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• W4311854915 abstract "Abstract Aberrant expansion of KRT5 + basal cells in the distal lung accompanies progressive alveolar epithelial cell loss and tissue remodelling during fibrogenesis in idiopathic pulmonary fibrosis (IPF). The mechanisms determining activity of KRT5 + cells in IPF have not been delineated. Here, we reveal a potential mechanism by which KRT5 + cells migrate within the fibrotic lung, navigating regional differences in collagen topography. In vitro , KRT5 + cell migratory characteristics and expression of remodelling genes are modulated by extracellular matrix (ECM) composition and organisation. Mass spectrometry-based proteomics revealed compositional differences in ECM components secreted by primary human lung fibroblasts (HLF) from IPF patients compared to controls. Over-expression of ECM glycoprotein, Secreted Protein Acidic and Cysteine Rich (SPARC) in the IPF HLF matrix restricts KRT5 + cell migration in vitro . Together, our findings demonstrate how changes to the ECM in IPF directly influence KRT5 + cell behaviour and function contributing to remodelling events in the fibrotic niche." @default.
• W4311854915 created "2023-01-01" @default.
• W4311854915 creator A5002341522 @default.
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• W4311854915 date "2022-12-18" @default.
• W4311854915 modified "2023-10-14" @default.
• W4311854915 title "Lung extracellular matrix modulates KRT5⁺basal cell activity in pulmonary fibrosis" @default.
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• W4311854915 doi "https://doi.org/10.1101/2022.12.16.520808" @default.
• W4311854915 hasPublicationYear "2022" @default.
• W4311854915 type Work @default.
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