Article
ACKR1-expressing venous endothelial cells establish a pro-fibrotic niche in pulmonary fibrosis
2026-08-03
Abstract excerpt
Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease characterized by excessive extracellular matrix deposition and irreversible architectural distortion of the lung. Fibrotic remodeling is driven by dynamic interactions among endothelial, fibroblast, epithelial and immune cells. Although pulmonary endothelial cells (ECs) are increasingly recognized as important contributors to IPF pathogenesis, the m...
Topics
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- Extracellular vesicles in disease
- IL-33, ST2, and ILC Pathways
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Medical Imaging and Pathology Studies
- Mesenchymal stem cell research
- Neonatal Respiratory Health Research
- Pulmonary Hypertension Research and Treatments
- Respiratory viral infections research
Identifiers and source
- Literature Corpus work
- 5e558de5-c83f-573a-afcb-eecfe5c4eda9
- DOI
- 10.64898/2026.07.31.742106
