Matches in SemOpenAlex for { <https://semopenalex.org/work/W1946395815> ?p ?o ?g. }
- W1946395815 endingPage "265" @default.
- W1946395815 startingPage "259" @default.
- W1946395815 abstract "The gene product affected in cystic fibrosis, the cystic fibrosis transmembrane conductance regulator (CFTR), is a chlorideselective ion channel that is regulated by cAMP-dependent protein kinase-mediated phosphorylation, ATP binding and ATP hydrolysis. Mutations in the CFTR gene may result in cystic fibrosis characterized by severe pathology (e.g. recurrent pulmonary infection, male infertility and pancreatic insufficiency) involving organs expressing the CFTR. Interestingly, in the kidney, where expression of the CFTR has been reported, impaired ion transport in patients suffering from cystic fibrosis could not be observed. To understand the role of the CFTR in chloride transport in the kidney, we attempted to identify an epithelial cell line that can serve as a model. We demonstrate that the CFTR is expressed constitutively in Madine-Darby canine kidney (MDCK) type I cells, which are thought to have originated from the distal tubule of the dog nephron. We show expression at the mRNA level, using reverse transcriptase-PCR, and at the protein level, using Western blot analysis with three different monoclonal antibodies. Iodide efflux measurements indicate that CFTR expression confers a plasma membrane anion conductance that is responsive to stimulation by cAMP. The cAMP-stimulated iodide release is sensitive to glybenclamide, diphenylamine carboxylic acid and 5-nitro-2-(3-phenylpropylamino)benzoic acid, but not to 4,4'-di-isothiocyanostilbene-2,2'-disulphonic acid, an inhibitor profile characteristic of the CFTR chloride channel. Finally, the polarized localization of the CFTR to the apical plasma membrane was established by iodide efflux measurements and cell-surface biotinylation on MDCK I monolayers. Interestingly, MDCK type II cells, which are thought to have originated from the proximal tubule of the kidney, lack CFTR protein expression and cAMP-stimulated chloride conductance. In conclusion, we propose that MDCK type I and II cells can serve as convenient model systems to study the physiological role and differential expression of CFTR in the distal and proximal tubule respectively." @default.
- W1946395815 created "2016-06-24" @default.
- W1946395815 creator A5024231992 @default.
- W1946395815 creator A5049400835 @default.
- W1946395815 creator A5052136826 @default.
- W1946395815 creator A5062402710 @default.
- W1946395815 creator A5063705444 @default.
- W1946395815 creator A5064028642 @default.
- W1946395815 creator A5066007677 @default.
- W1946395815 creator A5067951639 @default.
- W1946395815 date "1997-02-15" @default.
- W1946395815 modified "2023-09-23" @default.
- W1946395815 title "Functional expression and apical localization of the cystic fibrosis transmembrane conductance regulator in MDCK I cells" @default.
- W1946395815 cites W120703973 @default.
- W1946395815 cites W1556308744 @default.
- W1946395815 cites W1565049236 @default.
- W1946395815 cites W1606812696 @default.
- W1946395815 cites W1638694981 @default.
- W1946395815 cites W165204032 @default.
- W1946395815 cites W1677528798 @default.
- W1946395815 cites W1786021994 @default.
- W1946395815 cites W1878346953 @default.
- W1946395815 cites W1949252567 @default.
- W1946395815 cites W1965857079 @default.
- W1946395815 cites W1969697265 @default.
- W1946395815 cites W1976965004 @default.
- W1946395815 cites W1979867662 @default.
- W1946395815 cites W1987760846 @default.
- W1946395815 cites W1988101098 @default.
- W1946395815 cites W1998130586 @default.
- W1946395815 cites W2005644246 @default.
- W1946395815 cites W2006882142 @default.
- W1946395815 cites W2010309531 @default.
- W1946395815 cites W2010691166 @default.
- W1946395815 cites W2012280093 @default.
- W1946395815 cites W201309019 @default.
- W1946395815 cites W2013454744 @default.
- W1946395815 cites W2014319545 @default.
- W1946395815 cites W2022322532 @default.
- W1946395815 cites W2033969190 @default.
- W1946395815 cites W2039599894 @default.
- W1946395815 cites W2041907482 @default.
- W1946395815 cites W2049914201 @default.
- W1946395815 cites W2052588826 @default.
- W1946395815 cites W2062916647 @default.
- W1946395815 cites W2064811005 @default.
- W1946395815 cites W2078920860 @default.
- W1946395815 cites W2078956864 @default.
- W1946395815 cites W2079234445 @default.
- W1946395815 cites W2081005278 @default.
- W1946395815 cites W2085868009 @default.
- W1946395815 cites W2091585528 @default.
- W1946395815 cites W2096316556 @default.
- W1946395815 cites W2098159540 @default.
- W1946395815 cites W2106799985 @default.
- W1946395815 cites W2124333891 @default.
- W1946395815 cites W2129391213 @default.
- W1946395815 cites W2132452783 @default.
- W1946395815 cites W2133301365 @default.
- W1946395815 cites W2142285863 @default.
- W1946395815 cites W2156523433 @default.
- W1946395815 cites W2162097287 @default.
- W1946395815 cites W2167231609 @default.
- W1946395815 cites W2173634416 @default.
- W1946395815 cites W2399022058 @default.
- W1946395815 cites W2407993662 @default.
- W1946395815 doi "https://doi.org/10.1042/bj3220259" @default.
- W1946395815 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1218186" @default.
- W1946395815 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9078271" @default.
- W1946395815 hasPublicationYear "1997" @default.
- W1946395815 type Work @default.
- W1946395815 sameAs 1946395815 @default.
- W1946395815 citedByCount "61" @default.
- W1946395815 countsByYear W19463958152012 @default.
- W1946395815 countsByYear W19463958152013 @default.
- W1946395815 countsByYear W19463958152016 @default.
- W1946395815 countsByYear W19463958152017 @default.
- W1946395815 countsByYear W19463958152018 @default.
- W1946395815 countsByYear W19463958152021 @default.
- W1946395815 countsByYear W19463958152023 @default.
- W1946395815 crossrefType "journal-article" @default.
- W1946395815 hasAuthorship W1946395815A5024231992 @default.
- W1946395815 hasAuthorship W1946395815A5049400835 @default.
- W1946395815 hasAuthorship W1946395815A5052136826 @default.
- W1946395815 hasAuthorship W1946395815A5062402710 @default.
- W1946395815 hasAuthorship W1946395815A5063705444 @default.
- W1946395815 hasAuthorship W1946395815A5064028642 @default.
- W1946395815 hasAuthorship W1946395815A5066007677 @default.
- W1946395815 hasAuthorship W1946395815A5067951639 @default.
- W1946395815 hasBestOaLocation W19463958152 @default.
- W1946395815 hasConcept C126322002 @default.
- W1946395815 hasConcept C134018914 @default.
- W1946395815 hasConcept C145822097 @default.
- W1946395815 hasConcept C153911025 @default.
- W1946395815 hasConcept C185592680 @default.
- W1946395815 hasConcept C2776938444 @default.
- W1946395815 hasConcept C2778428886 @default.
- W1946395815 hasConcept C3018436504 @default.