An injury-induced mesenchymal-epithelial cell niche coordinates regenerative responses in the lung

Severe lung injury causes airway basal stem cells to migrate and outcompete alveolar stem cells, resulting in dysplastic repair. We found that this "stem cell collision" generates an injury-induced tissue niche containing keratin 5<sup>+</sup> epithelial cells and plastic Pdgfra<sup>+</sup> mesenchymal cells. Single-cell analysis revealed that the injury-induced niche is governed by mesenchymal proliferation and Notch signaling, which suppressed Wnt/Fgf signaling in the injured niche. Conversely, loss of Notch signaling rewired alveolar signaling patterns to promote functional regeneration and gas exchange. Signaling patterns in injury-induced niches can differentiate fibrotic from degenerative human lung diseases through altering the direction of Wnt/Fgf signaling. Thus, we have identified an injury-induced niche in the lung with the ability to discriminate human lung disease phenotypes.

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Publication Details

Journal
Science
Published
2024-12-12
DOI
https://doi.org/10.1126/science.ado5561
Citations
44
Primary Topic
Neonatal Respiratory Health Research
Type
article
Field-Weighted Citation Impact
18.01
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article

An injury-induced mesenchymal-epithelial cell niche coordinates regenerative responses in the lung

Edward Cantu, Andrew E. Vaughan, Chen Shen, Yun Ying et al.
44 citations
Science
Neonatal Respiratory Health Research
18.01
article

An injury-induced mesenchymal-epithelial cell niche coordinates regenerative responses in the lung

Edward Cantu, Andrew E. Vaughan, Chen Shen, Yun Ying, Joshua M. Diamond, L. Raposo Rodríguez, Gan Zhao, Mijeong Kim, Fabian L. Cardenas‐Diaz, Ullas V. Chembazhi, Ana N. Nottingham, Shanru Li, Maria C. Basil, Edward E. Morrisey, Susan M. Lin, Dakota L. Jones, Michael P. Morley, Su Zhou, Sarah E. Schaefer, Xinyuan Li
article en
44 citations

Abstract

Severe lung injury causes airway basal stem cells to migrate and outcompete alveolar stem cells, resulting in dysplastic repair. We found that this "stem cell collision" generates an injury-induced tissue niche containing keratin 5<sup>+</sup> epithelial cells and plastic Pdgfra<sup>+</sup> mesenchymal cells. Single-cell analysis revealed that the injury-induced niche is governed by mesenchymal proliferation and Notch signaling, which suppressed Wnt/Fgf signaling in the injured niche. Conversely, loss of Notch signaling rewired alveolar signaling patterns to promote functional regeneration and gas exchange. Signaling patterns in injury-induced niches can differentiate fibrotic from degenerative human lung diseases through altering the direction of Wnt/Fgf signaling. Thus, we have identified an injury-induced niche in the lung with the ability to discriminate human lung disease phenotypes.

ScienceVol. 386(6727)
Penn Center for AIDS Research (US), University of Pennsylvania (US)
Reduced inequalities
Openalex Percentile: Top 0%
Neonatal Respiratory Health Research
18.01
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