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Simplified Human Neutrophil Extracellular Traps (NETs) Isolation and Handling

机译:简化的人类嗜中性粒细胞细胞外陷阱(NETs)的分离和处理

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摘要

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
机译:中性粒细胞胞外陷阱(NETs)最近被确定为中性粒细胞抗菌武器库的一部分。除了它们在抵抗感染中的作用外,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,我们演示了使用容易获得的试剂从人全血中分离无细胞NET的简化方法。然后可以将分离的NET用于免疫荧光染色,印迹或各种功能测定。这样就可以在没有嗜中性粒细胞自身潜在混杂效应的情况下评估其生物学特性。采用密度梯度分离技术从健康供体全血中分离嗜中性粒细胞。然后通过佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)刺激分离的中性粒细胞,以诱导NETosis。然后丢弃活化的嗜中性粒细胞,获得无细胞的NET储备液。然后我们证明了分离的NETs如何用于A549人肺癌细胞的粘附测定。使用NET储备液覆盖96孔细胞培养板O / N的孔,并确保在孔底部形成足够的NET单层后,添加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。在某些孔中,在计数以降解NET之前10分钟添加1000U DNAse1

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