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Surface Hydration Protects Cystic Fibrosis Airways from Infection by Restoring Junctional Networks
Defective hydration of airway surface mucosa is associated with recurrent lung infection in cystic fibrosis (CF), a disease caused by CF transmembrane conductance regulator (CFTR) gene mutations. Whether the composition and/or presence of an airway surface liquid (ASL) is sufficient to prevent infec...
Autores principales: | Simonin, Juliette L., Luscher, Alexandre, Losa, Davide, Badaoui, Mehdi, van Delden, Christian, Köhler, Thilo, Chanson, Marc |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9105190/ https://www.ncbi.nlm.nih.gov/pubmed/35563895 http://dx.doi.org/10.3390/cells11091587 |
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