Vladar Eszter K, Lee Yin Loon, Stearns Tim, Axelrod Jeffrey D
Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Department of Biology, Stanford University, Stanford, CA, USA.
Methods Cell Biol. 2015;127:37-54. doi: 10.1016/bs.mcb.2015.01.016. Epub 2015 Mar 7.
The concerted movement of cilia propels inhaled contaminants out of the lungs, safeguarding the respiratory system from toxins, pathogens, pollutants, and allergens. Motile cilia on the multiciliated cells (MCCs) of the airway epithelium are physically oriented along the tissue axis for directional motility, which depends on the planar cell polarity (PCP) signaling pathway. The MCCs of the mouse respiratory epithelium have emerged as an important model for the study of motile ciliogenesis and the PCP signaling mechanism. Unlike other motile ciliated or planar polarized tissues, airway epithelial cells are relatively easily accessible and primary cultures faithfully model many of the essential features of the in vivo tissue. There is growing interest in understanding how cells acquire and polarize motile cilia due to the impact of mucociliary clearance on respiratory health. Here, we present methods for observing and quantifying the planar polarized orientation of motile cilia both in vivo and in primary culture airway epithelial cells. We describe how to acquire and evaluate electron and light microscopy images of ciliary ultrastructural features that reveal planar polarized orientation. Furthermore, we describe the immunofluorescence localization of PCP pathway components as a simple readout for airway epithelial planar polarization and ciliary orientation. These methods can be adapted to observe ciliary orientation in other multi- and monociliated cells and to detect PCP pathway activity in any tissue or cell type.
纤毛的协同运动将吸入的污染物排出肺部,保护呼吸系统免受毒素、病原体、污染物和过敏原的侵害。气道上皮多纤毛细胞(MCCs)上的运动性纤毛沿组织轴进行物理定向以实现定向运动,这依赖于平面细胞极性(PCP)信号通路。小鼠呼吸道上皮的MCCs已成为研究运动性纤毛发生和PCP信号机制的重要模型。与其他运动性纤毛或平面极化组织不同,气道上皮细胞相对容易获取,原代培养能忠实地模拟体内组织的许多基本特征。由于黏液纤毛清除对呼吸健康的影响,人们对了解细胞如何获得并极化运动性纤毛的兴趣日益浓厚。在此,我们介绍在体内和原代培养气道上皮细胞中观察和量化运动性纤毛平面极化方向的方法。我们描述了如何获取和评估揭示平面极化方向的纤毛超微结构特征的电子显微镜和光学显微镜图像。此外,我们描述了PCP信号通路成分的免疫荧光定位,作为气道上皮平面极化和纤毛方向的简单读数。这些方法可用于观察其他多纤毛和单纤毛细胞中的纤毛方向,并检测任何组织或细胞类型中的PCP信号通路活性。