Publication | Closed Access
Thyroid hormone stimulates Na-K-ATPase activity and its plasma membrane insertion in rat alveolar epithelial cells
70
Citations
40
References
2003
Year
Renal InflammationParathyroid GlandCellular PhysiologyAec Cell LinesParathyroid HormoneCell SignalingPlasma Membrane InsertionMolecular PhysiologyBiochemistrySodium HomeostasisCell LinesIon ChannelsMembrane BiologyRenal PathophysiologyNa-k-atpase ActivityEndocrinologyCell BiologyPotassium HomeostasisProtein PhosphorylationSignal TransductionNatural SciencesPhysiologyThyroid HormoneCellular BiochemistryMedicine
Na-K-ATPase protein is critical for maintaining cellular ion gradients and volume and for transepithelial ion transport in kidney and lung. Thyroid hormone, 3,3′,5-triiodo-l-thyronine (T 3 ), given for 2 days to adult rats, increases alveolar fluid resorption by 65%, but the mechanism is undefined. We tested the hypothesis that T 3 stimulates Na-K-ATPase in adult rat alveolar epithelial cells (AEC), including primary rat alveolar type II (ATII) cells, and determined mechanisms of the T 3 effect on the Na-KATPase enzyme using two adult rat AEC cell lines (MP48 and RLE-6TN). T 3 at 10 - 8 and 10 - 5 M increased significantly hydrolytic activity of Na-K-ATPase in primary ATII cells and both AEC cell lines. The increased activity was dose dependent in the cell lines (10 - 9 -10 - 4 M) and was detected within 30 min and peaked at 6 h. Maximal increases in Na-K-ATPase activity were twofold in MP48 and RLE-6TN cells at pharmacological T 3 of 10 - 5 and 10 - 4 M, respectively, but increases were statistically significant at physiological T 3 as low as 10 - 9 M. This effect was T 3 specific, because reverse T 3 (3,3′,5′-triiodo-l-thyronine) at 10 - 9 -10 - 4 M had no effect. The T 3 -induced increase in Na-K-ATPase hydrolytic activity was not blocked by actinomycin D. No significant change in mRNA and total cell protein levels of Na-K-ATPase were detected with 10 - 9 -10 - 5 M T 3 at 6 h. However, T 3 increased cell surface expression of Na-K-ATPase α 1 - or β 1 -subunit proteins by 1.7- and 2-fold, respectively, and increases in Na-K-ATPase activity and cell surface expression were abolished by brefeldin A. These data indicate that T 3 specifically stimulates Na-K-ATPase activity in adult rat AEC. The upregulation involves translocation of Na-K-ATPase to plasma membrane, not increased gene transcription. These results suggest a novel nontranscriptional mechanism for regulation of Na-K-ATPase by thyroid hormone.
| Year | Citations | |
|---|---|---|
Page 1
Page 1