Lack of inducible nitric oxide synthase in bronchial epithelium: a possible mechanism of susceptibility to infection in cystic fibrosis

Cystic fibrosis (CF) is an inherited disorder associated with severe inflammation and repeated bacterial infection and colonization in the lung. Airway epithelium is involved in defence against bacteria, but this system may be defective in CF. Pro‐inflammatory cytokines can stimulate the expression...

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Veröffentlicht in:The Journal of pathology 1998-03, Vol.184 (3), p.323-331
Hauptverfasser: Meng, Qing-Hai, Springall, David R., Bishop, Anne E., Morgan, Kevin, Evans, Tom J., Habib, Said, Gruenert, Dieter C., Gyi, Khin M., Hodson, Margaret E., Yacoub, Magdi H., Polak, Julia M.
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Sprache:eng
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Zusammenfassung:Cystic fibrosis (CF) is an inherited disorder associated with severe inflammation and repeated bacterial infection and colonization in the lung. Airway epithelium is involved in defence against bacteria, but this system may be defective in CF. Pro‐inflammatory cytokines can stimulate the expression of inducible nitric oxide synthase (iNOS), an enzyme generating nitric oxide, which functions as an important mediator in host defence mechanisms. To understand better the poor resistance to infections in the CF lung, the expression of the iNOS gene was investigated in explanted lungs from patients with cystic fibrosis (n‐13), bronchiectasis (n‐3), emphysema (n‐14), and in normal lungs (n‐8). In addition, bronchial epithelial cell lines were examined to study iNOS gene expression in vitro. Strong immunoreactivity for iNOS was seen in inflammatory cells and bronchial epithelium in all the diseased lungs, except for bronchial epithelium in CF. Quantitative analysis showed a significant reduction in the area of epithelium immunostained in CF [CF 6·8±1·6 (%±SEM); emphysema 18·2±2·8; normal 9·6±0·8, P
ISSN:0022-3417
1096-9896
DOI:10.1002/(SICI)1096-9896(199803)184:3<323::AID-PATH2>3.0.CO;2-2