Early human fetal lung atlas reveals the temporal dynamics of epithelial cell plasticity.
Henry QuachSpencer FarrellMing Jia Michael WuKayshani KanagarajahJoseph Wai-Hin LeungXiaoqiao XuPrajkta KallurkarAndrei L TurinskyChristine E BearFelix RatjenBrian KalishSidhartha GoyalTheo J MoraesAmy P WongPublished in: Nature communications (2024)
Studying human fetal lungs can inform how developmental defects and disease states alter the function of the lungs. Here, we sequenced >150,000 single cells from 19 healthy human pseudoglandular fetal lung tissues ranging between gestational weeks 10-19. We capture dynamic developmental trajectories from progenitor cells that express abundant levels of the cystic fibrosis conductance transmembrane regulator (CFTR). These cells give rise to multiple specialized epithelial cell types. Combined with spatial transcriptomics, we show temporal regulation of key signalling pathways that may drive the temporal and spatial emergence of specialized epithelial cells including ciliated and pulmonary neuroendocrine cells. Finally, we show that human pluripotent stem cell-derived fetal lung models contain CFTR-expressing progenitor cells that capture similar lineage developmental trajectories as identified in the native tissue. Overall, this study provides a comprehensive single-cell atlas of the developing human lung, outlining the temporal and spatial complexities of cell lineage development and benchmarks fetal lung cultures from human pluripotent stem cell differentiations to similar developmental window.
Keyphrases
- single cell
- endothelial cells
- cystic fibrosis
- stem cells
- induced pluripotent stem cells
- pluripotent stem cells
- depressive symptoms
- palliative care
- pregnant women
- gene expression
- pseudomonas aeruginosa
- transcription factor
- pulmonary hypertension
- signaling pathway
- mesenchymal stem cells
- chronic obstructive pulmonary disease
- cell death
- bone marrow
- preterm birth
- weight loss