Stable iPSC-derived NKX2-1+ lung bud tip progenitor organoids give rise to airway and alveolar cell types

Author:

Hein Renee F. C.12ORCID,Conchola Ansley S.3ORCID,Fine Alexis S.4,Xiao Zhiwei4,Frum Tristan4ORCID,Brastrom Lindy K.4,Akinwale Mayowa A.1,Childs Charlie J.12ORCID,Tsai Yu-Hwai4,Holloway Emily M.1,Huang Sha4,Mahoney John5ORCID,Heemskerk Idse12ORCID,Spence Jason R.1346ORCID

Affiliation:

1. University of Michigan Medical School 1 Department of Cell and Developmental Biology , , Ann Arbor, MI 48109, USA

2. University of Michigan Medical School 2 Department of Computational Medicine and Bioinformatics , , Ann Arbor, MI 48109, USA

3. University of Michigan Medical School 3 Program in Cell and Molecular Biology , , Ann Arbor, MI 48109, USA

4. University of Michigan Medical School 4 Department of Internal Medicine , , Ann Arbor, MI 48109, USA

5. Cystic Fibrosis Foundation 5 Therapeutics Lab , , Lexington, MA 02421, USA

6. University of Michigan Medical School 6 Department of Biomedical Engineering Medicine , , Ann Arbor, MI 48109, USA

Abstract

ABSTRACT Bud tip progenitors (BTPs) in the developing lung give rise to all epithelial cell types found in the airways and alveoli. This work aimed to develop an iPSC organoid model enriched with NKX2-1+ BTP-like cells. Building on previous studies, we optimized a directed differentiation paradigm to generate spheroids with more 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 were purified and expanded as induced bud tip progenitor organoids (iBTOs), which maintained an enriched population of bud tip progenitors. When iBTOs were directed to differentiate into airway or alveolar cell types using well-established methods, they gave 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 for studying human lung development and differentiation.

Funder

Chan Zuckerberg Initiative

National Heart, Lung, and Blood Institute

National Institutes of Health

University of Michigan Medical School

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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