Glucocorticoids Distinctively Modulate the CFTR Channel with Possible Implications in Lung Development and Transition into Extrauterine Life

• Published in: PloS one Vol. 10; no. 4; p. e0124833
• Main Authors: Laube, Mandy, Bossmann, Miriam, Thome, Ulrich H
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 24.04.2015; Public Library of Science (PLoS)
• Subjects: Alveolar Epithelial Cells - drug effects; Alveolar Epithelial Cells - metabolism; Alveoli; Animals; Cell Line; Channel gating; Chloride channels; Chloride Channels - genetics; Chloride Channels - metabolism; Chloride ions; Chloride transport; Cortisol; Cystic fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator - genetics; Cystic Fibrosis Transmembrane Conductance Regulator - metabolism; Dexamethasone - pharmacology; Dose-Response Relationship, Drug; Fetal development; Fetuses; Gene Expression; Gene Expression Regulation - drug effects; Gestation; Glucocorticoids; Glucocorticoids - metabolism; Glucocorticoids - pharmacology; Hormones; Humans; Ion channels; Kinases; Lung - embryology; Lung - metabolism; Lungs; Mifepristone; Models, Animal; Organogenesis - genetics; Pediatrics; Physiological effects; Pregnancy; Proteins; Rats; Respiratory Mucosa - drug effects; Respiratory Mucosa - metabolism; Respiratory tract; RNA; RNA, Messenger - genetics; Rodents; Secretion; Sodium channels; Steroids (Organic compounds); Teenagers; Germany
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0124833

During fetal development, the lung is filled with fluid that is secreted by an active Cl- transport promoting lung growth. The basolateral Na+,K+,2Cl- cotransporter (NKCC1) participates in Cl- secretion. The apical Cl- channels responsible for secretion are unknown but studies suggest an involvement of the cystic fibrosis transmembrane conductance regulator (CFTR). CFTR is developmentally regulated with a high expression in early fetal development and a decline in late gestation. Perinatal lung transition is triggered by hormones that stimulate alveolar Na+ channels resulting in fluid absorption. Little is known on how hormones affect pulmonary Cl- channels. Since the rise of fetal cortisol levels correlates with the decrease in fetal CFTR expression, a causal relation may be assumed. The aim of this study was to analyze the influence of glucocorticoids on pulmonary Cl- channels. Alveolar cells from fetal and adult rats, A549 cells, bronchial Calu-3 and 16HBE14o- cells, and primary rat airway cells were studied with real-time quantitative PCR and Ussing chambers. In fetal and adult alveolar cells, glucocorticoids strongly reduced Cftr expression and channel activity, which was prevented by mifepristone. In bronchial and primary airway cells CFTR mRNA expression was also reduced, whereas channel activity was increased which was prevented by LY-294002 in Calu-3 cells. Therefore, glucocorticoids strongly reduce CFTR expression while their effect on CFTR activity depends on the physiological function of the cells. Another apical Cl- channel, anoctamin 1 showed a glucocorticoid-induced reduction of mRNA expression in alveolar cells and an increase in bronchial cells. Furthermore, voltage-gated chloride channel 5 and anoctamine 6 mRNA expression were increased in alveolar cells. NKCC1 expression was reduced by glucocorticoids in alveolar and bronchial cells alike. The results demonstrate that glucocorticoids differentially modulate pulmonary Cl- channels and are likely causing the decline of CFTR during late gestation in preparation for perinatal lung transition.