Erratum: Normal CFTR activity and reversed skin potentials in Pseudohypoaldosteronism. (Journal of Membrane Biology (2005) 203, (151-159) DOI: 10.1007/s00232-005-0740-0);Normal CFTR activity and reversed skin potentials in pseudohypoaldosteronism

Journal of Membrane Biology

Volumn 203, Issue 3, 2005, Pages 151-159

  Reddy, M M ^a   Wang, X F ^a   Gottschalk, M ^a   Jones, K ^a   Quinton, P M ^a  

^a UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

Author keywords

CFTR; ENaC; PHA; Sweat eletrolytes

Indexed keywords

ADENOSINE TRIPHOSPHATE; ALPHA TOXIN; AMILORIDE; CHLORIDE CHANNEL; CHLORIDE ION; CYCLIC AMP; PILOCARPINE; SODIUM CHANNEL; SODIUM CHLORIDE; SODIUM ION; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ABSORPTION; ALKALINIZATION; ARTICLE; BASOLATERAL MEMBRANE; CELL FUNCTION; CELL MEMBRANE PERMEABILITY; CELL PH; CONTROLLED STUDY; CYTOSOL; ELECTRIC POTENTIAL; EPITHELIUM CELL; GENE MUTATION; HUMAN; HUMAN TISSUE; PROTEIN PROTEIN INTERACTION; PSEUDOHYPOALDOSTERONISM; SENSITIVITY ANALYSIS; SKIN; SODIUM CONDUCTANCE; SWEAT GLAND; SWEATING;

EID: 21644465164     PISSN: 00222631     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00232-006-1003-4     Document Type: Erratum

References (30)

1. + exchanger isoform 3 in renal polarized epithelial cell model J. Biol. Chem. 277 21480 21488
2. - conductance in secretion by cellular energy levels Am. J. Physiol. 264 C925 C931
3. - impermeability on sweating in cystic fibrosis Am. J. Physiol. 247 C3 C9
4. + channel subunits in normal and cystic fibrosis airways Am. J. Physiol. 269 C511 C518
5. S.S. Chang S. Grander A. Hanukoglu A. Rosler P.M. Mathew I. Hanukoglu L. Schild Y. Lu R.A. Shimkets N.C. Williums B.C. Rossier R.P. Lifton 1996 Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type-1 Nat. Genet. 12 248 253
6. - transport in mutations associated with cystic fibrosis Nature 410 94 97
7. D. Firsov I. Gautschi L. Schild 1998 The heterotetrameric architecture of the epithelial sodium channel (ENaC) EMBO J. 17 344 352
8. D. Firsov R.M. Nicoud S. Gruender L. Schild B.C. Rossier. 1999 Mutational analysis of cystine-rich domains of the epithelium sodium channel (ENaC). Identification of cysteines essential for channel expression at the cell surface J. Biol. Chem. 274 2743 2749
9. - secretion in nasal epithelia of CF mice Am. J. Physiol. 266 C1478 C1483
10. A. Hanukoglu T. Bistritzer Y. Rakover A. Mandelberg 1994 Pseudohypoaldosteronism with increased sweat and saliva electrolyte values and frequent lower respiratory tract infections mimicking cystic fibrosis J. Pediatr. 125 752 755
11. E. Hummler J.D. Horisberger 1999 Genetic disorders of membrane transport. V. The epithelial sodium channel and its implication in human disease Am. J. Physiol. 276 3 G567 G571
12. H.L. Ji M.L. Chalfant B.J. Jovov P. Lockhart S.B. Parker C.M. Fuller B.A. Stanton D.J. Benos 2000 The cytosolic termini of the beta- and gamma-ENaC subunits are involved in the functional interactions between cystic fibrosis transmembrane conductance regulator and epithelial sodium channel J. Biol. Chem. 275 27947 27956
13. E. Kerem T. Bistritzer A. Hanukoglu T. Hofmann Z. Zhou W. Bennett E. MacLaughlin P. Barker M. Nash L. Quittel R. Boucher M.R. Knowles 1999 Pulmonary epithelial sodium channel dysfunction and excess airway liquid in pseudohypoaldosteronism The New Engl. J. Med. 341 156 162
14. D.B. Luckie C.N. Singh J.J. Wine J.H. Wilterding 2001 CFTR activation raises extracellular pH of NIH/3T3 mouse fibroblasts and C127 epithelial cells J. Membrane Biol. 179 275 284
15. J.H. Poulsen H. Fischer B. Illek T.E. Machen 1995 Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator Proc. Natl. Acad. Sci. USA 91 5340 5344
16. P.M. Quinton 1981 Effects of some ion transport inhibitors on reabsorption in intact and perfused single human sweat glands Pfluegers Arch. 391 309 313
17. P.M. Quinton 1983 Chloride impermeability in cystic fibrosis Nature 301 421 422
18. P.M. Quinton 1999 Physiological basis of cystic fibrosis: A historic perspective Physiol. Rev 79 S3 S22
19. P.M. Quinton M.M. Reddy 1992 Control of CFTR Cl conductance by ATP levels through non-hydrolytic binding Nature 360 79 81
20. Reddy, M.M., Light, M.J., Quinton, P.M. Activation of the epithelial Na+ channel (ENaC) requires CFTR Cl- channel function. Nature 402: 301-304
21. M.M. Reddy P.M. Quinton 1999 Intracellular potentials of microperfused human sweat duct cells Pfluegers Arch 410 471 475
22. M.M. Reddy P.M. Quinton 1991 Intracellular potassium activity and the role of potassium in transepithelial salt transport J. Membrane. Biol. 119 199 210
23. - conductance in both cell membranes of an absorptive epithelium J. Membrane. Biol. 130 49 62
24. M.M. Reddy P.M. Quinton 1999 Bumetanide blocks CFTR GC1 in the native sweat duct Am. J. Physiol. 276 C231 C237
25. M.M. Reddy P.M. Quinton 2000 CFTR independent cytosolic basic pH activation of ENaC in the native sweat duct Ped. Pulmonol. 20 Suppl 2000
26. M.M. Reddy P.M. Quinton 2003 Control of dynamic CFTR selectivity by glutamate and ATP in epithelial cells Nature 423 756 759
27. J.A. Schafer 2002 Abnormal regulation of ENaC: syndromes of salt retention and salt wasting by the collecting duct Am. J. Phyiol. 283 F221 F235
28. - transport in a mathematical model of the pancreatic ductal epithelium J. Membrane. Biol. 176 77 100
29. S.S. Strautnieks R.J. Thompson R.M. Gardiner E. Chung 1996 A novel splice site mutation in the gamma subunit of the epithelial sodium channel gene in three type-1 pseudohypoaldosteronism type 1 families Nat. Genet. 13 248 250
30. M.J. Stutts C.M. Canessa J.C. Olsen M. Hamrick J.A. Cohn B.C. Rossier R.C. Boucher 1995 CFTR as a cAMP-dependent regulator of sodium channels Science 269 847 850