Modulation of Ca2|[plus]|-Activated Cl|[minus]| Secretion by Basolateral K|[plus]| Channels in Human Normal and Cystic Fibrosis Airway Epithelia

摘要

Human airway epithelia express Ca2+-activated Cl? channels (CaCC) that are activated by extracellular nucleotides (ATP and UTP). CaCC is preserved and seems to be up-regulated in the airways of cystic fibrosis (CF) patients. In the present study, we examined the role of basolateral K+ channels in CaCC-mediated Cl? secretion in native nasal tissues from normal individuals and CF patients by measuring ion transport in perfused micro Ussing chambers. In the presence of amiloride, UTP-mediated peak secretory responses were increased in CF compared with normal nasal tissues. Activation of the cAMP pathway further increased CaCC-mediated secretion in CF but not in normal nasal mucosa. CaCC-dependent ion transport was inhibited by the chromanol 293B, an inhibitor of cAMP-activated hKvLQT1 K+ channels, and by clotrimazole, an inhibitor of Ca2+-activated hSK4 K+ channels. The K+ channel opener 1-ethyl-2-benzimidazolinone further increased CaCC-mediated Cl? secretion in normal and CF tissues. Expression of hSK4 as well as hCACC-2 and hCACC-3 but not hCACC-1 was demonstrated by reverse transcriptase PCR on native nasal tissues. We conclude that Ca2+-activated Cl? secretion in native human airway epithelia requires activation of Ca2+-dependent basolateral K+ channels (hSK4). Co-activation of hKvLQT1 improves CaCC-mediated Cl? secretion in native CF airway epithelia, and may have a therapeutic effect in the treatment of CF lung disease.Abbreviations: CaCC, Ca2+-activated Cl? channel; CF, cystic fibrosis; CFTR, cystic fibrosis transmembrane conductance regulator; 1-EBIO, 1-ethyl-2-benzimidazolinone; Isc, equivalent short circuit current; Rte, transepithelial resistance; UTP, uridine5′-triphosphate; Vte, transepithelial voltage