Cell and Cancer Biology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
PLoS One. 2012;7(8):e43008. doi: 10.1371/journal.pone.0043008. Epub 2012 Aug 16.
Clara cells are non-ciliated, secretory bronchiolar epithelial cells that serve to detoxify harmful inhaled substances. Clara cells also function as stem/progenitor cells for repair in the bronchioles. Clara cell secretory protein (CCSP) is specifically expressed in pulmonary Clara cells and is widely used as a Clara cell marker. In addition CCSP promoter is commonly used to direct gene expression into the lung in transgenic models. The discovery of CCSP immunoreactivity in plasma membranes of airway lining cells prompted us to explore the possibility of enriching Clara cells by flow cytometry. We established a novel and simple method for the isolation of CCSP-expressing cell Clara cells using a combination of mechanical and enzymatic dissociation followed by flow cytometry sorting technology. We showed that ∼25% of dissociated cells from whole lung expressed CCSP. In the resulting preparation, up to 98% of cells expressed CCSP. Notably, we found that several common stem cell markers including CD44, CD133, Sca-1 and Sox2 were expressed in CCSP(+) cells. Moreover, CCSP(+) cells were able to form spheroid colonies in vitro with 0.97‰ efficiency. Parallel studies in vivo confirmed that a small population of CCSP(-)expressing cells in mouse airways also demonstrates stem cell-like properties such as label retention and harboring rare bronchioalveolar stem cells (BASCs) in terminal bronchioles (TBs). We conclude that CCSP(+) cells exhibit a number of stem cell-like features including stem cell marker expression, bronchosphere colony formation and self-renewal ability. Clara cell isolation by flow cytometry sorting is a useful method for investigating the function of primary Clara cells in stem cell research and mouse models.
克拉拉细胞是无纤毛的、分泌性的细支气管上皮细胞,有助于解毒吸入的有害物质。克拉拉细胞还作为细支气管的干细胞/祖细胞发挥作用。克拉拉细胞分泌蛋白 (CCSP) 特异性表达于肺的克拉拉细胞,广泛用作克拉拉细胞的标志物。此外,CCSP 启动子通常用于在转基因模型中将基因表达导向肺部。CCSP 免疫反应性在气道衬里细胞的质膜中被发现,促使我们探索通过流式细胞术富集克拉拉细胞的可能性。我们建立了一种新的简单方法,通过机械和酶解的组合分离表达 CCSP 的细胞——克拉拉细胞,然后使用流式细胞术分选技术。我们表明,整个肺的分离细胞中约有 25%表达 CCSP。在得到的制剂中,高达 98%的细胞表达 CCSP。值得注意的是,我们发现包括 CD44、CD133、Sca-1 和 Sox2 在内的几种常见的干细胞标志物在 CCSP(+)细胞中表达。此外,CCSP(+)细胞能够在体外形成具有 0.97‰效率的球体集落。体内平行研究证实,小鼠气道中 CCSP(-)表达细胞的一小部分也表现出干细胞样特性,如标记保留和在终末细支气管 (TB) 中含有稀有支气管肺泡干细胞 (BASCs)。我们得出结论,CCSP(+)细胞表现出多种干细胞样特征,包括干细胞标志物表达、类器官集落形成和自我更新能力。通过流式细胞术分选分离克拉拉细胞是研究原代克拉拉细胞在干细胞研究和小鼠模型中的功能的有用方法。