Journal
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
Volume 163, Issue 3, Pages 737-744Publisher
AMER THORACIC SOC
DOI: 10.1164/ajrccm.163.3.2002117
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- NHLBI NIH HHS [1RO1 HL60913-01, 1RO1 HL60195-01] Funding Source: Medline
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Emphysema due to cigarette smoking is characterized by a loss of alveolar structures. We hypothesize that the disappearance of alveoli involves apoptosis of septal endothelial cells and a decreased expression of lung vascular endothelial growth factor (VEGF) and its receptor 2 (VEGF R2). By terminal transferase dUTP nick end labeling (TUNEL) in combination with immunohistochemistry, we found that the number of TUNEL+ septal epithelial and endothelial cells/lung tissue nucleic acid (mug) was increased in the alveolar septa of emphysema lungs (14.2 +/- 2.0/mug, n = 6) when compared with normal lungs (6.8 +/- 1.3/mug, n = 7) (p < 0.01) and with primary pulmonary hypertensive lungs (2.3 +/- 0.8/mug, n = 5) (p < 0.001). The cell death events were not significantly different between healthy nonsmoker (7.4 +/- 1.9/mug) and smoker (5.7 +/- 0.7/mug) control subjects. The TUNEL results were confirmed by single-stranded DNA and active caspase-3 immunohistochemistry, and by DNA ligation assay. Emphysema lungs (n = 12) had increased levels of oligonucleosomal-length DNA fragmentation when compared with normal lungs (n = 11). VEGF, VEGF R2 protein, and mRNA expression were significantly reduced in emphysema. We propose that epithelial and endothelial alveolar septal death due to a decrease of endothelial cell maintenance factors may be part of the pathogenesis of emphysema.
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