Tanshinone IIA ameliorates chronic arthritis in mice by modulating neutrophil activities

被引:48
作者
Zhang, S. [1 ]
Huang, G. [1 ]
Yuan, K. [1 ]
Zhu, Q. [1 ]
Sheng, H. [1 ]
Yu, R. [1 ]
Luo, G. [1 ]
Xu, A. [1 ,2 ]
机构
[1] Beijing Univ Chinese Med, Sch Life Sci, 11 Beisanhuandong Rd, Beijing 100029, Peoples R China
[2] Sun Yat Sen Zhongshan Univ, Sch Life Sci, Dept Biochem, State Key Lab Biocontrol, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
arthritis; inflammation; neutrophil; tanshinone IIA; RHEUMATOID-ARTHRITIS; VASCULAR ENDOTHELIUM; INFLAMMATION; APOPTOSIS; CELLS; RECRUITMENT; ACTIVATION; REGULATORS; CYTOKINES; EFFECTORS;
D O I
10.1111/cei.12993
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Rheumatoid arthritis (RA) is a chronic immune inflammatory disease mediated by the influx of immune cells into the synovial joint space. As Tanshinone IIA (TIIA) has potent anti-oxidant and anti-inflammatory activities, we used the adjuvant-induced arthritis (AA) murine model of RA to investigate the impact of TIIA on RA and immune cell activation. The anti-arthritic activity of TIIA was investigated in an adjuvant-induced arthritis model of RA in mice. Myeloperoxidase and neutrophil elastase expression levels were assessed in ankle joints by immunohistochemistry analysis. Immune cell infiltration was evaluated in air pouch experiments. Proinflammatory cytokines expression levels were determined by quantitative real-time polymerase chain reaction (PCR) and enzyme-linked immunosorbent assays. Neutrophil extracellular traps (NETs) were assessed by immunostaining and confocal microscopy. Treatment with TIIA alleviated cartilage erosion and neutrophil infiltration in the ankle joints of AA mice and reduced proinflammatory cytokine expression levels in sera. TIIA suppressed interleukin-6 and tumour necrosis factor- expression and release in neutrophils and promoted neutrophil apoptosis. TIIA also inhibited the NET formation of neutrophils. Our findings demonstrated that TIIA can ameliorate RA effectively by targeting neutrophils, indicating that TIIA may act as a potential therapeutic for RA.
引用
收藏
页码:29 / 39
页数:11
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