Asthma: a New Approach to the Bronchial Epithelium

Andrius Januškevičius, Eglė Vasylė, Kęstutis Malakauskas
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Abstract

The bronchial epithelium serves as a critical defense line against environmental insults, acting not merely as a barrier but as a complex, dynamic system enriched with diverse cell types such as ciliated cells, goblet cells, and basal cells. Recent advancements in single-cell ribonucleic acid (RNA) sequencing have further unveiled the complexity of this layer by identifying additional cell types like ionocytes, neuroendocrine cells, tuft cells, deuterosomal cells, club cells and mucus ciliated cells. These cells collectively maintain respiratory health through various mechanisms including the mucociliary escalator, mucus production, airway repair, and immune modulation. Disruptions in the epithelial barrier can lead to respiratory diseases like asthma, highlighting the importance of understanding these intricate cellular relationships for developing targeted therapies. This epithelial complexity is crucial for pulmonary homeostasis and the pathogenesis of asthma, where abnormal epithelial remodeling and dysfunction are central. The identification of a novel mucous ciliated cell state in asthma, co-expressing genes associated with both ciliated and goblet cells, offers new insights into the disease’s pathogenesis and therapeutic targets. The epithelial barrier’s integrity, maintained by tight junctions and adherents’ junctions, is essential for protecting the underlying tissue from environmental threats. However, in asthma, this barrier is compromised, leading to increased allergen permeability, airway hyperresponsiveness, inflammation, and remodeling. Despite advances, the need for novel concepts in asthma pathogenesis remains, particularly to address the limitations of the current T helper 2-dominant paradigm in explaining the connection between airway inflammation and remodeling. Understanding the molecular mechanisms underlying epithelial barrier dysfunction could pave the way for novel asthma treatments focused on enhancing barrier integrity, ultimately improving patient outcomes.
哮喘:支气管上皮的新方法
支气管上皮是抵御环境损伤的重要防线,它不仅是一道屏障,还是一个复杂的动态系统,富含多种细胞类型,如纤毛细胞、鹅口疮细胞和基底细胞。单细胞核糖核酸(RNA)测序技术的最新进展进一步揭示了这一层的复杂性,确定了更多的细胞类型,如离子细胞、神经内分泌细胞、簇细胞、脱核细胞、棒状细胞和粘液纤毛细胞。这些细胞通过各种机制共同维持呼吸系统的健康,包括粘液纤毛扶梯、粘液分泌、气道修复和免疫调节。上皮屏障的破坏可导致哮喘等呼吸道疾病,这就凸显了了解这些错综复杂的细胞关系对于开发靶向疗法的重要性。上皮的这种复杂性对肺稳态和哮喘的发病机制至关重要,而上皮的异常重塑和功能障碍是哮喘的核心问题。在哮喘中发现了一种新的粘膜纤毛细胞状态,它同时表达与纤毛细胞和上皮细胞相关的基因,这为了解该疾病的发病机制和治疗目标提供了新的视角。上皮屏障的完整性由紧密连接和粘附连接维持,对于保护下层组织免受环境威胁至关重要。然而,哮喘患者的上皮屏障受到损害,导致过敏原渗透性增加、气道高反应性、炎症和重塑。尽管取得了进展,但哮喘发病机制仍需要新的概念,特别是要解决目前以 T 辅助细胞 2 为主导的模式在解释气道炎症和重塑之间的联系时存在的局限性。了解上皮屏障功能障碍的分子机制可为以增强屏障完整性为重点的新型哮喘治疗铺平道路,最终改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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