Induction of IL-13 production and upregulation of gene expression of protease activated receptors in P815 cells by IL-6

被引:26
作者
Zhang, Huiyun [2 ]
Lin, Liyan [3 ]
Yang, Haiwei [1 ]
Zhang, Zhongfang [3 ]
Yang, Xiaoyu [3 ]
Zhang, Lianxia [3 ]
He, Shaoheng [1 ,3 ]
机构
[1] Nanjing Med Univ, Clin Res Ctr, Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
[2] Hainan Med Coll, Dept Pathophysiol, Haikou 571101, Hainan, Peoples R China
[3] Shantou Univ, Coll Med, Key Immunopharmacol Lab Guangdong Prov, Allergy & Inflammat Res Inst, Shantou 515041, Peoples R China
基金
中国国家自然科学基金;
关键词
IL-6; IL-13; Mast cell; Protease activated receptor; Tryptase; HUMAN MAST-CELLS; HUMAN ENDOTHELIAL-CELLS; MESSENGER-RNA; INFLAMMATORY MEDIATORS; AIRWAY INFLAMMATION; CYTOKINE EXPRESSION; HISTAMINE-RELEASE; EPITHELIAL-CELLS; P2X(7) RECEPTOR; T-CELLS;
D O I
10.1016/j.cyto.2010.02.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Interleukin (IL)-6 is a multifunctional cytokine which has been showed to induce up-regulated expression of Fe epsilon RI receptor and histamine production in mast cells. However, little is known of its effects on Th2 cytokine secretion and protease activated receptor (PAR) expression in mast cells. In the present study, we examined potential influence of IL-6 on IL-13, IL-4 and IL-10 release from P815 cells and PAR expression on P815 cells by using flow cytometry analysis, quantitative real-time PCR, ELISA and cellular activation of signaling ELISA (CASE) techniques. The results showed that IL-6 induced up to 1.8-fold increase in IL-13, but not IL-4 or IL-10 release from P815 cells, and FSLLRY-NH2 did not affect IL-6 induced IL-13 release. Tryptase elicited 2.0-fold increase in IL-13 release from P815 cells, which can be inhibited by IL-6. IL-6 elicited the up-regulated expression of PAR-1, PAR-2, PAR-3 and PAR-4 mRNAs, but had little effects on expression of PAR proteins. U0126, PD98059 and LY204002 abolished IL-6 induced IL-13 release when they were preincubated with P815 cells, indicating ERK and Akt cell signaling pathways may be involved in the event. In conclusion, IL-6 can stimulate IL-13 release from mast cells through an ERK and Akt cell signaling pathway dependent, but PAR independent mechanism. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:138 / 145
页数:8
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