Literature DB >> 1705179

Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance.

N Kartner1, J W Hanrahan, T J Jensen, A L Naismith, S Z Sun, C A Ackerley, E F Reyes, L C Tsui, J M Rommens, C E Bear.   

Abstract

The nature of involvement of the cystic fibrosis gene product (CFTR) in epithelial anion transport is not yet understood. We have expressed CFTR in Sf9 insect cells using the baculovirus expression vector system. Reactivity with antibodies against 12 different epitopes spanning the entire sequence suggested that the complete polypeptide chain was synthesized. Immunogold labeling showed localization to both cell-surface and intracellular membranes. Concomitant with CFTR expression, these cells exhibited a new cAMP-stimulated anion permeability. This conductance, monitored both by radioiodide efflux and patch clamping, strongly resembled that present in several CFTR-expressing human epithelial cells. These findings demonstrate that CFTR can function in heterologous nonepithelial cells and lend support to the possibility that CFTR may itself be a regulated anion channel.

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Year:  1991        PMID: 1705179     DOI: 10.1016/0092-8674(91)90498-n

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  140 in total

1.  A novel CFTR disease-associated mutation causes addition of an extra N-linked oligosaccharide.

Authors:  M M Hämmerle; A A Aleksandrov; X B Chang; J R Riordan
Journal:  Glycoconj J       Date:  2000-11       Impact factor: 2.916

2.  Noise analysis and single-channel observations of 4 pS chloride channels in human airway epithelia.

Authors:  M Duszyk; A S French; S F Man
Journal:  Biophys J       Date:  1992-02       Impact factor: 4.033

3.  Intrinsic anion channel activity of the recombinant first nucleotide binding fold domain of the cystic fibrosis transmembrane regulator protein.

Authors:  N Arispe; E Rojas; J Hartman; E J Sorscher; H B Pollard
Journal:  Proc Natl Acad Sci U S A       Date:  1992-03-01       Impact factor: 11.205

4.  Properties of single- and double-barreled Cl channels of shark rectal gland in planar bilayers.

Authors:  S C Sansom; S L Carosi
Journal:  J Membr Biol       Date:  1992-02       Impact factor: 1.843

5.  The cystic fibrosis transmembrane conductance regulator chloride channel. Iodide block and permeation.

Authors:  J A Tabcharani; X B Chang; J R Riordan; J W Hanrahan
Journal:  Biophys J       Date:  1992-04       Impact factor: 4.033

6.  Small-conductance Cl- channels in rabbit parietal cells activated by prostaglandin E2 and inhibited by GTP gamma S.

Authors:  H Sakai; N Takeguchi
Journal:  J Physiol       Date:  1993-02       Impact factor: 5.182

Review 7.  Outwardly rectifying chloride channels and CF: a divorce and remarriage.

Authors:  W B Guggino
Journal:  J Bioenerg Biomembr       Date:  1993-02       Impact factor: 2.945

8.  A novel mutation in exon 3 of the CFTR gene.

Authors:  H Guillermit; M Jéhanne; I Quéré; M P Audrézet; B Mercier; C Férec
Journal:  Hum Genet       Date:  1993-04       Impact factor: 4.132

9.  Antisense oligodeoxynucleotide to the cystic fibrosis transmembrane conductance regulator inhibits cyclic AMP-activated but not calcium-activated cell volume reduction in a human pancreatic duct cell line.

Authors:  H Kopelman; C Gauthier; M Bornstein
Journal:  J Clin Invest       Date:  1993-03       Impact factor: 14.808

10.  Effects of the delta F508 mutation on the structure, function, and folding of the first nucleotide-binding domain of CFTR.

Authors:  P J Thomas; P L Pedersen
Journal:  J Bioenerg Biomembr       Date:  1993-02       Impact factor: 2.945

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