中性粒细胞胞外陷阱
NADPH氧化酶
活性氧
高尿酸血症
化学
尿酸
黄嘌呤氧化酶
氮氧化物
氧化酶试验
先天免疫系统
细胞外
生物化学
细胞生物学
炎症
免疫学
生物
受体
酶
有机化学
燃烧
作者
Yasuyuki Arai,Yoko Nishinaka,Toshiyuki Arai,Maki Morita,Kiyomi Mizugishi,Souichi Adachi,Akifumi Takaori‐Kondo,Tomohiro Watanabe,Kouhei Yamashita
标识
DOI:10.1016/j.bbrc.2013.12.007
摘要
Neutrophil extracellular traps (NETs) are composed of extracellular DNA fibers with antimicrobial peptides that capture and kill microbes. NETs play a critical role in innate host defense and in autoimmune and inflammatory diseases. While the mechanism of NET formation remains unclear, reactive oxygen species (ROS) produced via activation of NADPH oxidase (Nox) are known to be an important requirement. In this study, we investigated the effect of uric acid (UA) on NET formation. UA, a well-known ROS scavenger, was found to suppress Nox-dependent ROS release in a dose-dependent manner. Low concentrations of UA significantly inhibited Nox-dependent NET formation. However, high concentrations of UA unexpectedly induced, rather than inhibited, NET formation. NETs were directly induced by UA alone in a Nox-independent manner, as revealed by experiments using control neutrophils treated with ROS inhibitors or neutrophils of patients with chronic granulomatous disease who have a congenital defect in ROS production. Furthermore, we found that UA-induced NET formation was partially mediated by NF-κB activation. Our study is the first to demonstrate the novel function of UA in NET formation and may provide insight into the management of patients with hyperuricemia.
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