Analysis of nasal potential in murine cystic fibrosis models.

Détails

ID Serval
serval:BIB_A77FBFAC8271
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Analysis of nasal potential in murine cystic fibrosis models.
Périodique
The international journal of biochemistry & cell biology
Auteur⸱e⸱s
da Cunha M.F., Simonin J., Sassi A., Freund R., Hatton A., Cottart C.H., Elganfoud N., Zoubairi R., Dragu C., Jais J.P., Hinzpeter A., Edelman A., Sermet-Gaudelus I.
ISSN
1878-5875 (Electronic)
ISSN-L
1357-2725
Statut éditorial
Publié
Date de publication
11/2016
Peer-reviewed
Oui
Volume
80
Pages
87-97
Langue
anglais
Notes
Publication types: Journal Article ; Review
Publication Status: ppublish
Résumé
The nasal epithelium of the mouse closely mimics the bioelectrical phenotype of the human airways. Ion transport across the nasal epithelium induces a nasal transepithelial potential difference. Its measurement by a relatively non-invasive method adapted from humans allows in vivo longitudinal measurements of CFTR-dependent ionic transport in the murine nasal mucosa. This test offers a useful tool to assess CFTR function in preclinical studies for novel therapeutics modulating CFTR activity. Here we extensively review work done to assess transepithelial transport in the murine respiratory epithelium in the basal state and after administration of CFTR modulators. Factors of variability and discriminative threshold between the CF and the WT mice for different readouts are discussed.
Mots-clé
Animals, Biological Transport, Cystic Fibrosis/genetics, Cystic Fibrosis/metabolism, Cystic Fibrosis/pathology, Cystic Fibrosis/therapy, Disease Models, Animal, Epithelium/metabolism, Epithelium/pathology, Humans, Nasal Mucosa/metabolism, Nose/pathology, CFTR correctors, Cystic fibrosis, Ionic transepithelial transport, Mouse, Nasal potential difference
Pubmed
Web of science
Création de la notice
03/07/2023 16:06
Dernière modification de la notice
04/07/2023 5:55
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