RT Journal Article SR Electronic T1 Apical dehydration impairs the cystic fibrosis airway epithelium barrier via a β1-integrin/YAP1 pathway JF Life Science Alliance JO Life Sci. Alliance FD Life Science Alliance LLC SP e202302449 DO 10.26508/lsa.202302449 VO 7 IS 4 A1 Simonin, Juliette L A1 Tomba, Caterina A1 Mercier, Vincent A1 Bacchetta, Marc A1 Idris, Tahir A1 Badaoui, Mehdi A1 Roux, Aurélien A1 Chanson, Marc YR 2024 UL https://www.life-science-alliance.org/content/7/4/e202302449.abstract AB Defective hydration of airway surface mucosa is associated with lung infection in cystic fibrosis (CF), partly caused by disruption of the epithelial barrier integrity. Although rehydration of the CF airway surface liquid (ASL) alleviates epithelium vulnerability to infection by junctional protein expression, the mechanisms linking ASL to barrier integrity are unknown. We show here the strong degradation of YAP1 and TAZ proteins in well-polarized CF human airway epithelial cells (HAECs), a process that was prevented by ASL rehydration. Conditional silencing of YAP1 in rehydrated CF HAECs indicated that YAP1 expression was necessary for the maintenance of junctional complexes. A higher plasma membrane tension in CF HAECs reduced endocytosis, concurrent with the maintenance of active β1-integrin ectopically located at the apical membrane. Pharmacological inhibition of β1-integrin accumulation restored YAP1 expression in CF HAECs. These results indicate that dehydration of the CF ASL affects epithelial plasma membrane tension, resulting in ectopic activation of a β1-integrin/YAP1 signaling pathway associated with degradation of junctional proteins.