Lung Biology Center.
Cardiovascular Research Institute.
Am J Respir Cell Mol Biol. 2021 Mar;64(3):308-317. doi: 10.1165/rcmb.2020-0149MA.
The human airway epithelium is essential in homeostasis, and epithelial dysfunction contributes to chronic airway disease. Development of flow-cytometric methods to characterize subsets of airway epithelial cells will enable further dissection of airway epithelial biology. Leveraging single-cell RNA-sequencing data in combination with known cell type-specific markers, we developed panels of antibodies to characterize and isolate the major airway epithelial subsets (basal, ciliated, and secretory cells) from human bronchial epithelial-cell cultures. We also identified molecularly distinct subpopulations of secretory cells and demonstrated cell subset-specific expression of low-abundance transcripts and microRNAs that are challenging to analyze with current single-cell RNA-sequencing methods. These new tools will be valuable for analyzing and separating airway epithelial subsets and interrogating airway epithelial biology.
人类气道上皮细胞在维持内环境稳定中至关重要,而上皮细胞功能障碍会导致慢性气道疾病。开发流式细胞术方法来鉴定气道上皮细胞亚群将有助于进一步解析气道上皮生物学。我们利用单细胞 RNA 测序数据并结合已知的细胞类型特异性标记物,开发了一系列抗体,以鉴定和分离人支气管上皮细胞培养物中的主要气道上皮细胞亚群(基底细胞、纤毛细胞和分泌细胞)。我们还鉴定了分泌细胞的分子上不同的亚群,并证明了低丰度转录本和 microRNA 的细胞亚群特异性表达,这些在使用当前的单细胞 RNA 测序方法时很难分析。这些新工具对于分析和分离气道上皮细胞亚群以及研究气道上皮生物学将非常有价值。