Neri S, Mariani E, Meneghetti A, Cattini L, Facchini A
Dipartimento di Medicina Interna e Gastroenterologia, University of Bologna, Bologna, Italy.
Clin Diagn Lab Immunol. 2001 Nov;8(6):1131-5. doi: 10.1128/CDLI.8.6.1131-1135.2001.
Cytotoxicity assays provide an in vitro evaluation of the lytic activity of NK and T cells against tumors or transformed cells. However, none of these methods allow the recovery of cells or supernatants after the assay. We standardized a microcytotoxicity test using calcein-acetoxymethyl (calcein-AM) dye that requires very small quantities of cells while maintaining the same sensitivity as the traditional (51)Cr assay. The assay is applicable to resting as well as activated human effector cells and uses different targets such as human cell lines that are adherent or growing in suspension and resistant or sensitive. The most important feature of the method is the possibility of recovering cells and supernatants for additional analyses such as phenotyping and evaluation of soluble factors.
细胞毒性测定提供了自然杀伤细胞(NK)和T细胞对肿瘤或转化细胞的裂解活性的体外评估。然而,这些方法都无法在测定后回收细胞或上清液。我们使用乙酰氧基甲基钙黄绿素(calcein-AM)染料标准化了一种微细胞毒性试验,该试验所需细胞量极少,同时保持与传统(51)铬测定相同的灵敏度。该测定适用于静息和活化的人类效应细胞,并使用不同的靶标,如贴壁生长或悬浮生长、耐药或敏感的人类细胞系。该方法最重要的特点是能够回收细胞和上清液,用于进一步分析,如细胞表型分析和可溶性因子评估。