UTP inhibits Na+ absorption in wild-type and Delta F508 CFTR-expressing human bronchial epithelia

Ca2+-mediated agonists, including UTP, are being developed for therapeutic use in cystic fibrosis (CF) based on their ability to modulate alternative Cl- conductances. As CF is also characterized by hyperabsorption of Na+, we determined the effect of mucosal UTP on transepithelial Na+ transport in p rimary cultures of human bronchial epithelia (HBE). In symmetrical NaCl, UT P induced an initial increase in short-circuit current (I-sc) followed by a sustained inhibition. To differentiate between effects on Na+ absorption a nd Cl- secretion, I-sc was measured in the absence of mucosal and serosal C l- (I-Na) Again, mucosal UTP induced an initial increase and then a sustain ed decrease that reduced amiloride-sensitive I-Na by 73%. The Ca2+-dependen t agonists histamine, bradykinin, serosal UTP, and thapsigargin similarly i nduced sustained inhibition (62-84%) of I-Na Mucosal UTP induced similar su stained inhibition (half-maximal inhibitory concentration 296 nM) of I-Na i n primary cultures of human CF airway homozygous for the Delta F508 mutatio n. BAPTA-AM. blunted UTP-dependent inhibition of I-Na, but inhibitors of pr otein kinase C (PKC) and phospholipase A(2) had no effect. Indeed, direct a ctivation of PKC by phorbol 12-myristate 13-acetate failed to inhibit Na+ a bsorption. Apyrase, a tri- and diphosphatase, did not reverse inhibitory ef fects of UTP on I-Na, suggesting a long-term inhibitory effect of UTP that is independent of receptor occupancy. After establishment of a mucosa-to-se rosa K+ concentration gradient and permeabilization of the mucosal membrane with nystatin, mucosal UTP induced an initial increase in K+ current follo wed by a sustained inhibition. We conclude that increasing cellular Ca2+ in duces a long-term inhibition of transepithelial Na+ transport across normal and CF HBE at least partly due to downregulation of a basolateral membrane K+ conductance. Thus UTP may have a dual therapeutic effect in CF airway: 1) simulation of a Cl- secretory response and 2) inhibition of Na+ transpor t.