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中性粒细胞通过增加贝赫切特病中性粒细胞胞外诱捕网的释放而导致血管炎。

Neutrophils contribute to vasculitis by increased release of neutrophil extracellular traps in Behçet's disease.

机构信息

Department of Anatomy, Cell Biology and Physiological Science, American University of Beirut, Beirut, Lebanon.

Division of Rheumatology, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.

出版信息

J Dermatol Sci. 2018 Nov;92(2):143-150. doi: 10.1016/j.jdermsci.2018.08.010. Epub 2018 Aug 31.

Abstract

BACKGROUND AND OBJECTIVES

Behçet's disease (BD) is a multi-system inflammatory disorder that can cause vasculitis. Here we questioned whether Neutrophils in BD cause vasculitis via releasing Neutrophil Extracellular Traps (NETs), a process called NETosis.

METHODS

Circulating neutrophils were isolated from a cohort of Middle Eastern BD patients with an active disease and healthy volunteers. The percentage of NETs release was monitored in neutrophils stimulated or not with BD serum, and treated or not with Colchicine, Dexamethasone, Cl-amidine or N-Acetyl Cysteine (NAC). The mRNA expression levels of PAD4 (a key enzyme in NETosis) was also assessed. The effect of NETs on the proliferation and cell death of endothelial cells was investigated using an in vitro co-culture model. The presence of NETs in skin tissues of BD patients was examined using immunolabeling of NETs associated proteins.

RESULTS

Circulating Neutrophils from BD patients were more prone to release NETs in vitro and expressed higher levels of PAD4 compared to healthy volunteers. Spontaneous NETs formation in BD neutrophils was inhibited by Colchicine and Dexamethasone, two drugs used to treat BD. NETs formation was also inhibited by Cl-amidine, a specific PAD4 inhibitor, and by NAC, a ROS inhibitor. Interestingly, serum from BD patients stimulated circulating neutrophils from healthy volunteers to release more NETs and increased their mRNA PAD4 expression. Moreover, endothelial cells cultured in the presence of NETs from BD patients showed a decrease in proliferation and an increase in apoptosis and cell death. Finally, NETosis was predominantly identified around affected blood vessels in biopsies of vasculitis from BD patients.

CONCLUSION

Our results provide evidence on the implication of NETosis in the pathophysiology of BD especially in inducing vasculitis.

摘要

背景与目的

贝赫切特病(BD)是一种多系统炎症性疾病,可引起血管炎。在这里,我们想知道BD 患者的中性粒细胞是否通过释放中性粒细胞胞外诱捕网(NETs)引起血管炎,这个过程称为 NETosis。

方法

从一群中东活动期 BD 患者和健康志愿者中分离循环中性粒细胞。监测在 BD 血清刺激或不刺激、并用秋水仙碱、地塞米松、Cl-amidine 或 N-乙酰半胱氨酸(NAC)处理或不处理的情况下,中性粒细胞释放 NETs 的百分比。还评估了 PAD4(NETosis 的关键酶)的 mRNA 表达水平。使用体外共培养模型研究 NETs 对内皮细胞增殖和细胞死亡的影响。使用 NETs 相关蛋白的免疫标记检查 BD 患者皮肤组织中是否存在 NETs。

结果

与健康志愿者相比,BD 患者的循环中性粒细胞在体外更倾向于释放 NETs,并且表达更高水平的 PAD4。秋水仙碱和地塞米松这两种用于治疗 BD 的药物抑制 BD 中性粒细胞的自发性 NETs 形成。Cl-amidine,一种特异性 PAD4 抑制剂和 NAC,一种 ROS 抑制剂,也抑制 NETs 的形成。有趣的是,BD 患者的血清刺激健康志愿者的循环中性粒细胞释放更多的 NETs,并增加其 mRNA PAD4 表达。此外,在 BD 患者的 NETs 存在的情况下培养的内皮细胞显示增殖减少,凋亡和细胞死亡增加。最后,在 BD 患者的血管炎活检中,主要在受影响的血管周围发现 NETosis。

结论

我们的研究结果提供了 NETosis 在 BD 病理生理学中的作用的证据,特别是在诱导血管炎方面。

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