Publication | Open Access
Cloning of the cDNa for a Na+/myo-inositol cotransporter, a hypertonicity stress protein.
341
Citations
20
References
1992
Year
Molecular RegulationMolecular BiologyMechanotransductionCellular PhysiologyTransporter Mrna AccumulationKidney Medullary CellsKidney Tubule RemodelingCell SignalingOsmoregulationCell PhysiologyMechanobiologyMolecular PhysiologyNa+/myo-inositol CotransporterProtein TransportCell BiologyTransporter MrnaProtein PhosphorylationSignal TransductionHypertonicity Stress ProteinNatural SciencesPhysiologyCellular BiochemistryMedicineKidney Research
Kidney medullary cells in situ, as well as kidney-derived Madin-Darby canine kidney (MDCK) cells accumulate nonperturbing, small organic solutes (osmolytes), including myo-inositol, when bathed in hypertonic media. Accumulation of osmolytes balances the osmolality of extracellular fluid without raising intracellular salts that would perturb cellular functions. In hypertonic media, increased myo-inositol accumulation is the result of increased activity of a Na+/myo-inositol cotransporter. We have isolated a cDNA encoding a Na+/myo-inositol cotransporter from MDCK cells using expression in Xenopus oocytes. The cDNA sequence predicts a protein of 718 amino acids with a significant amino acid sequence similarity to the Na+/D-glucose cotransporters of absorbing epithelia. Transporter mRNA is present in kidney and brain and is markedly induced in MDCK cells by medium hypertonicity, demonstrating that adaptation to hypertonic stress involves up-regulation of transporter mRNA accumulation.
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