Aspergillus fumigatus Increased PAR-2 Expression and Elevated Proinflammatory Cytokines Expression Through the Pathway of PAR-2/ERK1/2 in Cornea

被引:56
|
作者
Niu, Yawen [1 ]
Zhao, Guiqiu [1 ]
Li, Cui [1 ]
Lin, Jing [1 ]
Jiang, Nan [1 ]
Che, Chengye [1 ]
Zhang, Jie [1 ]
Xu, Qiang [1 ]
机构
[1] Qingdao Univ, Affiliated Hosp, Dept Ophthalmol, 16 Jiangsu Rd, Qingdao 266003, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
PAR-2; Aspergillus famigatus; keratitis; mice; PROTEASE-ACTIVATED RECEPTOR-2; INNATE IMMUNE-RESPONSE; EPITHELIAL-CELLS; COCKROACH ALLERGEN; INFLAMMATION; FIBROBLASTS; NEUTROPHILS; MODULATE; RELEASE; PAIN;
D O I
10.1167/iovs.17-21887
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE: To determine the role of protease-activated receptor-2 (PAR-2) in cornea infected by Aspergillus fumigatus. METHODS: PAR-2 was tested in normal and infected corneas of C57BL/6 mice. Mice corneas were infected with A. fumigatus with or without pretreatment of PAR-2 antagonist (FSLLRY-NH2). Polymorphonuclear neutrophilic leukocytes (PMNs) were stimulated with 75% ethanol-killed A. fumigatus with or without pretreatment of FSLLRY-NH2. Disease severity was documented by clinical score and photographs with a slit lamp. PCR, Western blot, and ELISA tested expression of PAR-2, IL-1 beta, TNF-alpha, IFN-gamma, MIP-2, and p-ERK1/2. PMN infiltration was assessed by myeloperoxidase assay and immunofluorescent staining. RESULTS: PAR-2 expression was significantly elevated by A. fumigatus, whereas the upregulation was significantly inhibited by FSLLRY-NH2 in mice corneas. FSLLRY-NH2 decreased disease response, PMN infiltration, and proinflammatory cytokine expression compared with infected control. In PMNs, PAR-2 expression was also significantly increased by A. fumigatus, which was significantly inhibited by FSLLRY-NH2. FSLLRY-NH2 significantly inhibited proinflammatory cytokine protein expression, as compared with that in infected control cells, which may be modified by p-ERK1/2. CONCLUSIONS: These data provide evidence that A. fumigatus increased PAR-2 expression and elevated disease, PMN infiltration, and proinflammatory cytokine expression through PAR-2, which may be modified by p-ERK1/2.
引用
收藏
页码:166 / 175
页数:10
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