Toll like Receptor signalling by Prevotella histicola activates alternative NF-κB signalling in Cystic Fibrosis bronchial epithelial cells compared to P. aeruginosa

Cystic Fibrosis (CF), caused by mutations affecting the CFTR gene, is characterised by viscid secretions in multiple organ systems. CF airways contain thick mucus, creating a gradient of hypoxia, which promotes the establishment of polymicrobial infection. Such inflammation predisposes to further in...

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Detalles Bibliográficos
Autores principales: Bertelsen, Anne, Elborn, Stuart J., Schock, Bettina C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7544055/
https://www.ncbi.nlm.nih.gov/pubmed/33031374
http://dx.doi.org/10.1371/journal.pone.0235803

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7544055/
https://www.ncbi.nlm.nih.gov/pubmed/33031374
http://dx.doi.org/10.1371/journal.pone.0235803

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