Regionally distinct progenitor cells in the lower airway give rise to neuroendocrine and multiciliated cells in the developing human lung

Author:

Conchola Ansley S.1ORCID,Frum Tristan2ORCID,Xiao Zhiwei2,Hsu Peggy P.23,Kaur Kamika2,Downey Michael S.23ORCID,Hein Renee F. C.4ORCID,Miller Alyssa J.1,Tsai Yu-Hwai2,Wu Angeline2,Holloway Emily M.4,Anand Abhinav2,Murthy Preetish Kadur Lakshminarasimha5,Glass Ian6,Tata Purushothama R.7ORCID,Spence Jason R.1234

Affiliation:

1. Graduate Program in Cellular and Molecular Biology, University of Michigan Medical School, Ann Arbor, MI 48109

2. Department of Internal Medicine, Division of Gastroenterology and Hepatology, University of Michigan Medical School, Ann Arbor, MI 48109

3. Rogel Cancer Center, University of Michigan Medical School, Ann Arbor, MI 48109

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

5. Department of Pharmacology and Regenerative Medicine, University of Illinois Chicago, IL 60607

6. Department of Pediatrics, Genetic Medicine, University of Washington, Seattle, WA 98195

7. Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710

Abstract

Using 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 SCGB3A2/SFTPB/CFTR . To functionally interrogate these cells, we apply a single-cell barcode-based lineage tracing method, called CellTagging, to track the fate of SCGB3A2/SFTPB/CFTR 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 C6 and low MUC16 expression. Lineage tracing results are supported by studies using organoids and isolated cells from the lower noncartilaginous airway. We conclude that SCGB3A2/SFTPB/CFTR cells are enriched in the lower airways of the developing human lung and contribute to the epithelial diversity and heterogeneity in this region.

Funder

Chan Zuckerberg Initiative

HHS | NIH | National Heart, Lung, and Blood Institute

HHS | NIH | National Institute of Dental and Craniofacial Research

HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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