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Alveolar Type II Cell-derived MMP1 <sup>high</sup> basal cells promote destructive microcysts in idiopathic pulmonary fibrosis

2025-12-11

Abstract excerpt

Idiopathic Pulmonary Fibrosis (IPF) is a fatal lung disease characterized by progressive epithelial metaplasia and widespread fibrosis. Alveolar microcysts develop near terminal airways in IPF and are linked to poor outcome. Using HTII-280 as a short-term lineage marker of AT2-derived AT0 (SFTPC + /SCGB3A2 + ) and basaloid (KRT17⁺) cells, together with organoids and spatial transcriptomics (Xenium), we highlight...

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Literature Corpus work
e1777eb1-0a14-5895-90ef-ec4fe37d2c6c
DOI
10.64898/2025.12.08.693033
Open publication

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Alveolar Type II Cell-derived MMP1 <sup>high</sup> basal cells promote destructive microcysts in idiopathic pulmonary fibrosisDOI 10.64898/2025.12.08.693033
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