Centre for Inflammatory Diseases, Department of Medicine, School of Clinical Sciences, Monash University, Clayton, VIC, Australia. Akshay.D'
Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
Methods Mol Biol. 2022;2523:253-263. doi: 10.1007/978-1-0716-2449-4_16.
Neutrophil extracellular traps (NETs) are networks of chromatin and microbicidal proteins released by neutrophils in response to infection and tissue damage. Although classically viewed as a discrete biochemical and cellular process in neutrophils, the effector pathways integrating diverse upstream activating signals to control the formation of NETs (NETosis) are poorly defined. Cell death is one such common unifying endpoint of neutrophils, with several bona fide non-apoptotic cell death agonists now described to initiate NETosis. Integrating these new genetic findings into our existing knowledge of NETosis will likely reveal varied cellular and biochemical processes controlling NET release and specific anti-microbial and inflammatory effector functions of NETs triggered by specific non-apoptotic cell death. To facilitate investigation of regulated cell death pathways in NETosis, we offer a detailed protocol for neutrophil purification from mouse bone marrow and human blood, analysis of NETs by flow cytometry, and validation by immunogold electron microscopy. Future studies may better define cell death-specific forms of NETosis and their influence on inflammation and autoimmunity.
中性粒细胞细胞外陷阱 (NETs) 是中性粒细胞在感染和组织损伤时释放的染色质和杀菌蛋白网络。尽管 NETosis(NETs 的形成)被经典地视为中性粒细胞中的一个离散生化和细胞过程,但整合各种上游激活信号来控制 NETs 形成的效应途径尚未得到明确界定。细胞死亡是中性粒细胞的一个共同统一终点,现在已经描述了几种真正的非凋亡细胞死亡激动剂来启动 NETosis。将这些新的遗传发现纳入我们现有的 NETosis 知识中,可能会揭示控制 NET 释放的各种细胞和生化过程,以及由特定非凋亡细胞死亡触发的 NETs 的特定抗微生物和炎症效应功能。为了促进对 NETosis 中调节性细胞死亡途径的研究,我们提供了从鼠骨髓和人血液中纯化中性粒细胞、通过流式细胞术分析 NETs 以及通过免疫金电子显微镜验证的详细方案。未来的研究可能会更好地定义细胞死亡特异性 NETosis 及其对炎症和自身免疫的影响。