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Dexamethasone and cyclic AMP regulate sodium phosphate cotransporter (NaPi-IIb and Pit-1) mRNA and phosphate uptake in rat alveolar type II epithelial cells

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dc.contributor.author Jin, C en
dc.contributor.author Zoidis, E en
dc.contributor.author Ghirlanda, C en
dc.contributor.author Schmid, C en
dc.date.accessioned 2014-06-06T06:50:11Z
dc.date.available 2014-06-06T06:50:11Z
dc.date.issued 2010 en
dc.identifier.issn 03412040 en
dc.identifier.uri http://dx.doi.org/10.1007/s00408-009-9183-1 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/4992
dc.subject AT II cells en
dc.subject Cyclic AMP en
dc.subject Dexamethasone en
dc.subject Phosphate transporter Pit-1-NaPi-IIb mRNA en
dc.subject Sodium-dependent phosphate transport en
dc.subject.other bucladesine en
dc.subject.other dexamethasone en
dc.subject.other messenger RNA en
dc.subject.other phosphate en
dc.subject.other sodium phosphate cotransporter en
dc.subject.other transcription factor Pit 1 en
dc.subject.other animal cell en
dc.subject.other animal experiment en
dc.subject.other animal tissue en
dc.subject.other article en
dc.subject.other cell isolation en
dc.subject.other cell type en
dc.subject.other controlled study en
dc.subject.other drug effect en
dc.subject.other gene control en
dc.subject.other lung alveolus cell type 2 en
dc.subject.other lung alveolus epithelium en
dc.subject.other male en
dc.subject.other nonhuman en
dc.subject.other Northern blotting en
dc.subject.other nucleotide sequence en
dc.subject.other phosphate transport en
dc.subject.other priority journal en
dc.subject.other protein analysis en
dc.subject.other protein expression en
dc.subject.other protein function en
dc.subject.other protein synthesis en
dc.subject.other protein synthesis regulation en
dc.subject.other rat en
dc.subject.other Western blotting en
dc.subject.other Animals en
dc.subject.other Biological Transport en
dc.subject.other Blotting, Northern en
dc.subject.other Blotting, Western en
dc.subject.other Cell Membrane en
dc.subject.other Cells, Cultured en
dc.subject.other Choline en
dc.subject.other Cyclic AMP en
dc.subject.other Dexamethasone en
dc.subject.other Epithelial Cells en
dc.subject.other Kinetics en
dc.subject.other Male en
dc.subject.other Phenotype en
dc.subject.other Phosphates en
dc.subject.other Pulmonary Alveoli en
dc.subject.other Rats en
dc.subject.other Rats, Wistar en
dc.subject.other RNA, Messenger en
dc.subject.other Sodium en
dc.subject.other Sodium-Phosphate Cotransporter Proteins, Type IIb en
dc.subject.other Sodium-Phosphate Cotransporter Proteins, Type III en
dc.title Dexamethasone and cyclic AMP regulate sodium phosphate cotransporter (NaPi-IIb and Pit-1) mRNA and phosphate uptake in rat alveolar type II epithelial cells en
heal.type journalArticle en
heal.identifier.primary 10.1007/s00408-009-9183-1 en
heal.publicationDate 2010 en
heal.abstract Alveolar epithelial type II (AT II) cells need phosphate (Pi) for surfactant synthesis. The Na-dependent (Nad) Pi transporters NaPi-IIb and Pit-1 are expressed in lung, but their expression, regulation, and function in AT II cells remain unclear. We studied NaPi-IIb and Pit-1 mRNA expression in cultured AT II cells isolated from adult rat lung, their regulation by agents known to enhance surfactant production, dexamethasone (dex) and dibutyryl cyclic AMP (cAMP), and the effects of dex and cAMP on Nad Pi uptake by this cell type. By Northern analysis, cultured AT II cells expressed both NaPi-IIb (4.8 and 4.0 kb) and Pit-1 (4.3 kb) mRNA. Treatment with 100 nmol/l dex for 24 h decreased the expression of both mRNAs (to 0.48 ± 0.06 and 0.77 ± 0.05, respectively, as compared to control), while 0.1 mmol/l cAMP stimulated NaPi-IIb (1.94 ± 0.22) but not Pit-1 mRNA (0.90 ± 0.05, compared to vehicle-treated cells). NaPi-IIb and Pit-1 proteins could not be identified by western analysis of plasma membrane preparations of cultured AT II cells. AT II cells take up Pi in a Nad manner. Uptake was slightly (to 0.78-fold of the control) decreased by 100 nmol/l dex but not affected by 0.1 mmol/l cAMP treatment. Although NaPi-IIb mRNA expression was maintained to some extent by AT II cells kept in primary culture, Pi uptake was more closely related to Pit-1 mRNA expression. © 2009 Springer Science+Business Media, LLC. en
heal.journalName Lung en
dc.identifier.issue 1 en
dc.identifier.volume 188 en
dc.identifier.doi 10.1007/s00408-009-9183-1 en
dc.identifier.spage 51 en
dc.identifier.epage 61 en


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