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尿酸诱导 NADPH 氧化酶非依赖性中性粒细胞胞外诱捕网形成。

Uric acid induces NADPH oxidase-independent neutrophil extracellular trap formation.

机构信息

Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Human Health Science, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan; Department of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto 606-8507, Japan.

出版信息

Biochem Biophys Res Commun. 2014 Jan 10;443(2):556-61. doi: 10.1016/j.bbrc.2013.12.007. Epub 2013 Dec 8.

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.

摘要

中性粒细胞胞外诱捕网(NETs)是由带有抗菌肽的细胞外 DNA 纤维组成,可以捕获和杀死微生物。NETs 在先天宿主防御以及自身免疫和炎症性疾病中发挥着关键作用。虽然 NET 形成的确切机制尚不清楚,但已知 NADPH 氧化酶(Nox)激活产生的活性氧(ROS)是一个重要的需求。在这项研究中,我们研究了尿酸(UA)对 NET 形成的影响。UA 是一种众所周知的 ROS 清除剂,被发现能够以剂量依赖的方式抑制 Nox 依赖性 ROS 释放。低浓度的 UA 可显著抑制 Nox 依赖性 NET 形成。然而,出乎意料的是,高浓度的 UA 反而诱导了 NET 形成,而不是抑制。UA 可通过 Nox 独立途径直接诱导 NET 形成,这是通过使用 ROS 抑制剂处理的对照中性粒细胞或患有先天性 ROS 产生缺陷的慢性肉芽肿病患者的中性粒细胞进行的实验所揭示的。此外,我们发现 UA 诱导的 NET 形成部分由 NF-κB 激活介导。我们的研究首次证明了 UA 在 NET 形成中的新功能,这可能为高尿酸血症患者的管理提供新的思路。

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