Irimia Daniel
Massachusetts General Hospital, Harvard Medical School, and Shirners Hospitals for Children, Boston, Massachusetts, USA.
Methods Cell Biol. 2014;121:141-53. doi: 10.1016/B978-0-12-800281-0.00010-5.
We describe a protocol for measuring the speed of human neutrophils migrating through small channels, in conditions of mechanical confinement comparable to those experienced by neutrophils migrating through tissues. In such conditions, we find that neutrophils move persistently, at constant speed for tens of minutes, enabling precise measurements at single cells resolution, for large number of cells. The protocol relies on microfluidic devices with small channels in which a solution of chemoattractant and a suspension of isolated neutrophils are loaded in sequence. The migration of neutrophils can be observed for several hours, starting within minutes after loading the neutrophils in the devices. The protocol is divided into four main steps: the fabrication of the microfluidic devices, the separation of neutrophils from whole blood, the preparation of the assay and cell loading, and the analysis of data. We discuss the practical steps for the implementation of the migration assays in biology labs, the adaptation of the protocols to various cell types, including cancer cells, and the supplementary device features required for precise measurements of directionality and persistence during migration.
我们描述了一种用于测量人类中性粒细胞在小通道中迁移速度的实验方案,该实验条件下的机械限制与中性粒细胞在组织中迁移时所经历的条件相当。在这种条件下,我们发现中性粒细胞持续移动,以恒定速度移动数十分钟,从而能够在单细胞分辨率下对大量细胞进行精确测量。该实验方案依赖于具有小通道的微流控装置,在该装置中依次加载趋化因子溶液和分离的中性粒细胞悬浮液。中性粒细胞的迁移可以在将其加载到装置中几分钟后开始观察数小时。该实验方案分为四个主要步骤:微流控装置的制造、从全血中分离中性粒细胞、实验准备和细胞加载以及数据分析。我们讨论了在生物实验室中实施迁移实验的实际步骤、该实验方案对包括癌细胞在内的各种细胞类型的适应性,以及在迁移过程中精确测量方向性和持续性所需的辅助装置特征。