RT Journal Article SR Electronic T1 Stable iPSC-derived NKX2-1+ Lung Bud Tip Progenitor Organoids Give Rise to Airway and Alveolar Cell Types JF bioRxiv FD Cold Spring Harbor Laboratory SP 2022.02.25.481981 DO 10.1101/2022.02.25.481981 A1 Hein, Renee F.C. A1 Conchola, Ansley S. A1 Fine, Alexis A1 Xiao, Zhiwei A1 Frum, Tristan A1 Childs, Charlie J. A1 Tsai, Yu-Hwai A1 Holloway, Emily M. A1 Huang, Sha A1 Mahoney, John A1 Spence, Jason R. YR 2022 UL http://biorxiv.org/content/early/2022/02/25/2022.02.25.481981.abstract AB Bud tip progenitors (BTPs) in the developing lung give rise to all epithelial cell types found in the airways and alveoli. The current work aimed to develop an iPSC organoid model enriched with stable NKX2-1+ BTP-like cells. Building on prior work, we optimized a directed differentiation paradigm to generate spheroids with robust NKX2-1 expression. Spheroids were expanded into organoids that possessed NKX2-1+/CPM+ BTP-like cells, which increased in number over time. Single cell RNA-sequencing analysis revealed a high degree of transcriptional similarity between induced BTPs (iBTPs) and in vivo BTPs. Using FACS, iBTPs can be purified and expanded as induced bud tip organoids (iBTO), which maintain an enriched population of bud tip progenitors. When iBTOs are directed to differentiate into airway or alveolar cell types using well-established methods, they give rise to organoids composed of organized airway or alveolar epithelium, respectively. Collectively, iBTOs are transcriptionally and functionally similar to in vivo BTPs, providing an important model to study human lung development and differentiation.SUMMARY STATEMENT iPSC-derived lung bud tip progenitors emerge in organoid culture, can be isolated and expanded, are transcriptionally similar to primary bud tip progenitors, and can differentiate into airway or alveolar organoids.Competing Interest StatementJRS holds intellectual property pertaining to lung organoid technologies.