A single-cell, time-resolved profiling of Xenopus mucociliary epithelium reveals nonhierarchical model of development

Author:

Lee Julie1ORCID,Møller Andreas Fønss23ORCID,Chae Shinhyeok4ORCID,Bussek Alexandra1,Park Tae Joo5ORCID,Kim Youni6,Lee Hyun-Shik6,Pers Tune H.7ORCID,Kwon Taejoon48ORCID,Sedzinski Jakub1ORCID,Natarajan Kedar Nath29ORCID

Affiliation:

1. The Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, Copenhagen, Denmark.

2. Danish Institute of Advanced Study (DIAS) and Functional Genomics and Metabolism Research Unit, University of Southern Denmark, Odense, Denmark.

3. Sino-Danish College (SDC), University of Chinese Academy of Sciences, Beijing, China.

4. Department of Biomedical Engineering, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea.

5. Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea.

6. KNU-Center for Nonlinear Dynamics, School of Life Sciences, BK21 FOUR KNU Creative BioResearch Group, College of Natural Sciences, Kyungpook National University, Daegu 41566, Republic of Korea.

7. The Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Blegdamsvej 3B, 2200 Copenhagen, Denmark.

8. Center for Genomic Integrity, Institute for Basic Science (IBS), Ulsan 44919, Republic of Korea.

9. DTU Bioengineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.

Abstract

The specialized cell types of the mucociliary epithelium (MCE) lining the respiratory tract enable continuous airway clearing, with its defects leading to chronic respiratory diseases. The molecular mechanisms driving cell fate acquisition and temporal specialization during mucociliary epithelial development remain largely unknown. Here, we profile the developing Xenopus MCE from pluripotent to mature stages by single-cell transcriptomics, identifying multipotent early epithelial progenitors that execute multilineage cues before specializing into late-stage ionocytes and goblet and basal cells. Combining in silico lineage inference, in situ hybridization, and single-cell multiplexed RNA imaging, we capture the initial bifurcation into early epithelial and multiciliated progenitors and chart cell type emergence and fate progression into specialized cell types. Comparative analysis of nine airway atlases reveals an evolutionary conserved transcriptional module in ciliated cells, whereas secretory and basal types execute distinct function-specific programs across vertebrates. We uncover a continuous nonhierarchical model of MCE development alongside a data resource for understanding respiratory biology.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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