Chiba Yoshihiko, Kusakabe Takashi, Kimura Shioko
Laboratory of Metabolism, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Am J Physiol Lung Cell Mol Physiol. 2004 Dec;287(6):L1193-8. doi: 10.1152/ajplung.00263.2004.
Uteroglobin-related protein 1 (UGRP1) is a secretory protein, highly expressed in epithelial cells of airways. Although an involvement of UGRP1 in the pathogenesis of asthma has been suggested, its function in airways remains unclear. In the present study, a relationship between airway inflammation, UGRP1 expression, and interleukin-9 (IL-9), an asthma candidate gene, was evaluated by using a murine model of allergic bronchial asthma. A severe airway inflammation accompanied by airway eosinophilia and elevation of IL-9 in bronchoalveolar lavage (BAL) fluids was observed after ovalbumin (OVA) challenge to OVA-sensitized mice. In this animal model of airway inflammation, lung Ugrp1 mRNA expression was greatly decreased compared with control mice. A significant inverse correlation between lung Ugrp1 mRNA levels and IL-9 levels in BAL fluid was demonstrated by regression analysis (r = 0.616, P = 0.023). Immunohistochemical analysis revealed a distinct localization of UGRP1 in airway epithelial cells of control mice, whereas UGRP1 staining was patchy and faint in inflamed airways. Intranasal administration of IL-9 to naive mice decreased the level of Ugrp1 expression in lungs. These findings suggest that UGRP1 is downregulated in inflamed airways, such as allergic asthmatics, and IL-9 might be an important mediator for modulating UGRP1 expression.
子宫珠蛋白相关蛋白1(UGRP1)是一种分泌蛋白,在气道上皮细胞中高度表达。尽管已有研究提示UGRP1参与哮喘的发病机制,但其在气道中的功能仍不清楚。在本研究中,我们利用过敏性支气管哮喘小鼠模型,评估了气道炎症、UGRP1表达与哮喘候选基因白细胞介素-9(IL-9)之间的关系。对卵清蛋白(OVA)致敏小鼠进行OVA激发后,观察到严重的气道炎症,伴有气道嗜酸性粒细胞增多以及支气管肺泡灌洗(BAL)液中IL-9水平升高。在这个气道炎症动物模型中,与对照小鼠相比,肺组织Ugrp1 mRNA表达显著降低。回归分析显示,BAL液中肺Ugrp1 mRNA水平与IL-9水平呈显著负相关(r = 0.616,P = 0.023)。免疫组织化学分析显示,对照小鼠气道上皮细胞中UGRP1定位明显,而在炎症气道中UGRP1染色呈斑片状且较弱。对未致敏小鼠鼻内给予IL-9可降低肺组织中Ugrp1的表达水平。这些发现提示,在过敏性哮喘等炎症气道中UGRP1表达下调,且IL-9可能是调节UGRP1表达的重要介质。