Institute of Medical Microbiology, University Hospital Münster, 48149 Münster, Germany.
Biomolecules. 2022 Mar 3;12(3):395. doi: 10.3390/biom12030395.
Several methods to isolate monocytes from whole blood have been previously published, with different advantages and disadvantages. For the purpose of cytokine release assessment upon external stimulation, the use of monocyte preparations consisting of non-activated cells is prerequisite. Affinity-isolated monocyte preparations from peripheral blood mononuclear cells (PBMCs), obtained via positive or negative selection using magnetic beads, released pro-inflammatory cytokines such as TNF-α and IL-6 even without adding external stimuli, hindering any assessment of an effect of bacterial lipoproteins on cell stimulation. Hence, the cell preparation protocol was modified by adding a quiescence step on repellent surface culture plates, dampening any monocyte pre-activation. This protocol now provides a robust method to prepare silent yet fully activatable, pure monocyte populations for further use in stimulus-elicited activation experiments.
已经有几种从全血中分离单核细胞的方法被先前报道,它们各有优缺点。为了在外部刺激下评估细胞因子的释放,使用由非激活细胞组成的单核细胞制剂是前提。使用亲和磁珠通过正选或负选从外周血单个核细胞(PBMCs)中分离得到的单核细胞制剂,即使不添加外部刺激,也会释放 TNF-α和 IL-6 等促炎细胞因子,从而阻碍对细菌脂蛋白对细胞刺激作用的任何评估。因此,通过在排斥表面培养板上添加静止步骤来修改细胞制备方案,从而抑制任何单核细胞的预先激活。该方案现在提供了一种强大的方法来制备沉默但完全可激活的、纯的单核细胞群体,以供进一步用于刺激诱导的激活实验。