Conchola, Ansley SFrum, TristanXiao, ZhiweiHsu, Peggy PKaur, KamikaDowney, Michael SHein, Renee FCMiller, Alyssa JTsai, Yu-HwaiWu, AngelineHolloway, Emily MAnand, AbhinavMurthy, Preetish Kadur LakshminarasimhaGlass, IanTata, Purushothama RSpence, Jason R2023-10-012023-10-012023-060027-84241091-6490https://hdl.handle.net/10161/29039Using scRNA-seq and microscopy, we describe a cell that is enriched in the lower airways of the developing human lung and identified by the unique coexpression of <i>SCGB3A2/SFTPB/CFTR</i>. To functionally interrogate these cells, we apply a single-cell barcode-based lineage tracing method, called CellTagging, to track the fate of <i>SCGB3A2/SFTPB/CFTR</i> cells during airway organoid differentiation in vitro. Lineage tracing reveals that these cells have a distinct differentiation potential from basal cells, giving rise predominantly to pulmonary neuroendocrine cells and a subset of multiciliated cells distinguished by high <i>C6</i> and low <i>MUC16</i> expression. Lineage tracing results are supported by studies using organoids and isolated cells from the lower noncartilaginous airway. We conclude that <i>SCGB3A2/SFTPB/CFTR</i> cells are enriched in the lower airways of the developing human lung and contribute to the epithelial diversity and heterogeneity in this region.LungOrganoidsEpithelial CellsStem CellsHumansCystic Fibrosis Transmembrane Conductance RegulatorCell DifferentiationCell LineageRegionally distinct progenitor cells in the lower airway give rise to neuroendocrine and multiciliated cells in the developing human lung.Journal article2023-10-01