Uric acid induces NADPH oxidase-independent neutrophil extracellular trap formation

被引:109
作者
Arai, Yasuyuki [1 ]
Nishinaka, Yoko [2 ,3 ]
Arai, Toshiyuki [1 ,4 ]
Morita, Makiko [2 ]
Mizugishi, Kiyomi [1 ]
Adachi, Souichi [2 ]
Takaori-Kondo, Akifumi [1 ]
Watanabe, Tomohiro [5 ]
Yamashita, Kouhei [1 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Hematol & Oncol, Kyoto 6068507, Japan
[2] Kyoto Univ, Grad Sch Med, Kyoto 6068507, Japan
[3] Kyoto Univ, Ctr iPS Cell Res & Applicat, Dept Clin Applicat, Kyoto 6068507, Japan
[4] Kyoto City Hosp, Dept Anesthesia, Kyoto 6048845, Japan
[5] Kyoto Univ, Grad Sch Med, Ctr Innovat Immunoregulat Technol & Therapeut, Kyoto 6068507, Japan
基金
日本学术振兴会;
关键词
Uric acid; Neutrophil extracellular trap formation; NADPH oxidase; Chronic granulomatous disease; NE-kappa B; Reactive oxygen species; MYELOPEROXIDASE; MECHANISM; IMMUNITY; DEATH;
D O I
10.1016/j.bbrc.2013.12.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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-kappa B 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. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:556 / 561
页数:6
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