Najmeh Sara, Cools-Lartigue Jonathan, Giannias Betty, Spicer Jonathan, Ferri Lorenzo E
LD MacLean Surgical Research Laboratories, Department of Surgery, McGill University;
LD MacLean Surgical Research Laboratories, Department of Surgery, McGill University.
J Vis Exp. 2015 Apr 16(98):52687. doi: 10.3791/52687.
Neutrophil Extracellular Traps (NETs) have been recently identified as part of the neutrophil's antimicrobial armamentarium. Apart from their role in fighting infections, recent research has demonstrated that they may be involved in many other disease processes, including cancer progression. Isolating purified NETs is a crucial element to allow the study of these functions. In this video, we demonstrate a simplified method of cell free NET isolation from human whole blood using readily available reagents. Isolated NETs can then be used for immunofluorescence staining, blotting or various functional assays. This enables an assessment of their biologic properties in the absence of the potential confounding effects of neutrophils themselves. A density gradient separation technique is employed to isolate neutrophils from healthy donor whole blood. Isolated neutrophils are then stimulated by phorbol 12-myristate 13-acetate (PMA) to induce NETosis. Activated neutrophils are then discarded, and a cell-free NET stock is obtained. We then demonstrate how isolated NETs can be used in an adhesion assay with A549 human lung cancer cells. The NET stock is used to coat the wells of a 96 well cell culture plate O/N, and after ensuring an adequate NET monolayer formation on the bottom of the wells, CFSE labeled A549 cells are added. Adherent cells are quantified using a Nikon TE300 fluorescent microscope. In some wells, 1000U DNAse1 is added 10 min before counting to degrade NETs.
中性粒细胞胞外陷阱(NETs)最近被确认为中性粒细胞抗菌武器库的一部分。除了在对抗感染中的作用外,最近的研究表明它们可能参与许多其他疾病过程,包括癌症进展。分离纯化的NETs是研究这些功能的关键要素。在本视频中,我们展示了一种使用现成试剂从人全血中分离无细胞NETs的简化方法。然后,分离出的NETs可用于免疫荧光染色、印迹或各种功能测定。这使得在没有中性粒细胞自身潜在混杂效应的情况下评估它们的生物学特性成为可能。采用密度梯度分离技术从健康供体全血中分离中性粒细胞。然后用佛波酯12-肉豆蔻酸酯13-乙酸酯(PMA)刺激分离出的中性粒细胞以诱导NETosis。然后丢弃活化的中性粒细胞,获得无细胞NET储备液。接着我们展示了分离出的NETs如何用于与A549人肺癌细胞的黏附试验。将NET储备液用于包被96孔细胞培养板的孔过夜,在确保孔底部形成足够的NET单层后,加入CFSE标记的A549细胞。使用尼康TE300荧光显微镜对贴壁细胞进行定量。在一些孔中,在计数前10分钟加入1000U脱氧核糖核酸酶1以降解NETs。