Handgretinger R, Welte B, Dopfer R, Niethammer D
Children's University Hospital, Tübingen, Germany.
J Clin Lab Anal. 1994;8(6):443-6. doi: 10.1002/jcla.1860080617.
A rapid method for the purification of CD56+ natural killer (NK) cells with the preferential enrichment of the CD56bright+ subset is described. The method is based on the adsorption of CD56+ cells indirectly stained with a biotinylated antibody on an avidin-coated column. The adsorbed CD56+ cells can then be squeezed out mechanically without damaging the viability or the function of the cells. Starting from peripheral mononuclear cells from adult donors, the recovery of the CD56+ cells was 11.9 +/- 9.0% (n = 8), the purity 93.0 +/- 4.9% (n = 10), and the enrichment factor 7.5 +/- 1.7 (n = 8). Further phenotypic classification of the CD56+ cells into CD56dim+ and CD56bright+ cells showed a preferential enrichment of the CD56bright+ phenotype with a recovery of 40.5 +/- 19.6% (n = 8), a purity of 30.3 +/- 13.2% (n = 8), and an enrichment factor of 29.8 +/- 7.2 (n = 8). In conclusion, the described method allows the rapid purification of CD56+ NK cells with the preferential enrichment of the CD56bright+ subset.
本文描述了一种快速纯化CD56+自然杀伤(NK)细胞的方法,该方法能优先富集CD56bright+亚群。该方法基于将用生物素化抗体间接染色的CD56+细胞吸附在抗生物素蛋白包被的柱上。然后可以机械挤出吸附的CD56+细胞,而不会损害细胞的活力或功能。从成年供体的外周单核细胞开始,CD56+细胞的回收率为11.9±9.0%(n = 8),纯度为93.0±4.9%(n = 10),富集因子为7.5±1.7(n = 8)。将CD56+细胞进一步表型分类为CD56dim+和CD56bright+细胞,结果显示CD56bright+表型优先富集,回收率为40.5±19.6%(n = 8),纯度为30.3±13.2%(n = 8),富集因子为29.8±7.2(n = 8)。总之,所述方法能够快速纯化CD56+NK细胞,并优先富集CD56bright+亚群。