Tondelier D, Brouillard F, Lipecka J, Labarthe R, Bali M, Costa de Beauregard M A, Torossi T, Cougnon M, Edelman A, Baudouin-Legros M
INSERM U. 467, Faculté de Médecine Necker-Enfants Malades, Paris, France.
Mediators Inflamm. 1999;8(4-5):219-27. doi: 10.1080/09629359990388.
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.
囊性纤维化(CF)由CF基因突变引起,该基因编码CF跨膜电导调节蛋白(CFTR),CFTR是一种作为cAMP调节氯离子通道的跨膜蛋白。该疾病的特征为炎症,但炎症、异常跨上皮离子转运与CF临床表现之间的关系尚不确定。本研究旨在确定三种非甾体抗炎药(NSAIDs)(阿司匹林、布洛芬和吲哚美辛)是否调节T-84细胞中的CFTR基因表达。NSAIDs处理可降低CFTR转录本,并减少cAMP刺激的阴离子通量,这是CFTR功能的一个指标。然而,这两种现象在两种药物的不同浓度下出现。结果表明,NSAIDs可调节CFTR基因表达及与CFTR相关的氯离子转运功能,并提示NSAIDs通过多种转导途径发挥作用。