Decreased ciliary beat responsiveness to acetylcholine in the nasal polyp epithelium

医学 乙酰胆碱 鼻粘膜 毒蕈碱乙酰胆碱受体 嘌呤能受体 纤毛 免疫组织化学 病理 内科学 受体 内分泌学 解剖 生物 细胞生物学
作者
Ba Hung,Toyoaki Ohbuchi,Mitsuru Yokoyama,Takuro Kitamura,Tetsuro Wakasugi,Jun‐ichi Ohkubo,Hideaki Suzuki
出处
期刊:Clinical Otolaryngology [Wiley]
卷期号:44 (3): 356-365 被引量:13
标识
DOI:10.1111/coa.13312
摘要

Objective We investigated the difference in ciliary beat responsiveness to acetylcholine in ex vivo and the difference in the expressions of associated molecules (M1/M3 muscarinic receptors, pannexin‐1 and P2X7 purinergic receptor) between the nasal polyp and turbinate mucosa. Study design Laboratorial study. Participants Nasal polyp and inferior turbinate were collected from patients with hypertrophic rhinitis and/or nasal polyp during endoscopic sinonasal surgery. Main outcome measures The mucosa was cut into thin strips, and ciliary movement was observed under a phase‐contrast light microscope equipped with a high‐speed digital video camera. The samples were also examined by scanning electron microscopy, fluorescence immunohistochemistry, and quantitative reverse transcription‐polymerase chain reaction. Results Cilia were well preserved in both tissues at the ultrastructural level. The baseline ciliary beat frequency (CBF) was not different between the two tissues. The CBF of the turbinate was significantly increased by stimulation with acetylcholine ( P < 0.001), but that of the polyp was not. The ratio of the acetylcholine‐stimulated CBF to the baseline CBF was significantly lower in the polyp than in the turbinate ( P < 0.001). Immunohistochemical study revealed that immunoreactivities for M3, pannexin‐1 and P2X7 were weaker in the polyp than in the turbinate. The mRNA expressions of M1, M3 and P2X7 were significantly lower and that of pannexin‐1 tended to be lower in the polyp than in the turbinate. Conclusions These results indicate that ciliary beat responsiveness to acetylcholine is decreased in the nasal polyp. This may be explained by the decreased expressions of M3, P2X7 and probably pannexin‐1 in this tissue.
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