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Quantitative phase imaging to study transmembrane water fluxes regulated by CFTR and AQP3 in living human airway epithelial CFBE cells and CHO cells

In epithelial cells, the cystic fibrosis transmembrane conductance regulator (CFTR), a cAMP-regulated Cl(-) channel, plays a key role in water and electrolytes secretion. A dysfunctional CFTR leads to the dehydration of the external environment of the cells and to the production of viscous mucus in...

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Detalles Bibliográficos
Autores principales: Llinares, Jodie, Cantereau, Anne, Froux, Lionel, Becq, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259668/
https://www.ncbi.nlm.nih.gov/pubmed/32469934
http://dx.doi.org/10.1371/journal.pone.0233439

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