Neutrophil Extracellular Traps (NETs) in health and disease

中性粒细胞胞外陷阱 免疫学 免疫系统 中性粒细胞弹性蛋白酶 组蛋白 染色质 细胞生物学 生物 先天免疫系统 自身免疫 自身免疫性疾病 细胞外 炎症 疾病 吞噬作用 传出细胞增多 瓜氨酸化 核小体 系统性红斑狼疮 传染病(医学专业) 粒细胞 抗菌肽 生物膜 自身抗体 化学 弹性蛋白酶 癌症研究 医学 微生物学 诱饵 抗菌剂 癌症 红斑狼疮 抗体 细胞内 细胞 转化医学
作者
Asif Shahzad,Yueli Ni,Yinfeng Yang,Wenjing Liu,Zhuoran Teng,Honggang Bai,Xiangjie Liu,Yijian Sun,Jiaojiao Xia,Kun Cui,Qiuxin Duan,Zhe Xü,Jinshan Zhang,Zhe Yang,Qiao Zhang
出处
期刊:Molecular biomedicine [Springer Nature]
卷期号:6 (1): 130-130 被引量:36
标识
DOI:10.1186/s43556-025-00337-9
摘要

Neutrophil extracellular traps (NETs) are web-like structures composed of DNA, histones, and antimicrobial proteins that extend the defensive repertoire of neutrophils beyond classical phagocytosis and degranulation. Initially considered solely antimicrobial, NETs are now recognized as dynamic regulators of immunity, inflammation, and tissue remodeling. Their formation is orchestrated by the generation of reactive oxygen species, neutrophil elastase-mediated chromatin remodeling, and peptidyl arginine deiminase 4-driven histone citrullination. At the same time, clearance involves DNase activity and macrophage-mediated phagocytosis. In physiological contexts, NETs immobilize and kill pathogens, restrict biofilm formation, and coordinate immune cell crosstalk, thereby supporting host defense and repair. However, when NET formation or clearance becomes dysregulated, these structures drive a broad spectrum of pathologies. Aberrant NET activity has been implicated in infectious diseases (bacterial, viral, fungal), autoimmune disorders such as systemic lupus erythematosus, ANCA-associated vasculitis, rheumatoid arthritis, Gout, and psoriasis, cardiovascular disorders including atherosclerosis, thrombosis, acute coronary syndrome, Myocardial ischemia/reperfusion injury, hypertension, atrial fibrillation, heart failure, and viral myocarditis, as well as cancer progression, metastasis, and other inflammation-associated disorders such as asthma, Alzheimer's disease, diabetes, and pregnancy-related complications. Advances in imaging, proteomics, and single-cell sequencing have expanded our ability to characterize NETs across contexts, revealing stimulus- and disease-specific heterogeneity. At the translational levels, therapies that inhibit NETs formation, promote their degradation, or regulate their release, including PAD4 and elastase inhibitors, DNase-based approaches, and antibody strategies, are under active investigation. By integrating these advances, this review provides a framework for translating NET biology into clinically relevant applications.
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