Hardin J A, Downs J T
J Immunol Methods. 1981;40(1):1-6. doi: 10.1016/0022-1759(81)90074-0.
We have developed a rapid and simple method for isolating monocytes from peripheral blood. After mononuclear cells are isolated on a Ficoll-Hypaque gradient, the monocytes are purified by sedimentation for 5 min through a re-orienting gradient of Percoll. The method is easily reproducible and yields approximately half of the monocytes in staring blood, with minimal contamination by lymphocytes. Although both monocytes and lymphocytes have similar densities, separation occurs because these cells migrate at differing rates through the gradient to reach their equilibration point. The recovered monocytes are viable and functional; over 95% of them exclude trypan blue and they adhere to glass and plastic and ingest latex particles normally. By virtue of the rapidity and gentle nature of its centrifugation steps, the method exposes cells to only very limited non-physiologic conditions. For this reason and because the monocytes are maintained in suspension, opportunities for functional alterations are minimized.
我们已经开发出一种从外周血中分离单核细胞的快速简便方法。在通过Ficoll-泛影葡胺梯度分离出单核细胞后,单核细胞通过在Percoll重定向梯度中沉降5分钟来纯化。该方法易于重复,可获得起始血液中约一半的单核细胞,淋巴细胞污染极少。尽管单核细胞和淋巴细胞密度相似,但由于这些细胞通过梯度迁移的速率不同,以达到其平衡点,从而实现分离。回收的单核细胞具有活性且功能正常;超过95%的细胞能排斥台盼蓝,它们能正常地黏附于玻璃和塑料并摄取乳胶颗粒。由于其离心步骤快速且温和,该方法使细胞仅暴露于非常有限的非生理条件下。因此,并且由于单核细胞保持悬浮状态,功能改变的机会被最小化。