Department of Surgery/Division of Otolaryngology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
PLoS One. 2013 Nov 25;8(11):e81589. doi: 10.1371/journal.pone.0081589. eCollection 2013.
Chronic rhinosinusitis engenders enormous morbidity in the general population, and is often refractory to medical intervention. Compounds that augment mucociliary clearance in airway epithelia represent a novel treatment strategy for diseases of mucus stasis. A dominant fluid and electrolyte secretory pathway in the nasal airways is governed by the cystic fibrosis transmembrane conductance regulator (CFTR). The objectives of the present study were to test resveratrol, a strong potentiator of CFTR channel open probability, in preparation for a clinical trial of mucociliary activators in human sinus disease.
Primary sinonasal epithelial cells, immortalized bronchoepithelial cells (wild type and F508del CFTR), and HEK293 cells expressing exogenous human CFTR were investigated by Ussing chamber as well as patch clamp technique under non-phosphorylating conditions. Effects on airway surface liquid depth were measured using confocal laser scanning microscopy. Impact on CFTR gene expression was measured by quantitative reverse transcriptase polymerase chain reaction.
Resveratrol is a robust CFTR channel potentiator in numerous mammalian species. The compound also activated temperature corrected F508del CFTR and enhanced CFTR-dependent chloride secretion in human sinus epithelium ex vivo to an extent comparable to the recently approved CFTR potentiator, ivacaftor. Using inside out patches from apical membranes of murine cells, resveratrol stimulated an ~8 picosiemens chloride channel consistent with CFTR. This observation was confirmed in HEK293 cells expressing exogenous CFTR. Treatment of sinonasal epithelium resulted in a significant increase in airway surface liquid depth (in µm: 8.08+/-1.68 vs. 6.11+/-0.47,control,p<0.05). There was no increase CFTR mRNA.
Resveratrol is a potent chloride secretagogue from the mucosal surface of sinonasal epithelium, and hydrates airway surface liquid by increasing CFTR channel open probability. The foundation for a clinical trial utilizing resveratrol as a therapeutic intervention to increase mucociliary transport and airway surface liquid hydration in sinus disease is strongly supported by these findings.
慢性鼻窦炎在普通人群中造成了巨大的发病率,并且经常对医学干预产生抗药性。增强气道上皮纤毛清除率的化合物代表了黏液停滞性疾病的一种新的治疗策略。鼻气道中主要的液体和电解质分泌途径受囊性纤维化跨膜电导调节剂(CFTR)控制。本研究的目的是测试白藜芦醇,一种 CFTR 通道开放概率的强增强剂,为人类鼻窦疾病中粘液纤毛激活剂的临床试验做准备。
通过 Ussing 室和非磷酸化条件下的膜片钳技术,对原代鼻内上皮细胞、永生化的支气管上皮细胞(野生型和 F508del CFTR)和表达外源性人 CFTR 的 HEK293 细胞进行了研究。使用共聚焦激光扫描显微镜测量气道表面液体深度。通过定量逆转录聚合酶链反应测量对 CFTR 基因表达的影响。
白藜芦醇是许多哺乳动物物种中强大的 CFTR 通道增强剂。该化合物还激活了温度校正的 F508del CFTR,并增强了人鼻窦上皮细胞 ex vivo 中 CFTR 依赖性氯离子分泌,程度可与最近批准的 CFTR 增强剂 ivacaftor 相媲美。使用来自鼠细胞顶膜的内面向片,白藜芦醇刺激了一个约 8 皮西门子氯离子通道,与 CFTR 一致。这一观察结果在表达外源性 CFTR 的 HEK293 细胞中得到了证实。对鼻内上皮细胞的处理导致气道表面液体深度显著增加(以 µm 计:8.08+/-1.68 与 6.11+/-0.47,对照,p<0.05)。CFTR mRNA 没有增加。
白藜芦醇是鼻内上皮黏膜表面的一种有效的氯离子分泌剂,通过增加 CFTR 通道开放概率来增加气道表面液体的水分。这些发现强烈支持了利用白藜芦醇作为治疗干预措施,增加鼻窦疾病中粘液纤毛转运和气道表面液体水合作用的临床试验的基础。