Hyperresponsiveness to Extracellular Acidification-Mediated Contraction in Isolated Bronchial Smooth Muscles of Murine Experimental Asthma

• Published in: Lung 2022-10, Vol.200 (5), p.591-599
• Main Authors: Chiba, Yoshihiko, Yamane, Yamato, Sato, Tsubasa, Suto, Wataru, Hanazaki, Motohiko, Sakai, Hiroyasu
• Format: Article
• Language: English
• Subjects: Acidification; Albumin; Analysis; Animal models; Antigens; Asthma; Contractility; Experimental Asthma; G protein-coupled receptors; G proteins; Inflammation; Medicine; Medicine & Public Health; Membrane proteins; Muscle contraction; Muscles; Ovalbumin; pH effects; Pneumology/Respiratory System; Proteins; Protons; Receptors; Respiratory tract; Respiratory tract diseases
• ISSN: 0341-2040; 1432-1750
• DOI: 10.1007/s00408-022-00558-7

Purpose Extracellular acidification is a major component of tissue inflammation, including airway inflammation. The extracellular proton-sensing mechanisms are inherent in various cells including airway structural cells, although their physiological and pathophysiological roles in bronchial smooth muscles (BSMs) are not fully understood. In the present study, to explore the functional role of extracellular acidification on the BSM contraction, the isolated mouse BSMs were exposed to acidic pH under contractile stimulation. Methods and Results The RT-PCR analyses revealed that the proton-sensing G protein-coupled receptors were expressed both in mouse BSMs and cultured human BSM cells. In the mouse BSMs, change in the extracellular pH from 8.0 to 6.8 caused an augmentation of contraction induced by acetylcholine. Interestingly, the acidic pH-induced BSM hyper-contraction was further augmented in the mice that were sensitized and repeatedly challenged with ovalbumin antigen. In this animal model of asthma, upregulations of G protein-coupled receptor 68 (GPR68) and GPR65, that were believed to be coupled with Gq and Gs proteins respectively, were observed, indicating that the acidic pH could cause hyper-contraction probably via an activation of GPR68. However, psychosine, a putative antagonist for GPR68, failed to block the acidic pH-induced responses. Conclusion These findings suggest that extracellular acidification contributes to the airway hyperresponsiveness, a characteristic feature of bronchial asthma. Further studies are required to identify the receptor(s) responsible for sensing extracellular protons in BSM cells.