Marsico Lung Institute/Cystic Fibrosis Center, School of Medicine, University of North Carolina, Chapel Hill, NC, United States.
Marsico Lung Institute/Cystic Fibrosis Center, School of Medicine, University of North Carolina, Chapel Hill, NC, United States.
Biochem Pharmacol. 2021 May;187:114387. doi: 10.1016/j.bcp.2020.114387. Epub 2021 Jan 5.
Airway epithelial purinergic receptors control key components of the mucociliary clearance (MCC), the dominant component of pulmonary host defense. In healthy airways, the periciliary liquid (PCL) is optimally hydrated, thus acting as an efficient lubricant layer over which the mucus layer moves by ciliary force. When the hydration of the airway surface decreases, the mucus becomes hyperconcentrated, the PCL collapses, and the "thickened" mucus layer adheres to cell surfaces, causing plaque/plug formation. Mucus accumulation is a major contributing factor to the progression of chronic obstructive lung diseases such as cystic fibrosis (CF) and chronic bronchitis (CB). Mucus hydration is regulated by finely tuned mechanisms of luminal Cl secretion and Na absorption with concomitant osmotically driven water flow. These activities are regulated by airway surface liquid (ASL) concentrations of adenosine and ATP, acting on airway epithelial A and P2Y receptors, respectively. The goal of this article is to provide an overview of our understanding of the role of purinergic receptors in the regulation of airway epithelial ion/fluid transport and the mechanisms of nucleotide release and metabolic activities that contribute to airway surface hydration in healthy and chronically obstructed airways.
气道上皮嘌呤能受体控制着黏液纤毛清除(MCC)的关键成分,MCC 是肺部宿主防御的主要成分。在健康的气道中,纤毛周围液体(PCL)得到最佳水合作用,从而起到有效的润滑剂层的作用,使黏液层在纤毛力的作用下移动。当气道表面的水合作用降低时,黏液变得过度浓缩,PCL 坍塌,“增厚”的黏液层附着在细胞表面,导致斑块/塞形成。黏液积聚是慢性阻塞性肺病(如囊性纤维化(CF)和慢性支气管炎(CB))进展的主要因素之一。黏液水合作用受腔内分泌氯离子和吸收钠离子的精细调节机制以及伴随的渗透驱动水流动调节。这些活动受气道表面液体(ASL)中腺苷和 ATP 的浓度调节,分别作用于气道上皮 A 和 P2Y 受体。本文的目的是概述我们对嘌呤能受体在调节气道上皮离子/液体转运以及核苷酸释放和代谢活性机制中的作用的理解,这些机制有助于健康和慢性阻塞气道的气道表面水合作用。