Dagenais A, Denis C, Vives M F, Girouard S, Massé C, Nguyen T, Yamagata T, Grygorczyk C, Kothary R, Berthiaume Y
Département de Médecine, Centre Hospitalier de l'Université de Montréal-Hôtel-Dieu, Université de Montréal, Montreal, Quebec H2W 1T8, Canada.
Am J Physiol Lung Cell Mol Physiol. 2001 Jul;281(1):L217-30. doi: 10.1152/ajplung.2001.281.1.L217.
cAMP and dexamethasone are known to modulate Na+ transport in epithelial cells. We investigated whether dibutyryl cAMP (DBcAMP) and dexamethasone modulate the mRNA expression of two key elements of the Na+ transport system in isolated rat alveolar epithelial cells: alpha-, beta-, and gamma-subunits of the epithelial Na+ channel (ENaC) and the alpha1- and beta1-subunits of Na+-K+-ATPase. The cells were treated for up to 48 h with DBcAMP or dexamethasone to assess their long-term impact on the steady-state level of ENaC and Na+-K+-ATPase mRNA. DBcAMP induced a twofold transient increase of alpha-ENaC and alpha1-Na+-K+-ATPase mRNA that peaked after 8 h of treatment. It also upregulated beta- and gamma-ENaC mRNA but not beta1-Na+-K+-ATPase mRNA. Dexamethasone augmented alpha-ENaC mRNA expression 4.4-fold in cells treated for 24 h and also upregulated beta- and gamma-ENaC mRNA. There was a 1.6-fold increase at 8 h of beta1-Na+-K+-ATPase mRNA but no significant modulation of alpha1-Na+-K+-ATPase mRNA expression. Because DBcAMP and dexamethasone did not increase the stability of alpha-ENaC mRNA, we cloned 3.2 kb of the 5' sequences flanking the mouse alpha-ENaC gene to study the impact of DBcAMP and dexamethasone on alpha-ENaC promoter activity. The promoter was able to drive basal expression of the chloramphenicol acetyltransferase (CAT) reporter gene in A549 cells. Dexamethasone increased the activity of the promoter by a factor of 5.9. To complete the study, the physiological effects of DBcAMP and dexamethasone were investigated by measuring transepithelial current in treated and control cells. DBcAMP and dexamethasone modulated transepithelial current with a time course reminiscent of the profile observed for alpha-ENaC mRNA expression. DBcAMP had a greater impact on transepithelial current (2.5-fold increase at 8 h) than dexamethasone (1.8-fold increase at 24 h). These results suggest that modulation of alpha-ENaC and Na+-K+-ATPase gene expression is one of the mechanisms that regulates Na+ transport in alveolar epithelial cells.
已知环磷腺苷(cAMP)和地塞米松可调节上皮细胞中的钠离子转运。我们研究了二丁酰环磷腺苷(DBcAMP)和地塞米松是否能调节分离的大鼠肺泡上皮细胞中钠离子转运系统两个关键元件的mRNA表达:上皮钠离子通道(ENaC)的α、β和γ亚基以及钠钾ATP酶的α1和β1亚基。用DBcAMP或地塞米松处理细胞长达48小时,以评估它们对ENaC和钠钾ATP酶mRNA稳态水平的长期影响。DBcAMP诱导α-ENaC和α1-钠钾ATP酶mRNA瞬时增加两倍,在处理8小时后达到峰值。它还上调了β-和γ-ENaC mRNA,但未上调β1-钠钾ATP酶mRNA。地塞米松在处理24小时的细胞中使α-ENaC mRNA表达增加4.4倍,也上调了β-和γ-ENaC mRNA。β1-钠钾ATP酶mRNA在8小时时增加了1.6倍,但α1-钠钾ATP酶mRNA表达没有明显调节。由于DBcAMP和地塞米松没有增加α-ENaC mRNA的稳定性,我们克隆了小鼠α-ENaC基因侧翼的3.2 kb 5'序列,以研究DBcAMP和地塞米松对α-ENaC启动子活性的影响。该启动子能够驱动氯霉素乙酰转移酶(CAT)报告基因在A549细胞中的基础表达。地塞米松使启动子活性增加了5.9倍。为了完成该研究,通过测量处理过的细胞和对照细胞中的跨上皮电流,研究了DBcAMP和地塞米松的生理效应。DBcAMP和地塞米松调节跨上皮电流的时间进程让人想起α-ENaC mRNA表达所观察到的情况。DBcAMP对跨上皮电流的影响(8小时时增加了2.5倍)比对地塞米松的影响(24小时时增加了1.8倍)更大。这些结果表明,调节α-ENaC和钠钾ATP酶基因表达是调节肺泡上皮细胞中钠离子转运的机制之一。