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bioRxiv · 10.1101/2024.12.10.627749

Multiscale single-cell assessment of the fibrotic niche in idiopathic pulmonary fibrosis

Liu, B.·Stewart, I.·May, J.·Zarcone, M. C.·Lopez-Jimenez, E.·Lambie, N.·Matthews, N.·Johnson, S. R.·Tatler, A. L.·Hewitt, R.·Wain, L. V.·Clifford, R. L.·Renzoni, E. A.·George, P. M.·Wells, A. U.·Reed, A. K.·Jenkins, R. G.·JOHN, A. E.
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Abstract

BackgroundIdiopathic pulmonary fibrosis (IPF) is a progressive, fatal disease characterised by excessive extracellular matrix deposition within the lung. Recent advances in single-cell RNA sequencing have identified distinct fibrotic populations, yet their origins and spatial relationships remain incompletely understood. MethodsUsing spatial transcriptomics and Hyperion imaging mass cytometry we compared the cellular composition in formalin fixed paraffin embedded fibrotic lesions (n=9 patients) with control lung (n=9), and cellular interactions were inferred using CellChat V2 ligand-receptor analysis. Monolayers of airway epithelial cells were used to identify changes in keratin (KRT) expression following cell detachment and cyclical mechanical stretch. ResultsSpatial multiomics profiling of human lung cells confirmed the in situ localisation of previously described IPF-enriched populations, and identified a previously unrecognized KRT5low/KRT17 epithelial population derived from airway basal cells that progressively acquiring molecular features of aberrant basaloid cells, forming a unique fibrotic niche enriched with the Secreted Phosphoprotein 1 (SPP1) positive macrophages. Functional studies demonstrated that epithelial detachment and cyclical mechanical stretch drive KRT5 reduction, providing a mechanism for the emergence of this transitional state. In addition, we also identified distinct immune-stromal niches enriched in lymphocytes and alveolar fibroblasts. ConclusionThese findings delineate distinct fibrotic epithelial niches in IPF and support a model in which epithelial loss induces aberrant basaloid differentiation and fibroblast activation, with subsequent airway traction and epithelial detachment generating a secondary niche enriched in basal-derived KRT5low/KRT17 cells and SPP1 macrophages.

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Liu, B., Stewart, I., May, J., Zarcone, M. C., Lopez-Jimenez, E., Lambie, N., Matthews, N., Johnson, S. R., Tatler, A. L., Hewitt, R., Wain, L. V., Clifford, R. L., Renzoni, E. A., George, P. M., Wells, A. U., Reed, A. K., Jenkins, R. G., JOHN, A. E.. 2024-12-12. Multiscale single-cell assessment of the fibrotic niche in idiopathic pulmonary fibrosis. https://doi.org/10.1101/2024.12.10.627749

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