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CD69 expression on airway eosinophils and airway inflammation in a murine model of asthma

CD69 expression on airway eosinophils and airway inflammation in a murine model of asthma

作     者:WANG Hui-ying SHEN Hua-hao James J Lee Nancy A Lee 

作者机构:Department of Respiratory Medicine Second Affiliated Hospital ofZhejiang University Medical College Institute of RespiratoryDiseases of Zhejiang University Hangzhou 310009 China Department of Biochemistry and Molecular Biology Mayo ClinicScottsdale Scottsdale Arizona 85259 USA 

出 版 物:《Chinese Medical Journal》 (中华医学杂志(英文版))

年 卷 期:2006年第119卷第23期

页      面:1983-1990页

核心收录:

学科分类:1002[医学-临床医学] 100201[医学-内科学(含:心血管病、血液病、呼吸系病、消化系病、内分泌与代谢病、肾病、风湿病、传染病)] 10[医学] 

基  金:This work was partially supported by the National Natural Science Foundation of China (No. 30570807) 

主  题:asthma eosinophils CD69 airway inflammation murine model 

摘      要:Background Asthma is a chronic airway disease with inflammation characterized by physiological changes (airway hyper-responsiveness, AHR) and pathological changes (inflammatory cells infiltration and mucus production). Eosinophils play a key role in the allergic inflammation. But the causative relationship between eosinophils and airway inflammation is hard to prove. One of the reasons is lack of activation marker of murine eosinophils. We investigated the expression of CD69 on murine eosinophils in vitro, the relationship between the expression of CD69 on eosinophils from peripheral blood and bronchoalveolar lavage fluid and on airway inflammation in asthmatic mice. Methods Eosinophils from peripheral blood of IL-5 transgenic mice (NJ.1638) were purified. Mice were divided into five groups: wild type mice sensitized and challenged with saline (WS group), wild type mice sensitized and challenged with ovalbumin (WO group), IL-5^-/- mice sensitized and challenged with saline and transferred with purified eosinophils (ISE group), IL-5^-/- mice sensitized and challenged with OVA and transferred with purified eosinophils (IOE group), IL-5^-/- mice sensitized and challenged with OVA and transferred with purified eosinophils, pretreated with anti CD4 monoclonal antibody (IOE+antiCD4mAb group). IL-5^-/- mice were sensitized with OVA at day 0 and day 14, then challenged with OVA aerosol. On days 24, 25, 26 and 27 purified eosinophils were transferred intratracheally to IL-5^-/- mice. On day 28, blood and BALF were collected and CD69 expression on eosinophils measured by flowcytometry. Results Purified eosinophils did not express CD69. But eosinophils cultured with PMA+MA, IFN- T, IL-5 or GM-CSF expressed CD69 strongly. Eosinophils from blood of WO, WS group did not express CD69 at all. The numbers of eosinophils in BALF of WO group, IOE group, ISE group and IOE+antiCD4mAb group were significantly higher than in mice of WS group which did not have eosinophils at all. CD69

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