WNK Inhibition Increases Surface Liquid pH and Host Defense in Cystic Fibrosis Airway Epithelia

In cystic fibrosis (CF), reduced HCO₃² secretion acidifies the airway surface liquid (ASL), and the acidic pH disrupts host defenses. Thus, understanding the control of ASL pH (pH_ASL) in CF may help identify novel targets and facilitate therapeutic development. In diverse epithelia, the WNK (with-no-lysine [K]) kinases coordinate HCO₃² and Cl² transport, but their functions in airway epithelia are poorly understood. Here, we tested the hypothesis that WNK kinases regulate CF pH_ASL. In primary cultures of differentiated human airway epithelia, inhibiting WNK kinases acutely increased both CF and non-CF pH_ASL. This response was HCO₃² dependent and involved downstream SPAK/OSR1 (Ste20/SPS1-related prolinealanine-rich protein kinase/oxidative stress responsive 1 kinase). Importantly, WNK inhibition enhanced key host defenses otherwise impaired in CF. Human airway epithelia expressed two WNK isoforms in secretory cells and ionocytes, and knockdown of either WNK1 or WNK2 increased CF pH_ASL. WNK inhibition decreased Cl² secretion and the response to bumetanide, an NKCC1 (sodium-potassium-chloride cotransporter 1) inhibitor. Surprisingly, bumetanide alone or basolateral Cl² substitution also alkalinized CF pH_ASL. These data suggest that WNK kinases influence the balance between transepithelial Cl² versus HCO₃² secretion. Moreover, reducing basolateral Cl² entry may increase HCO₃² secretion and raise pH_ASL, thereby improving CF host defenses.