Apical membranes of human airway epithelial cells have significant chloride permeability, which is reduced in cystic fibrosis (CF), causing abnormal electrochemistry and impaired mucociliary clearance. At least four types of chloride channels have been identified in these cells, but their relative roles in total permeability and CF are unclear. Noise analysis was used to measure the conductance of chloride channels in human nasal epithelial cells. The data indicate that channels with a mean conductance of 4.5 pS carry most of the chloride current, and that the mean number of such channels per cell is approximately 4,000. Chloride channels in this conductance range were also seen in single-channel recordings
The raised transepithelial electric potential difference (PD) across respiratory epithelia in cystic...
Cystic fibrosis (CF) is a multi-organ autosomal recessive disease of fluid-transporting epithelia, d...
AbstractHuman tracheal gland cells are believed to be a major site at the origin of cystic fibrosis....
The single-channel inside-out patch clamp technique was used to characterize chloride channels in th...
AbstractTransepithelial fluctuation analysis (noise analysis) provides valuable information about th...
1. Employing a primary cell culture system and intracellular microelectrodes, we quantitated and com...
La réduction de la conductance de Cl−de la membrane cellulaire apicale et l'augmentation de la condu...
PurposeCystic fibrosis (CF) is a multisystem genetic disease caused by dysfunction of the epithelial...
The rate of Cl- secretion by human airway epithelium is determined, in part, by apical cell membrane...
AbstractA chloride-selective channel has been found using patch-clamp electrophysiology in human ski...
Cystic fibrosis (CF) is caused by mutations in the Cystic Fibrosis Trans-membrane conductance Regula...
Loss of cystic fibrosis transmembrane conductance regulator (CFTR) anion channel function causes cys...
Calcium-activated Cl- secretion is an important modulator of regulated ion transport in murine airwa...
Calcium-activated Cl(-) secretion is an important modulator of regulated ion transport in murine air...
Background. Cystic fibrosis is characterized by abnormal electrolyte transport across the epithelia ...
The raised transepithelial electric potential difference (PD) across respiratory epithelia in cystic...
Cystic fibrosis (CF) is a multi-organ autosomal recessive disease of fluid-transporting epithelia, d...
AbstractHuman tracheal gland cells are believed to be a major site at the origin of cystic fibrosis....
The single-channel inside-out patch clamp technique was used to characterize chloride channels in th...
AbstractTransepithelial fluctuation analysis (noise analysis) provides valuable information about th...
1. Employing a primary cell culture system and intracellular microelectrodes, we quantitated and com...
La réduction de la conductance de Cl−de la membrane cellulaire apicale et l'augmentation de la condu...
PurposeCystic fibrosis (CF) is a multisystem genetic disease caused by dysfunction of the epithelial...
The rate of Cl- secretion by human airway epithelium is determined, in part, by apical cell membrane...
AbstractA chloride-selective channel has been found using patch-clamp electrophysiology in human ski...
Cystic fibrosis (CF) is caused by mutations in the Cystic Fibrosis Trans-membrane conductance Regula...
Loss of cystic fibrosis transmembrane conductance regulator (CFTR) anion channel function causes cys...
Calcium-activated Cl- secretion is an important modulator of regulated ion transport in murine airwa...
Calcium-activated Cl(-) secretion is an important modulator of regulated ion transport in murine air...
Background. Cystic fibrosis is characterized by abnormal electrolyte transport across the epithelia ...
The raised transepithelial electric potential difference (PD) across respiratory epithelia in cystic...
Cystic fibrosis (CF) is a multi-organ autosomal recessive disease of fluid-transporting epithelia, d...
AbstractHuman tracheal gland cells are believed to be a major site at the origin of cystic fibrosis....