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Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis
Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis
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Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis
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Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis
Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis

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Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis
Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis
Journal Article

Lung extracellular matrix modulates KRT5+ basal cell activity in pulmonary fibrosis

2023
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Overview
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. Idiopathic pulmonary fibrosis has been associated with aberrant expansion of KRT5-expressing basal cells. Here the authors show how changes in the ECM glycoprotein SPARC restrict the movement of KRT5+ cells, affecting their retention within fibrotic tissue.