Soluble adenylyl cyclase is localized to cilia and contributes to ciliary beat frequency regulation via production of cAMP

• Published in: The Journal of general physiology Vol. 130; no. 1; pp. 99 - 109
• Main Authors: Schmid, Andreas, Sutto, Zoltan, Nlend, Marie-Christine, Horvath, Gabor, Schmid, Nathalie, Buck, Jochen, Levin, Lonny R, Conner, Gregory E, Fregien, Nevis, Salathe, Matthias
• Format: Journal Article
• Language: English
• Published: United States Rockefeller University Press 01.07.2007; The Rockefeller University Press
• Subjects: Adenylyl Cyclases - metabolism; Carbon dioxide; Cells, Cultured; Cellular biology; Cilia - enzymology; Cilia - physiology; Cyclic AMP - metabolism; Epithelial Cells - metabolism; Gene expression; Humans; Inhibitor drugs; Lung - cytology; Respiratory diseases; Reverse Transcriptase Polymerase Chain Reaction; Solubility
• ISSN: 0022-1295; 1540-7748
• DOI: 10.1085/jgp.200709784

Ciliated airway epithelial cells are subject to sustained changes in intracellular CO(2)/HCO(3)(-) during exacerbations of airway diseases, but the role of CO(2)/HCO(3)(-)-sensitive soluble adenylyl cyclase (sAC) in ciliary beat regulation is unknown. We now show not only sAC expression in human airway epithelia (by RT-PCR, Western blotting, and immunofluorescence) but also its specific localization to the axoneme (Western blotting and immunofluorescence). Real time estimations of [cAMP] changes in ciliated cells, using FRET between fluorescently tagged PKA subunits (expressed under the foxj1 promoter solely in ciliated cells), revealed CO(2)/HCO(3)(-)-mediated cAMP production. This cAMP production was specifically blocked by sAC inhibitors but not by transmembrane adenylyl cyclase (tmAC) inhibitors. In addition, this cAMP production stimulated ciliary beat frequency (CBF) independently of intracellular pH because PKA and sAC inhibitors were uniquely able to block CO(2)/HCO(3)(-)-mediated changes in CBF (while tmAC inhibitors had no effect). Thus, sAC is localized to motile airway cilia and it contributes to the regulation of human airway CBF. In addition, CO(2)/HCO(3)(-) increases indeed reversibly stimulate intracellular cAMP production by sAC in intact cells.