Details

Autor(en) / Beteiligte

• Tondelier, Danielle
• Brouillard, Franck
• Lipecka, Joanna
• Labarthe, Régis
• Bali, Moëz
• De Beauregard, Marie-Ayliette Costa
• Torossi, Tanja
• Cougnon, Marc
• Edelman, Aleksander
• Baudouin-Legros, Maryvonne

Titel

Aspirin and some other nonsteroidal anti-inflammatory drugs inhibit cystic fibrosis transmembrane conductance regulator protein gene expression in T-84 cells

Ist Teil von

• Mediators of Inflammation, 1999-01, Vol.1999 (4-5), p.219-227

Ort / Verlag

United States: Hindawi Limiteds

Erscheinungsjahr

1999

Quelle

MEDLINE

Beschreibungen/Notizen

• CYSTIC fibrosis (CF) is caused by mutations in the CF gene, which encodes CF transmembrane conductance regulator protein (CFTR), a transmembrane protein that acts as a cAMP-regulated chloride channel. The disease is characterized by inflammation but the relationship between inflammation, abnormal transepithelial ion transport, and the clinical manifestations of CF are uncertain. The present study was undertaken to determine whether three nonsteroidal anti-inflammatory drugs (NSAIDs) (aspirin, ibuprofen, and indomethacin) modulate CFTR gene expression in T-84 cells. Treatment with NSAIDs reduced CFTR transcripts, and decreased cAMP-stimulated anion fluxes, an index of CFTR function. However, the two phenomena occurred at different concentrations of both drugs. The results indicate that NSAIDs can regulate both CFTR gene expression and the function of CFTR-related chloride transport, and suggest that NSAIDs act via multiple transduction pathways.