Boucher Dave
Institut de Biochimie, Université de Lausanne, Epalinges, Switzerland.
Bio Protoc. 2019 Sep 5;9(17):e3357. doi: 10.21769/BioProtoc.3357.
Neutrophils are critical immune cells that protect our body against invading pathogens. They generate antibacterial DNA structures called neutrophil extracellular traps (NET). Recently we identified a new mechanism that enables NET formation. We observed that following recognition of lipopolysaccharides, inflammatory caspases cleave Gasdermin D and enable NET generation ( Chen , 2018 ). This protocol describes how we purify neutrophil nuclei to visualize NET formation by live microscopy. After neutrophil purification from murine bone marrow, neutrophils are lysed in a hypotonic buffer using a nitrogen cavitation device to prevent lysis of neutrophil granules and subsequent contamination by granules proteases. Lysed neutrophils are then centrifuged, and nuclei are counted. The protocol described here is straightforward and enables the study of early changes happening in the nuclei of neutrophils undergoing NETosis with limited contamination by granule proteases.
中性粒细胞是关键的免疫细胞,可保护我们的身体免受入侵病原体的侵害。它们会产生一种名为中性粒细胞胞外陷阱(NET)的抗菌DNA结构。最近,我们发现了一种促使NET形成的新机制。我们观察到,在识别脂多糖后,炎性半胱天冬酶会切割Gasdermin D并促使NET生成(Chen,2018年)。本方案描述了我们如何纯化中性粒细胞细胞核,以便通过活细胞显微镜观察NET的形成。从小鼠骨髓中纯化中性粒细胞后,使用氮气空化装置在低渗缓冲液中裂解中性粒细胞,以防止中性粒细胞颗粒溶解以及随后被颗粒蛋白酶污染。然后将裂解后的中性粒细胞离心,并对细胞核进行计数。这里描述的方案简单明了,能够在颗粒蛋白酶污染有限的情况下,研究发生NETosis的中性粒细胞细胞核中的早期变化。