Mechanisms of the inhibition of epithelial Na+ channels by CFTR and purinergic stimulation

Kidney International

Volumn 60, Issue 2, 2001, Pages 455-461

  Kunzelmann, K ^a   Schreiber, R ^a   Boucherot, A ^a  

^a UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

ATP; Cystic fibrosis; ENaC; Purinergic stimulation; Transport proteins; UTP

Indexed keywords

ADENOSINE TRIPHOSPHATE; CHLORIDE; CYCLIC AMP; PURINE RECEPTOR; SODIUM CHANNEL; TRANSMEMBRANE CONDUCTANCE REGULATOR; URIDINE TRIPHOSPHATE;

ANIMAL CELL; CHLORIDE CONDUCTANCE; CONFERENCE PAPER; EPITHELIUM CELL; GENE EXPRESSION; INHIBITION KINETICS; INTESTINE EPITHELIUM; KIDNEY CELL; MEMBRANE CONDUCTANCE; NONHUMAN; PRIORITY JOURNAL; REGULATORY MECHANISM; TRACHEA MUCOSA;

EID: 0034919237     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1755.2001.060002455.x     Document Type: Conference Paper

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3. + conductance is reduced by CFTR in normal but not in CF airways
4. + channels in mouse CCD cells
5. + permeability in cystic fibrosis human primary cell cultures
6. + channel
7. An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton
8. E3KARP mediates the association of Ezrin and PKA with CFTR in airway cells
9. Protein kinase A associates with cystic fibrosis transmembrane conductance regulator via an interaction with ezrin
10. The PDZ interacting domain of CFTR is required for functional expression in the apical plasma membrane
11. Yes-associated protein 65 localizes p62(c-Yes) to the apical compartment of airway epithelia by association with EBP50
12. + absorption in distal bronchi
13. + absorption by extracellular nucleotides in human normal and CF airways
14. + absorption in wildtype and DeltaF508 CFTR-expressing human bronchial epithelia
15. + channels in Xenopus ooyctes coexpressing CFTR and ENaC
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17. Electrolyte transport in the colon: Mechanisms and implications for disease
18. + absorption in M-1 mouse cortical collecting duct cells
19. Extracellular ATP increases [CA(2+)](i) in distal tubule cells. I. Evidence for a P2Y2 purinoceptor
20. The luminal P2Y receptor in the isolated perfused mouse cortical collecting duct
21. Axial distribution and characterization of basolateral P2Y receptors along the rat renal tubule
22. Immunocytochemical localization of the cystic fibrosis gene product CFTR
23. Both the wild type and a functional isoform of CFTR are expressed in kidney
24. Molecular cloning and expression of a cyclic AMP-activated chloride conductance regulator: A novel ATP-binding cassette transporter
25. - channels in principal cells via a cyclic adenosine monophosphate-dependent pathway
26. Ion conductances of isolated cortical collecting duct cells
27. Impaired diluting segment chloride reabsorption in patients with cystic fibrosis
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29. Effect on renal function of essential fatty acid supplementation in cystic fibrosis
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32. + channel via Go guanine nucleotide-binding regulatory protein