Repnik Urska, Knezevic Miomir, Jeras Matjaz
Blood Transfusion Centre of Slovenia, Tissue Typing Centre, Slajmerjeva 6, 1000 Ljubljana, Slovenia.
J Immunol Methods. 2003 Jul;278(1-2):283-92. doi: 10.1016/s0022-1759(03)00231-x.
We have optimized the procedure of monocyte isolation on a Percoll density gradient. The new procedure consists of three steps: (1) the isolation of MNC on a Ficoll density gradient; (2) the separation of monocytes from lymphocytes on a high-density hyper-osmotic Percoll density gradient; and (3) the separation of monocytes from platelets and dead cells on a low-density iso-osmotic Percoll density gradient. The procedure is simple and cost-effective. Monocyte purity and recovery are both about 75% and platelet contamination is low. The isolated monocytes retain their capacity to differentiate into dendritic cells in vitro.
我们优化了在Percoll密度梯度上分离单核细胞的程序。新程序包括三个步骤:(1)在Ficoll密度梯度上分离单核细胞;(2)在高密度高渗Percoll密度梯度上从淋巴细胞中分离单核细胞;(3)在低密度等渗Percoll密度梯度上从血小板和死细胞中分离单核细胞。该程序简单且具有成本效益。单核细胞纯度和回收率均约为75%,血小板污染低。分离出的单核细胞在体外保留了分化为树突状细胞的能力。