Role of Cystic Fibrosis Bronchial Epithelium in Neutrophil Chemotaxis

A hallmark of cystic fibrosis (CF) chronic respiratory disease is an extensive neutrophil infiltrate in the mucosa filling the bronchial lumen, starting early in life for CF infants. The genetic defect of the CF Transmembrane conductance Regulator (CFTR) ion channel promotes dehydration of the airwa...

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Detalles Bibliográficos
Autores principales: Cabrini, Giulio, Rimessi, Alessandro, Borgatti, Monica, Lampronti, Ilaria, Finotti, Alessia, Pinton, Paolo, Gambari, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427443/
https://www.ncbi.nlm.nih.gov/pubmed/32849500
http://dx.doi.org/10.3389/fimmu.2020.01438

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427443/
https://www.ncbi.nlm.nih.gov/pubmed/32849500
http://dx.doi.org/10.3389/fimmu.2020.01438

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