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Fibronectin expression in bronchopulmonary dysplasia
R A Sinkin1, M Roberts, M B LoMonaco
1Department of Pediatrics (Neonatology), Children's Hospital at Strong, 601 Elmwood Avenue, Box 651, Rochester, NY 14642, USA.
Summary
Fibronectin (FN) is elevated in neonatal Bronchopulmonary dysplasia (BPD) lungs. Pulmonary cells, not airway epithelium, synthesize FN, with levels peaking during BPD
Area of Science:
- Neonatal lung disease
- Extracellular matrix biology
- Fibrosis research
Background:
- Bronchopulmonary dysplasia (BPD) is a chronic neonatal lung disease.
- Fibronectin (FN), an extracellular matrix protein, is elevated in BPD.
- Pulmonary FN originates from plasma and local synthesis.
Purpose of the Study:
- Identify pulmonary cells synthesizing FN.
- Quantify FN abundance in BPD lungs.
- Correlate FN levels with BPD stages.
Main Methods:
- In situ hybridization for FN mRNA.
- Immunohistochemistry for FN protein.
- Analysis of neonatal autopsy lung specimens (BPD vs. controls).
Main Results:
- FN mRNA and protein found in vascular endothelium, macrophages, fibroblasts, smooth muscle, and chondrocytes.
- Hyaline membranes showed intense FN protein staining.
- FN levels increased in early BPD, peaking in the chronic stage, and decreased in healed BPD.
Conclusions:
- Pulmonary cells, excluding airway epithelium, synthesize FN.
- Increased FN is associated with BPD progression and fibrotic changes.
- Pulmonary cell-derived FN plays a role in BPD pathogenesis.