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Uric acid induces NADPH oxidase-independent neutrophil extracellular trap formation
Authors:Yasuyuki Arai  Yoko Nishinaka  Toshiyuki Arai  Makiko Morita  Kiyomi Mizugishi  Souichi Adachi  Akifumi Takaori-Kondo  Tomohiro Watanabe  Kouhei Yamashita
Affiliation:1. Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan;2. Human Health Science, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan;3. Department of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto 606-8507, Japan;4. Department of Anesthesia, Kyoto City Hospital, Kyoto 604-8845, Japan;5. Center for Innovation in Immunoregulative Technology and Therapeutics, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan
Abstract: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.
Keywords:CGD, chronic granulomatous disease   DHR, dihydrorhodamine 123   DPI, diphenyleneiodonium   HBSS, Hanks&rsquo   balanced salt solution   MSU, monosodium urate   MVP, trans-1-(2&prime  -methoxyvinyl)pyrene   Nox, NADPH oxidase   NET, neutrophil extracellular trap   PBN, α-phenyl-N-tert-butyl nitrone   PMA, phorbol myristate acetate   ROS, reactive oxygen species   1O2, singlet oxygen   UA, uric acid
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