The effects of Th2 cytokines on the expression of ADAM33 in allergen-induced chronic airway inflammation

被引:48
作者
Jie, Zhijun [1 ]
Jin, Meiling [1 ]
Cai, Yingyun [1 ]
Bai, Chunxue [1 ]
Shen, Yao [1 ]
Yuan, Zhenghong [2 ]
Hu, Yunwen [2 ]
Holgate, Stephen [3 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Resp Med, Shanghai 200032, Peoples R China
[2] Fudan Univ, Shanghai Med Coll, Key Lab Med Mol Virol, Shanghai 200032, Peoples R China
[3] Univ Southampton, Sch Med, Southampton, Hants, England
基金
英国医学研究理事会;
关键词
ADAM33; Airway inflammation; Airway remodeling; Mice; Fibroblasts; BRONCHIAL HYPERRESPONSIVENESS; ASTHMA; POLYMORPHISMS; ASSOCIATION; GENE; DISINTEGRIN; MOUSE; IDENTIFICATION; POPULATION; PROTEIN;
D O I
10.1016/j.resp.2009.07.019
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
A disintegrin and metalloprotease domain 33 (ADAM33) has been identified as an asthma susceptibility gene, which is associated with small-airway remodeling. However, the role of ADAM33 in the development of allergic airway inflammation is unclear. The present study used an established murine model of allergen-induced chronic airway inflammation, which was sensitized and then challenged by nebulized 2.5% ovalbumin (OVA) for 8 weeks (30 min/day, three times a week). The expression of ADAM33 mRNA detected by real time RT-PCR was significantly enhanced in the lung tissue of mice with OVA challenge. as compared with the group challenged with saline. This OVA-challenged model showed significant Th2-biased airway inflammation as well as airway remodeling with features of sub-epithelial fibrosis and mucus hyper-secretion. Furthermore, in vitro studies showed that IL-4 and IL-13 could significantly upregulate the expression of ADAM33 mRNA in human fibroblasts in a concentration- and time-dependent manner as compared to normal controls. These results support the note that Th2 cytokines can up-regulate the expression of ADAM33 mRNA and ADAM33 may play an important role in the development of airway remodeling in allergen-induced chronic airway inflammation. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:289 / 294
页数:6
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