The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl- concentration


Autoria(s): Konig, J.; Schreiber, R.; Voelcker, T.; Mall, M.; Kunzelmann, K.
Data(s)

01/01/2001

Resumo

Activation of the CFTR Cl- channel inhibits epithelial Na+ channels (ENaC), according to studies on epithelial cells and overexpressing recombinant cells. Here we demonstrate that ENaC is inhibited during stimulation of the cystic fibrosis trans-membrance conductance regulator (CFTR) in Xenopus oocytes, independent of the experimental set-up and the magnitude of the whole-cell current. Inhibition of ENaC is augmented at higher CFTR Cl- currents. Similar to CFTR, ClC-0 Cl- currents also inhibit ENaC, as well as high extracellular Na+ and Cl- in partially permeabilized oocytes. Thus, inhibition of ENaC is not specific to CFTR and seems to be mediated by Cl-.

Identificador

http://espace.library.uq.edu.au/view/UQ:58516

Idioma(s)

eng

Publicador

Oxford Press

Palavras-Chave #Biochemistry & Molecular Biology #Cell Biology #Epithelial Sodium-channels #Xenopus Oocytes #Na+ Conductance #Airway Epithelium #Transport #C1 #270104 Membrane Biology #730110 Respiratory system and diseases (incl. asthma) #0601 Biochemistry and Cell Biology
Tipo

Journal Article