Calcium entry is regulated by Zn2+ in relation to extracellular ionic environment in human airway epithelial cells.
Dóra Hargitai, Agnes Pataki, Gábor Raffai, Márta Füzi, Tamás Dankó, László Csernoch, Péter Várnai, Gyula Péter Szigeti, Akos Zsembery
Index: Respir. Physiol. Neurobiol. 170(1) , 67-75, (2010)
Full Text: HTML
Abstract
The extracellular pH, sodium and divalent cation concentrations influence the ATP-induced changes in cytosolic Ca(2+) concentration ([Ca(2+)](i)). This elevation of [Ca(2+)](i) and activation of Ca(2+)-dependent Cl(-) channels represent a possible therapeutic approach in cystic fibrosis (CF). We investigated the changes of [Ca(2+)](i) in different external ionic environment, and P2X purinergic receptors (P2XRs) expression in the control and CF airway epithelial cells. The parallel removal of Na(+) and alkalinization of the extracellular solution increased the amplitude of sustained ATP-induced Ca(2+) signals independent of wild-type or mutant CFTR expression. The ATP-induced Ca(2+) entry was either inhibited or stimulated by Zn(2+) depending on the extracellular Na(+) concentration. In Na(+)-free environment, Zn(2+) and other divalent cations elicited a biphasic Ca(2+) signal. Immunohistochemical data suggest that, multiple subtypes of P2XRs are expressed in these airway epithelial cells. In conclusion, Ca(2+) entry is finely regulated by external ionic environment. Therefore, we speculate that properly compiled aerosols could influence efficacy of zinc-based therapy in CF.Copyright 2009 Elsevier B.V. All rights reserved.
Related Compounds
Related Articles:
ER stress induces epithelial differentiation in the mouse oesophagus.
2015-02-01
[Gut 64(2) , 195-202, (2015)]
2003-08-01
[Neurosci. Res. 46(4) , 463-73, (2003)]
Cellular calcium deficiency plays a role in neuronal death caused by proteasome inhibitors.
2009-06-01
[J. Neurochem. 109(5) , 1225-36, (2009)]
2000-04-01
[Glycobiology 10(4) , 383-91, (2000)]
Amyloid-β peptide-induced secretion of endoplasmic reticulum chaperone glycoprotein GRP94.
2011-01-01
[J. Alzheimers Dis. 27(1) , 61-73, (2011)]