Department of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Chariteí - Universitaätsmedizin Berlin, Berlin, Germany.
German Center for Lung Research (DZL), Associated Partner Site, Berlin, Germany.
Front Immunol. 2022 Feb 28;13:822437. doi: 10.3389/fimmu.2022.822437. eCollection 2022.
The nasal epithelium represents the first line of defense against inhaled pathogens, allergens, and irritants and plays a key role in the pathogenesis of a spectrum of acute and chronic airways diseases. Despite age-dependent clinical phenotypes triggered by these noxious stimuli, little is known about how aging affects the structure and function of the airway epithelium that is crucial for lung homeostasis and host defense. The aim of this study was therefore to determine age-related differences in structural and functional properties of primary nasal epithelial cultures from healthy children and non-smoking elderly people. To achieve this goal, highly differentiated nasal epithelial cultures were established from nasal brushes at air-liquid interface and used to study epithelial cell type composition, mucin (MUC5AC and MUC5B) expression, and ion transport properties. Furthermore, we determined age-dependent molecular signatures using global proteomic analysis. We found lower numeric densities of ciliated cells and higher levels of MUC5AC expression in cultures from children vs. elderly people. Bioelectric studies showed no differences in basal ion transport properties, ENaC-mediated sodium absorption, or CFTR-mediated chloride transport, but detected decreased calcium-activated TMEM16A-mediated chloride secretory responses in cultures from children vs. elderly people. Proteome analysis identified distinct age-dependent molecular signatures associated with ciliation and mucin biosynthesis, as well as other pathways implicated in aging. Our data identified intrinsic, age-related differences in structure and function of the nasal epithelium and provide a basis for further studies on the role of these findings in age-dependent airways disease phenotypes observed with a spectrum of respiratory infections and other noxious stimuli.
鼻上皮是抵御吸入性病原体、过敏原和刺激物的第一道防线,在一系列急、慢性气道疾病的发病机制中起着关键作用。尽管这些有害刺激物会引发与年龄相关的临床表型,但人们对衰老如何影响气道上皮的结构和功能知之甚少,而气道上皮对肺稳态和宿主防御至关重要。因此,本研究旨在确定健康儿童和不吸烟老年人的鼻上皮原代培养物的结构和功能特性是否存在年龄相关性差异。为了实现这一目标,我们在气液界面下从鼻刷中建立了高度分化的鼻上皮培养物,并用于研究上皮细胞类型组成、粘蛋白(MUC5AC 和 MUC5B)表达和离子转运特性。此外,我们还使用全蛋白质组分析确定了年龄依赖性的分子特征。我们发现,与老年人相比,儿童的纤毛细胞数量密度较低,MUC5AC 表达水平较高。生物电化学研究表明,基础离子转运特性、ENaC 介导的钠吸收或 CFTR 介导的氯转运无差异,但检测到儿童的培养物中钙激活 TMEM16A 介导的氯分泌反应降低。蛋白质组分析确定了与纤毛形成和粘蛋白生物合成以及其他与衰老相关的途径相关的独特的年龄依赖性分子特征。我们的数据确定了鼻上皮结构和功能的内在、年龄相关性差异,并为进一步研究这些发现与一系列呼吸道感染和其他有害刺激物引起的与年龄相关的气道疾病表型的关系提供了基础。