You Yingjian, Brody Steven L
Department of Internal Medicine, School of Medicine, Washington University in St. Louis, Saint Louis, MO, USA.
Methods Mol Biol. 2013;945:123-43. doi: 10.1007/978-1-62703-125-7_9.
Airway epithelial cell biology has been greatly advanced by studies of genetically defined and modified mice; however it is often difficult to isolate, manipulate, and assay epithelial cell-specific responses in vivo. In vitro proliferation and differentiation of mouse airway epithelial cells are made possible by a high-fidelity system for primary culture of mouse tracheal epithelial cells described in this chapter. Using this method, epithelial cells purified from mouse tracheas proliferate in growth factor-enriched medium. Subsequent culture in defined medium and the use of the air-liquid interface condition result in the development of well-differentiated epithelia composed of ciliated and non-ciliated cells with characteristics of native airways. Methods are also provided for manipulation of differentiation and analysis of differentiation and gene expression. These approaches allow the assessment of global responses and those of specific cell subpopulations within the airway epithelium.
通过对基因定义和修饰小鼠的研究,气道上皮细胞生物学取得了巨大进展;然而,在体内分离、操纵和检测上皮细胞特异性反应往往很困难。本章所述的小鼠气管上皮细胞原代培养的高保真系统使小鼠气道上皮细胞的体外增殖和分化成为可能。使用这种方法,从小鼠气管中纯化的上皮细胞在富含生长因子的培养基中增殖。随后在特定培养基中培养并使用气液界面条件,会导致由具有天然气道特征的纤毛细胞和非纤毛细胞组成的高度分化上皮的发育。还提供了操纵分化以及分析分化和基因表达的方法。这些方法允许评估气道上皮内的整体反应以及特定细胞亚群的反应。