Liu Jianbo, Zhang Zhenxiang, Xu Yongjian, Xing Lihua, Zhang Huilan
Research Laboratory of Respiratory Diseases, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
J Huazhong Univ Sci Technolog Med Sci. 2004;24(6):575-7. doi: 10.1007/BF02911359.
To study the effects of glucocorticoid on the IL-13-induced Muc5ac expression in airways of mice, and investigate its role in mucus secretion of airways, 24 pathogen-free BALB/c mice were randomly divided into 3 groups. IL-13 group received an nasal instillation of 100 microg of recombinant murine IL-13 solution on days 1, 3 and 5. In dexamethasone group, dexamethasone (0.5 mg/kg) was administered intraperitoneally 24 h before and 1 h before the first instillation of IL-13 and on 4 consecutive days (day 0 to day 5, 6 consecutive days in total), while control group was not treated with IL-13 or dexamethasone. Bronchoalveolar lavage fluid (BALF) was collected and eosinophils were counted, and expression of Muc5ac mRNA and protein in lungs were detected by reverse transcription-polymerase chain reaction (RT-PCR) technology and immunohistochemical assay respectively. Our results showed that the number of mice, with positve Muc5ac protein expression, expression of Muc5ac mRNA and eosinophils in BALF after IL-13 treatment were all significantly higher than that of control group (all P<0.01). Despite eosinophils reduced (P<0.01), the number of mice with positive Muc5ac protein expression, expression of Muc5ac mRNA afterdexamethasone treatment didn't decreas significantly as compared with that of IL-13 group. It is concluded that IL-13 can up-regulate the expression of Muc5ac mRNA and protein, which may play a pivotal role in the mucus overproduction of airways. Dexamethasone can suppress IL-13-induced eosinophilic infiltration in lung but can't inhibit the mucus overproduction.
为研究糖皮质激素对白细胞介素-13(IL-13)诱导的小鼠气道Muc5ac表达的影响,并探讨其在气道黏液分泌中的作用,将24只无特定病原体的BALB/c小鼠随机分为3组。IL-13组在第1、3和5天经鼻滴注100μg重组小鼠IL-13溶液。地塞米松组在首次滴注IL-13前24小时和前1小时腹腔注射地塞米松(0.5mg/kg),并连续4天(第0天至第5天,共6天)给药,而对照组不给予IL-13或地塞米松。收集支气管肺泡灌洗液(BALF)并计数嗜酸性粒细胞,分别采用逆转录-聚合酶链反应(RT-PCR)技术和免疫组织化学方法检测肺组织中Muc5ac mRNA和蛋白的表达。结果显示,IL-13处理后,Muc5ac蛋白表达阳性的小鼠数量、Muc5ac mRNA表达及BALF中嗜酸性粒细胞数量均显著高于对照组(均P<0.01)。地塞米松处理后,尽管嗜酸性粒细胞减少(P<0.01),但Muc5ac蛋白表达阳性的小鼠数量、Muc5ac mRNA表达与IL-13组相比无显著下降。结论:IL-13可上调Muc5ac mRNA和蛋白的表达,这可能在气道黏液过度分泌中起关键作用。地塞米松可抑制IL-13诱导的肺部嗜酸性粒细胞浸润,但不能抑制黏液过度分泌。