bioRxivCell Biology
Identification a novel subset of alveolar type 2 cells expanding following pneumonectomy and enriched in PD-L1
N. Ahmadvand, F. Khosravi, A. Lingampally, R. M. Wasnick, A. I. Vazquez-Armendariz, M. Heiner, S. Rivetti, Y. Lv, J. Wilhelm, A. Gunther, S. Herold, D. M. Al Alam, C. Chen, P. Minoo, J. Zhang, S. Bellusci
Abstract
Alveolar type 2 (AT2) cells are heterogeneous cells; where specialized AT2 subpopulations within this lineage exhibit stem cell properties. However, the existence of quiescent, immature cells within the AT2 lineage, which get activated during lung regeneration, is unknown. SftpcCreERT2/+; tdTomatoflox/flox mice were used for the labelling of AT2 cells and labeled subpopulations were analyzed by flow cytometry, qPCR, ATAC-seq, gene arrays, pneumonectomy, and culture of precision-cut lung slides. Human lungs from donor and IPF were also analyzed. In mice, we detected two distinct AT2 subpopulations with low tdTomato level (TomLow) and high tdTomato level (TomHigh). TomLow express lower level of AT2 differentiation markers, Fgfr2b and Etv5, while TomHigh, as bona fide mature AT2 cells, show higher level of Sftpc, Sftpb, Sftpa1, Fgfr2b, and Etv5. ATAC-seq analysis indicates that TomLow and TomHigh constitute two distinct cell populations with specific silencing of Sftpc, Rosa26 and cell cycle gene loci in TomLow. Upon pneumonectomy, TomLow but not TomHigh cells proliferate and upregulate the expression of Fgfr2b, Etv5, Sftpc, Ccnd1 and Ccnd2 compared to sham. TomLow cells overexpress PD-L1, an immune inhibitory membrane receptor ligand, which is used by flow cytometry to differentially isolate these two sub-populations. In the human lung, PD-L1 and HTII-280 antibodies are used by flow cytometry to differentially sort mature AT2 (HTII-280-high, PD-L1-low) as well as an additional subpopulation of epithelial cells characterized by HTII-280-Low and PD-L1-high. We have identified a novel population of AT2 quiescent immature progenitor cells in mouse that proliferate upon pneumonectomy and provided evidence for the existence of such cells in human. Significance of the workThe characterization and mechanism of the proliferation of a novel and relevant pool of AT2 progenitor cells for the repair/regeneration process after injury are critical to improving respiratory function in patients with lung disease.
- organism: mouse
- organism: human
- assay: flow cytometry
- assay: ATAC-seq
- assay: bulk RNA-seq
- research focus: cell type annotation
- approach: experimental assay
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Cell-surface PD-L1 expression identifies a sub-population of distal epithelial cells enriched in idiopathic pulmonary fibrosis
N. Ahmadvand, G. Carraro, … C. Ruppert·bioRxiv·Mar 9, 2022
- Co-optation of the regenerative role of type 2 alveolar cells in distal lung repair in mice by terminal airway epithelial cells in humans
Juan Antonio Torres, Elisabeth Schonweiler, … Hans‐Willem Snoeck·bioRxiv·Jul 28, 2026
- Temporal and spatial staging of lung alveolar regeneration is determined by the grainyhead transcription factor Tfcp2l1
F. L. Cardenas-Diaz, D. C. Liberti, … E. E. Morrisey·bioRxiv·Aug 23, 2022
- Immortalized AT2 Cell Lines from Healthy and IPF Lungs Enable 2D and 3D Cultures
Anas Rabata, Yujie Qiao, … Dianhua Jiang·bioRxiv·Mar 9, 2026
- Fgfr2b signaling is essential for the maintenance of the alveolar epithelial type 2 lineage during lung homeostasis in mice
Negah Ahmadvand, Arun Lingampally, … Savério Bellusci·Cellular and Molecular Life SciencesPeer-reviewed·May 19, 2022
- Isolation, omics characterization and organotypic culture of alveolar type II pulmonary epithelial cells
H. Li, M. Schuette, … A. Ploubidou·bioRxiv·Aug 19, 2021