Department of Pulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ann Am Thorac Soc. 2018 Nov;15(Suppl 3):S164-S170. doi: 10.1513/AnnalsATS.201806-371AW.
Exocytosis of secreted mucins is the final step in their intracellular processing, resulting in their release into the airway lumen to interact with water and ions to form mucus. Mucins are secreted at a low baseline rate and a high stimulated rate, and both rates are regulated by second messengers acting on components of the exocytic machinery. The principal physiologic function of the low baseline rate is to support steady-state mucociliary clearance of inhaled particles and pathogens that enter the airways during normal breathing. Even in the setting of mucin hyperproduction, baseline secretion generally does not induce mucus occlusion. The principal physiologic function of the high stimulated rate of secretion from both submucosal glands and surface goblet cells in proximal airways appears to be to sweep away larger particles, whereas in distal airways it appears to act in concert with mucin hyperproduction to induce mucus occlusion to trap migrating helminths. Pathophysiologically, stimulated mucin secretion in the setting of mucin hyperproduction from allergic or other types of airway inflammation in the absence of helminth infection causes airflow obstruction and infection. Molecular components of the mucin exocytic machinery are increasingly being identified, and surprisingly, many components are not shared between baseline and stimulated machines. The physiologic significance of the presence of two distinct molecular machines is not yet known, such as whether these interact selectively with secretory granules of different sizes or contents. A full understanding of the mechanism and regulation of airway mucin secretion will provide further insight into pathophysiologic processes and may identify therapeutic strategies to alleviate obstructive airway diseases.
分泌粘蛋白的胞吐作用是其细胞内加工的最后一步,导致它们释放到气道腔中与水和离子相互作用形成粘液。粘蛋白以低基础速率和高刺激速率分泌,这两种速率都受作用于胞吐机制成分的第二信使调节。低基础速率的主要生理功能是支持吸入颗粒和在正常呼吸期间进入气道的病原体的稳态黏液纤毛清除。即使在粘蛋白过度产生的情况下,基础分泌通常也不会导致粘液阻塞。来自粘膜下腺和近端气道表面杯状细胞的高刺激分泌速率的主要生理功能似乎是清除较大的颗粒,而在远端气道,它似乎与粘蛋白过度产生协同作用,导致粘液阻塞以捕获迁移的寄生虫。病理生理学上,在没有寄生虫感染的过敏或其他类型的气道炎症导致粘蛋白过度产生的情况下,刺激粘蛋白分泌会导致气流阻塞和感染。粘蛋白胞吐机制的分子成分越来越多地被识别,令人惊讶的是,许多成分在基础和刺激机器之间并不共享。两个不同的分子机器同时存在的生理意义尚不清楚,例如这些机器是否选择性地与不同大小或内容物的分泌颗粒相互作用。对气道粘蛋白分泌的机制和调节的充分理解将进一步深入了解病理生理过程,并可能确定减轻阻塞性气道疾病的治疗策略。