Opposing roles of IL-17A and IL-25 in the regulation of TSLP production in human nasal epithelial cells

被引:80
作者
Xu, G. [1 ,2 ]
Zhang, L. [3 ]
Wang, D. Y. [4 ]
Xu, R. [1 ]
Liu, Z. [5 ]
Han, D. M. [3 ]
Wang, X. D. [3 ]
Zuo, K. J. [1 ,2 ]
Li, H. B. [1 ,2 ,3 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Otorhinolaryngol Hosp, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Otorhinolaryngol Inst, Guangzhou 510080, Guangdong, Peoples R China
[3] Capital Med Univ, Beijing Tongren Hosp, Dept Otolaryngol, Beijing, Peoples R China
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Otolaryngol, Singapore 117595, Singapore
[5] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Otolaryngol, Wuhan 430074, Peoples R China
关键词
allergic rhinitis; IL-17; family; nasal epithelial cells; nasal lavage; thymic stromal lymphopoietin; THYMIC STROMAL LYMPHOPOIETIN; ASTHMATIC AIRWAYS; INTERLEUKIN-17; INFLAMMATION; EXPRESSION;
D O I
10.1111/j.1398-9995.2009.02252.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: The importance of IL-17A, IL-17F, and IL-25 in allergic rhinitis (AR), as well as their possible role in regulation on thymic stromal lymphopoietin (TSLP) production in nasal epithelial cells, is not well understood. Objective: To determine the possible regulation of IL-17A, IL-17F, and IL-25 on TSLP production in the initiation of allergic responses. Methods: The levels of IL-17A, IL-17F, IL-25, and TSLP in nasal lavages of patients with AR were measured using an enzyme-linked immunosorbent assay (ELISA) and compared with that in normal controls. Then, primary human nasal epithelial cells (HNECs) were stimulated with dsRNA (0-75 mu g/ml), as well as IL-17A (100 ng/ml), IL-17F (100 ng/ml), and IL-25(100 ng/ml). The mRNA expression of IL-17A, IL-17F, IL-25, TSLP, as well as the chemokines CCL20, IL-8, and eotaxin was analyzed using quantitative real-time PCR, and their protein levels in the supernatants of cultured HNECs were determined by ELISA. Results: Both TSLP and IL-17 cytokines are significantly elevated in patients with AR. dsRNA was found to increase the production of IL-17F, IL-25, TSLP, CCL20, and IL-8 in HNECs. Furthermore, IL-25 significantly enhanced dsRNA-induced TSLP production in primary HNECs and was dominant to the inhibitory effect of IL-17A on TSLP regulation. Conclusions: Our study provides the first evidence that both IL-17F and IL-25 can be induced by dsRNA in HNECs. Despite of the opposing effects of IL-17A and IL-25 on TSLP regulation in HNECs, IL-25 was dominant to IL-17A, providing a plausible explanation for the simultaneous upregulation of IL-17 cytokines and TSLP in patients with AR.
引用
收藏
页码:581 / 589
页数:9
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