Department of Otolaryngology, University of Alabama at Birmingham, Birmingham, AL.
Gregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, AL.
Int Forum Allergy Rhinol. 2017 Sep;7(9):920-925. doi: 10.1002/alr.21975. Epub 2017 Jun 28.
Dehydration of airway surface liquid (ASL) disrupts normal mucociliary clearance (MCC) in sinonasal epithelium, which may lead to chronic rhinosinusitis (CRS). Abnormal chloride (Cl ) transport is one such mechanism that contributes to this disorder and can be acquired secondary to environmental perturbations, such as hypoxia at the tissue surface. The objective of this study was to assess the technological feasibility of the novel micro-optical coherence tomography (μOCT) imaging technique for investigating acquired MCC defects in cultured human sinonasal epithelial (HSNE) cells.
Primary HSNE cell cultures were subjected to a 1% oxygen environment for 12 hours to induce acquired cystic fibrosis transmembrane conductance regulator (CFTR) dysfunction. Ion transport characteristics were assessed with pharmacologic manipulation in Ussing chambers. ASL, periciliary fluid (PCL), and ciliary beat frequency (CBF) were evaluated using μOCT.
Amiloride-sensitive transport (ΔI ) was greater in cultures exposed to hypoxia (hypoxia: -13.2 ± 0.6 μA/cm ; control: -6.5 ± 0.1 μA/cm ; p < 0.01), whereas CFTR-mediated anion transport was significantly diminished (hypoxia: 28.6 ± 0.3 μA/cm ; control: 36.2 ± 1.6 μA/cm ; p < 0.01), consistent with acquired CFTR dysfunction and sodium hyperabsorption. Hypoxia diminished all markers of airway surface function microanatomy as observed with μOCT, including ASL (hypoxia: 5.0 ± 0.4 μm; control: 9.0 ± 0.9 μm; p < 0.01) and PCL depth (hypoxia: 2.5 ± 0.1 μm; control: 4.8 ± 0.3 μm; p < 0.01), and CBF (hypoxia: 8.7 ± 0.3 Hz; control: 10.2 ± 0.3 Hz; p < 0.01).
Hypoxia-induced defects in epithelial anion transport in HSNE led to predictable effects on markers of MCC measured with novel μOCT imaging. This imaging method represents a technological leap forward and is feasible for assessing acquired defects impacting the airway surface.
气道表面液体 (ASL) 的脱水会破坏鼻黏膜上皮的正常黏液纤毛清除 (MCC),这可能导致慢性鼻-鼻窦炎 (CRS)。氯离子 (Cl-) 转运异常是导致这种疾病的一种机制,这种异常可能继发于组织表面缺氧等环境改变。本研究的目的是评估新型微光学相干断层扫描 (μOCT) 成像技术在研究培养的人鼻黏膜上皮 (HSNE) 细胞中获得性 MCC 缺陷的技术可行性。
将原代 HSNE 细胞培养物置于 1%氧气环境中 12 小时,以诱导获得性囊性纤维化跨膜电导调节因子 (CFTR) 功能障碍。在 Ussing 室中用药理学方法评估离子转运特性。使用 μOCT 评估 ASL、纤毛周围液 (PCL) 和纤毛摆动频率 (CBF)。
暴露于低氧环境的培养物中的阿米洛利敏感转运 (ΔI) 更高 (低氧:-13.2 ± 0.6 μA/cm;对照:-6.5 ± 0.1 μA/cm;p < 0.01),而 CFTR 介导的阴离子转运显著减少 (低氧:28.6 ± 0.3 μA/cm;对照:36.2 ± 1.6 μA/cm;p < 0.01),与获得性 CFTR 功能障碍和钠吸收过多一致。低氧通过 μOCT 观察到的所有气道表面功能微解剖学标志物都减少,包括 ASL (低氧:5.0 ± 0.4 μm;对照:9.0 ± 0.9 μm;p < 0.01)和 PCL 深度 (低氧:2.5 ± 0.1 μm;对照:4.8 ± 0.3 μm;p < 0.01),以及 CBF (低氧:8.7 ± 0.3 Hz;对照:10.2 ± 0.3 Hz;p < 0.01)。
HSNE 上皮阴离子转运的低氧诱导缺陷导致用新型 μOCT 成像测量的 MCC 标志物出现可预测的变化。这种成像方法是技术上的飞跃,可用于评估影响气道表面的获得性缺陷。