Résumé
Psoriasin is a low molecular weight Ca2+-binding protein with known antimicrobial activity. Since human airway epithelial cells produce a number of powerful antimicrobial agents as part of their host defence, we investigated whether psoriasin was expressed in human bronchial epithelial cell lines. Expression was investigated in 16HBE14o- cells, derived from a normal individual, and compared to CFBE41o- cells, derived from a cystic fibrosis patient. We also examined psoriasin expression following treatment with factors pertinent to the CF lung-oxidant stress and exposure to pro-inflammatory cytokines. CFBE41o- cells demonstrated much reduced psoriasin levels compared to the 16HBE14o- cells. Increased psoriasin expression was seen following treatment with IL-22 and a cytomix of the pro-inflammatory cytokines IL-1β, TNF-α and IFN-γ; however, the oxidant stressor tert-butyl hydroperoxide had no apparent effect. Over-expression of human psoriasin into both cell lines resulted in increased internalization of Pseudomonas aeruginosa. In conclusion, expression of psoriasin - which has known anti-microbial activity in other systems - appears to be reduced in CFBE410- compared to 16HBE14o- cells, and its expression modified by exposure to pro-inflammatory cytokines.
Langue d'origine | English |
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Pages (de-à) | 177-185 |
Nombre de pages | 9 |
Journal | Respiratory Physiology and Neurobiology |
Volume | 183 |
Numéro de publication | 3 |
DOI | |
Statut de publication | Published - sept. 30 2012 |
Note bibliographique
Funding Information:We wish to thank Christina Jones for excellent technical assistance, Dr Eileen Denovan-Wright for assistance with the qPCR studies, Dr Andrew Stadnyk for critical reading of the manuscript, and Drs Tong-Jun Lin and Dr Nikhil Thomas for assistance with the P. aeruginosa work. This work was supported entirely by Cystic Fibrosis Canada.
ASJC Scopus Subject Areas
- General Neuroscience
- Physiology
- Pulmonary and Respiratory Medicine
PubMed: MeSH publication types
- Journal Article
- Research Support, Non-U.S. Gov't