University of British Columbia James Hogg Research Centre--Heart and Lung Institute, St. Paul's Hospital, Vancouver, British Columbia, Canada.
Am J Respir Cell Mol Biol. 2011 Apr;44(4):431-8. doi: 10.1165/rcmb.2010-0146TR. Epub 2010 Aug 19.
Clinical reports of areas of damaged airway epithelium associated with shed epithelial cells in bronchoalveolar lavage fluid, aberrant epithelial repair processes, and altered cytokine and growth factor release have highlighted some fundamental differences between the airway epithelium in individuals with and without asthma. However, the consequences of these epithelial changes are not clearly defined, and may be difficult to assess in the clinic. In this Review, we answer the two questions. (1) What in vivo models and methods have been used to inform us about airway epithelium damage, repair, and immune responses? Our response focuses on genetic influences as well as allergen exposure, environmental/chemical, and mechanical models. (2) How can we improve on existing mouse models to understand changes in airway epithelium biology in asthma? In answering the second question, we include exciting recent studies that have combined multiple exposure methods and/or epithelium-centric outcome measurements. By addressing these two questions, we propose that future interrogation of epithelial responses of both existing and nascent mouse models may provide greater understanding of the mechanisms underlying airway inflammation and remodeling in asthma with hope of generating novel therapeutic targets.
临床报告显示,与哮喘患者和非哮喘患者的气道上皮有关的损伤区域,脱落的上皮细胞在支气管肺泡灌洗液中,异常的上皮修复过程,以及细胞因子和生长因子释放的改变,突出了两者之间的一些基本差异。然而,这些上皮变化的后果尚不清楚,在临床上可能难以评估。在这篇综述中,我们回答了两个问题。(1) 哪些体内模型和方法被用来告知我们关于气道上皮损伤、修复和免疫反应的信息?我们的回答集中在遗传影响以及过敏原暴露、环境/化学和机械模型上。(2) 我们如何改进现有的小鼠模型来了解哮喘中气道上皮生物学的变化?在回答第二个问题时,我们包括了一些令人兴奋的最近的研究,这些研究结合了多种暴露方法和/或上皮中心的结果测量。通过解决这两个问题,我们提出,未来对现有和新生小鼠模型的上皮反应的研究,可能会更好地了解哮喘中气道炎症和重塑的机制,并有望产生新的治疗靶点。