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自噬由抗中性粒细胞胞浆抗体诱导,并促进中性粒细胞胞外诱捕网的形成。

Autophagy is induced by anti-neutrophil cytoplasmic Abs and promotes neutrophil extracellular traps formation.

作者信息

Sha Li-Li, Wang Huan, Wang Chen, Peng Hong-Ying, Chen Min, Zhao Ming-Hui

机构信息

1 Renal Division, Department of Medicine, Peking University First Hospital; Peking University Institute of Nephrology; Key Laboratory of Renal Disease, Ministry of Health of China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment (Peking University), Ministry of Education, China.

2 Guizhou Medical University, China.

出版信息

Innate Immun. 2016 Nov;22(8):658-665. doi: 10.1177/1753425916668981. Epub 2016 Sep 26.

DOI:10.1177/1753425916668981
PMID:27670946
Abstract

Dysregulated neutrophil extracellular traps (NETs) formation contributes to the pathogenesis of anti-neutrophil cytoplasmic Ab (ANCA)-associated vasculitis (AAV). Increasing evidence indicates that autophagy is involved in the process of NETs formation. In this study, we aimed to investigate whether ANCA could induce autophagy in the process of NETs formation. Autophagy was detected using live cell imaging, microtubule-associated protein light chain 3B (LC3B) accumulation and Western blotting. The results showed that autophagy vacuolization was detected in neutrophils treated with ANCA-positive IgG by live cell imaging. This effect was enhanced by rapamycin, the autophagy inducer, and weakened by 3-methyladenine (3-MA), the autophagy inhibitor. In line with these results, the autophagy marker, LC3B, showed a punctate distribution pattern in the neutrophils stimulated with ANCA-positive IgG. In the presence of rapamycin, LC3B accumulation was further increased; however, this effect was attenuated by 3-MA. Moreover, incubated with ANCA-positive IgG, the NETosis rate significantly increased compared with the unstimulated group. And, the rate significantly increased or decreased in the neutrophils pretreated with rapamycin or 3-MA, respectively, as compared with the cells incubated with ANCA-positive IgG. Overall, this study demonstrates that autophagy is induced by ANCA and promotes ANCA-induced NETs formation.

摘要

中性粒细胞胞外陷阱(NETs)形成失调有助于抗中性粒细胞胞浆抗体(ANCA)相关血管炎(AAV)的发病机制。越来越多的证据表明自噬参与了NETs形成过程。在本研究中,我们旨在探讨ANCA是否能在NETs形成过程中诱导自噬。使用活细胞成像、微管相关蛋白轻链3B(LC3B)积累和蛋白质免疫印迹法检测自噬。结果显示,通过活细胞成像在经ANCA阳性IgG处理的中性粒细胞中检测到自噬空泡化。自噬诱导剂雷帕霉素增强了这种效应,而自噬抑制剂3-甲基腺嘌呤(3-MA)则削弱了这种效应。与这些结果一致,自噬标志物LC3B在经ANCA阳性IgG刺激的中性粒细胞中呈现点状分布模式。在雷帕霉素存在的情况下,LC3B积累进一步增加;然而,3-MA减弱了这种效应。此外,与未刺激组相比,用ANCA阳性IgG孵育后,NETosis率显著增加。并且,与用ANCA阳性IgG孵育的细胞相比,分别用雷帕霉素或3-MA预处理的中性粒细胞中,该比率显著增加或降低。总体而言,本研究表明ANCA诱导自噬并促进ANCA诱导的NETs形成。

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