Hypercapnia modulates cAMP signalling and cystic fibrosis transmembrane conductance regulator-dependent anion and fluid secretion in airway epithelia

J Physiol. 2016 Mar 15;594(6):1643-61. doi: 10.1113/JP271309. Epub 2015 Dec 20.

Abstract

Hypercapnia is clinically defined as an arterial blood partial pressure of CO2 of above 40 mmHg and is a feature of chronic lung disease. In previous studies we have demonstrated that hypercapnia modulates agonist-stimulated cAMP levels through effects on transmembrane adenylyl cyclase activity. In the airways, cAMP is known to regulate cystic fibrosis transmembrane conductance regulator (CFTR)-mediated anion and fluid secretion, which contributes to airway surface liquid homeostasis. The aim of the current work was to investigate if hypercapnia could modulate cAMP-regulated ion and fluid transport in human airway epithelial cells. We found that acute exposure to hypercapnia significantly reduced forskolin-stimulated elevations in intracellular cAMP as well as both adenosine- and forskolin-stimulated increases in CFTR-dependent transepithelial short-circuit current, in polarised cultures of Calu-3 human airway cells. This CO2 -induced reduction in anion secretion was not due to a decrease in HCO3 (-) transport given that neither a change in CFTR-dependent HCO3 (-) efflux nor Na(+) /HCO3 (-) cotransporter-dependent HCO3 (-) influx were CO2 -sensitive. Hypercapnia also reduced the volume of forskolin-stimulated fluid secretion over 24 h, yet had no effect on the HCO3 (-) content of the secreted fluid. Our data reveal that hypercapnia reduces CFTR-dependent, electrogenic Cl(-) and fluid secretion, but not CFTR-dependent HCO3 (-) secretion, which highlights a differential sensitivity of Cl(-) and HCO3 (-) transporters to raised CO2 in Calu-3 cells. Hypercapnia also reduced forskolin-stimulated CFTR-dependent anion secretion in primary human airway epithelia. Based on current models of airways biology, a reduction in fluid secretion, associated with hypercapnia, would be predicted to have important consequences for airways hydration and the innate defence mechanisms of the lungs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bicarbonates / metabolism*
  • Carbon Dioxide / metabolism*
  • Cell Line
  • Cells, Cultured
  • Chlorides / metabolism*
  • Cyclic AMP / metabolism*
  • Cystic Fibrosis Transmembrane Conductance Regulator / metabolism*
  • Humans
  • Hypercapnia / metabolism*
  • Ion Transport
  • Respiratory Mucosa / metabolism*
  • Signal Transduction
  • Sodium / metabolism

Substances

  • Bicarbonates
  • Chlorides
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Carbon Dioxide
  • Sodium
  • Cyclic AMP