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J Membr Biol
2004 May 15;1992:85-98. doi: 10.1007/s00232-004-0679-6.
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Control of epithelial ion transport by Cl- and PDZ proteins.
Schreiber R
,
Boucherot A
,
Mürle B
,
Sun J
,
Kunzelmann K
.
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Inhibition of epithelial Na+ channels (ENaC) by the cystic fibrosis transmembrane conductance regulator (CFTR) has been demonstrated previously. Recent studies suggested a role of cytosolic Cl- for the interaction of CFTR with ENaC, when studied in Xenopus oocytes. In the present study we demonstrate that the Na+ / H+ -exchanger regulator factor (NHERF) controls expression of CFTR in mouse collecting duct cells. Inhibition of NHERF largely attenuates CFTR expression, which is paralleled by enhanced Ca(2+) -dependent Cl- secretion and augmented Na+ absorption by the ENaC. It is further demonstrated that epithelial Na+ absorption and ENaC are inhibited by cytosolic Cl- and that stimulation by secretagogues enhances the intracellular Cl- concentration. Thus, the data provide a clue to the question, how epithelial cells can operate as both absorptive and secretory units: Increase in intracellular Cl- during activation of secretion will inhibit ENaC and switch epithelial transport from salt absorption to Cl- secretion.
Boucher,
Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.
1988, Pubmed
Boucher,
Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.
1988,
Pubmed
Boucherot,
Role of CFTR's PDZ1-binding domain, NBF1 and Cl(-) conductance in inhibition of epithelial Na(+) channels in Xenopus oocytes.
2001,
Pubmed
,
Xenbase
Briel,
Cl- transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC.
1998,
Pubmed
,
Xenbase
Chang,
Protein kinase A (PKA) still activates CFTR chloride channel after mutagenesis of all 10 PKA consensus phosphorylation sites.
1993,
Pubmed
Cheng,
A Golgi-associated PDZ domain protein modulates cystic fibrosis transmembrane regulator plasma membrane expression.
2002,
Pubmed
Cuffe,
Basolateral adrenoceptor activation mediates noradrenaline-induced Cl- secretion in M-1 mouse cortical collecting duct cells.
2002,
Pubmed
Cuffe,
ATP stimulates Cl- secretion and reduces amiloride-sensitive Na+ absorption in M-1 mouse cortical collecting duct cells.
2000,
Pubmed
Delpire,
Molecular cloning and chromosome localization of a putative basolateral Na(+)-K(+)-2Cl- cotransporter from mouse inner medullary collecting duct (mIMCD-3) cells.
1994,
Pubmed
Galietta,
Novel CFTR chloride channel activators identified by screening of combinatorial libraries based on flavone and benzoquinolizinium lead compounds.
2001,
Pubmed
Galietta,
Green fluorescent protein-based halide indicators with improved chloride and iodide affinities.
2001,
Pubmed
Grubb,
Anomalies in ion transport in CF mouse tracheal epithelium.
1994,
Pubmed
Hall,
A C-terminal motif found in the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatory factor family of PDZ proteins.
1998,
Pubmed
Jayaraman,
Mechanism and cellular applications of a green fluorescent protein-based halide sensor.
2000,
Pubmed
Jiang,
Epithelial sodium channels regulate cystic fibrosis transmembrane conductance regulator chloride channels in Xenopus oocytes.
2000,
Pubmed
,
Xenbase
Kartner,
Mislocalization of delta F508 CFTR in cystic fibrosis sweat gland.
1992,
Pubmed
Kizer,
Vasopressin and cAMP stimulate electrogenic chloride secretion in an IMCD cell line.
1995,
Pubmed
König,
The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl- concentration.
2001,
Pubmed
,
Xenbase
Konstas,
Cystic fibrosis transmembrane conductance regulator-dependent up-regulation of Kir1.1 (ROMK) renal K+ channels by the epithelial sodium channel.
2002,
Pubmed
,
Xenbase
Korbmacher,
Whole-cell currents in single and confluent M-1 mouse cortical collecting duct cells.
1993,
Pubmed
Köttgen,
N-Acetyl-L-cysteine and its derivatives activate a Cl- conductance in epithelial cells.
1996,
Pubmed
,
Xenbase
Kunzelmann,
ENaC is inhibited by an increase in the intracellular Cl(-) concentration mediated through activation of Cl(-) channels.
2003,
Pubmed
,
Xenbase
Kunzelmann,
Control of epithelial Na+ conductance by the cystic fibrosis transmembrane conductance regulator.
2000,
Pubmed
Kunzelmann,
Mechanisms of the inhibition of epithelial Na(+) channels by CFTR and purinergic stimulation.
2001,
Pubmed
Kunzelmann,
Electrolyte transport in the mammalian colon: mechanisms and implications for disease.
2002,
Pubmed
Kunzelmann,
The cystic fibrosis transmembrane conductance regulator attenuates the endogenous Ca2+ activated Cl- conductance of Xenopus oocytes.
1997,
Pubmed
,
Xenbase
Kunzelmann,
Pharmacotherapy of the ion transport defect in cystic fibrosis: role of purinergic receptor agonists and other potential therapeutics.
2003,
Pubmed
Letz,
Amiloride-sensitive sodium channels in confluent M-1 mouse cortical collecting duct cells.
1995,
Pubmed
,
Xenbase
Letz,
cAMP stimulates CFTR-like Cl- channels and inhibits amiloride-sensitive Na+ channels in mouse CCD cells.
1997,
Pubmed
Mall,
CFTR-mediated inhibition of epithelial Na+ conductance in human colon is defective in cystic fibrosis.
1999,
Pubmed
Mall,
The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.
1998,
Pubmed
Meyer,
Cell swelling activates ATP-dependent voltage-gated chloride channels in M-1 mouse cortical collecting duct cells.
1996,
Pubmed
Moyer,
A PDZ-interacting domain in CFTR is an apical membrane polarization signal.
1999,
Pubmed
Moyer,
The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane.
2000,
Pubmed
Oceandy,
Gene complementation of airway epithelium in the cystic fibrosis mouse is necessary and sufficient to correct the pathogen clearance and inflammatory abnormalities.
2002,
Pubmed
Ogura,
ClC-3B, a novel ClC-3 splicing variant that interacts with EBP50 and facilitates expression of CFTR-regulated ORCC.
2002,
Pubmed
Park,
The cystic fibrosis transmembrane conductance regulator interacts with and regulates the activity of the HCO3- salvage transporter human Na+-HCO3- cotransport isoform 3.
2002,
Pubmed
Raghuram,
A kinase-regulated mechanism controls CFTR channel gating by disrupting bivalent PDZ domain interactions.
2003,
Pubmed
Schreiber,
Effects of purinergic stimulation, CFTR and osmotic stress on amiloride-sensitive Na+ transport in epithelia and Xenopus oocytes.
2003,
Pubmed
,
Xenbase
Schreiber,
Electrolyte transport in the mouse trachea: no evidence for a contribution of luminal K(+) conductance.
2002,
Pubmed
Shen,
Calu-3: a human airway epithelial cell line that shows cAMP-dependent Cl- secretion.
1994,
Pubmed
Short,
An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton.
1998,
Pubmed
Sun,
E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells.
2000,
Pubmed
,
Xenbase
Sun,
Protein kinase A associates with cystic fibrosis transmembrane conductance regulator via an interaction with ezrin.
2000,
Pubmed
Swiatecka-Urban,
PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator.
2002,
Pubmed
Taouil,
Stimulation of beta 2-adrenergic receptor increases cystic fibrosis transmembrane conductance regulator expression in human airway epithelial cells through a cAMP/protein kinase A-independent pathway.
2003,
Pubmed
Wang,
Peptide binding consensus of the NHE-RF-PDZ1 domain matches the C-terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR).
1998,
Pubmed
Wang,
Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity.
2000,
Pubmed
Wei,
The C-terminal part of the R-domain, but not the PDZ binding motif, of CFTR is involved in interaction with Ca(2+)-activated Cl- channels.
2001,
Pubmed