector cells may be recovered at the end for further analysis or cell expansion, if desired. Direct comparison of cell-mediated cytotoxicity measured by the alamarBlue method with the standard 51Cr release assay revealed that the former method is as specific and more sensitive than the conventional assay. Moreover, very small inter and intra-assay variations have been observed for alamarBlue cytotoxicity assays. In conclusion, this study shows that the alamarBlue assay is an extremely sensitive, economical, simple and non-toxic procedure to evaluate cell-mediated cytotoxicity that yields accurate results using a limited number of effector cells. Furthermore, since this assay is a one-step procedure, and does not involve any risk for the personnel, it may be useful to analyze automatically cell-mediated cytotoxicity in a large number of samples.
在本研究中,已开发出一种使用alamarBlue的荧光法来检测体外细胞介导的细胞毒性。alamarBlue是一种对活细胞无毒的代谢指示剂,在线粒体还原时会发出荧光。通过比较含有效应细胞和靶细胞的孔中活细胞总数与分别接种靶细胞和效应细胞的孔中活细胞总数,来量化效应细胞对靶标的特异性裂解。使用alamarBlue技术的新应用检测了同种异体反应性T细胞和自然杀伤细胞的细胞介导的细胞毒性活性。我们开发的用于检测细胞介导的细胞毒性的检测方法极其灵敏且特异,与标准的51Cr检测相比,所需的效应细胞数量要少得多。由于alamarBlue试剂对细胞无毒,且该检测可在无菌条件下进行,如有需要,可在最后回收效应细胞以进行进一步分析或细胞扩增。将alamarBlue方法测得的细胞介导的细胞毒性与标准的51Cr释放检测直接比较表明,前一种方法与传统检测一样特异且更灵敏。此外,alamarBlue细胞毒性检测的批间和批内变异非常小。总之,本研究表明,alamarBlue检测是一种极其灵敏、经济、简单且无毒的评估细胞介导的细胞毒性的方法,使用有限数量的效应细胞就能得出准确结果。此外,由于该检测是一步法,且对人员没有任何风险,因此可能有助于自动分析大量样品中的细胞介导的细胞毒性。