Timonen T, Reynolds C W, Ortaldo J R, Herberman R B
J Immunol Methods. 1982;51(3):269-77. doi: 10.1016/0022-1759(82)90393-3.
We describe a method for the purification of human and rat large granular lymphocytes (LGL), which are known to be the mediators of natural killer (NK) activity in these species. Plastic non-adherent and nylon wool passed blood mononuclear cells were separated into 7 fractions by discontinuous density gradient centrifugation on Percoll. Low density cells were highly enriched in LGL (up to 85% purity), whereas high density cells were typical small and medium sized lymphocytes devoid of NK activity. Human LGL could further be enriched by depleting high affinity sheep erythrocyte rosette-forming cells from the LGL-enriched Percoll fractions (resulting in up to greater than 90% purity). One critical variable in the separation technique was osmolarity, since the separation did not work optimally, if 290 mOsmoles/kg H2O in the Percoll solution was exceeded.
我们描述了一种纯化人及大鼠大颗粒淋巴细胞(LGL)的方法,已知这些细胞是这些物种中自然杀伤(NK)活性的介质。通过在Percoll上进行不连续密度梯度离心,将塑料非贴壁和尼龙毛柱通过的血液单核细胞分离为7个组分。低密度细胞高度富含LGL(纯度高达85%),而高密度细胞是典型的无NK活性的中小型淋巴细胞。通过从富含LGL的Percoll组分中去除高亲和力绵羊红细胞花环形成细胞,人LGL可进一步富集(纯度高达90%以上)。分离技术中的一个关键变量是渗透压,因为如果Percoll溶液中的渗透压超过290毫渗摩尔/千克H2O,分离效果就不会最佳。