Type II Na-Pi cotransport is regulated transcriptionally by ambient bicarbonate/carbon dioxide tension in OK cells

Author:

Jehle Andreas W.1,Hilfiker Helene1,Pfister Markus F.1,Biber Jürg1,Lederer Eleanor2,Krapf Reto3,Murer Heini1

Affiliation:

1. Institute of Physiology, University of Zurich-Irchel, CH-8057 Zurich, Switzerland;

2. Department of Medicine, Division of Nephrology, University of Louisville, Louisville, Kentucky 40292; and

3. Klinik B für Innere Medizin, Kantonsspital, CH-9007 St. Gallen, Switzerland

Abstract

The purpose of the present study was to determine whether isohydric changes in HCO3 concentration and Pco 2directly affect apical Na-dependent Pi(Na-Pi) cotransport in OK cells (opossum kidney cell line). Cells were kept at either 44 mM NaHCO3/10% CO2, pH 7.4 (high-HCO3/CO2condition), or 22 mM NaHCO3/5% CO2, pH 7.4 (low-HCO3/CO2condition) (for 14–24 h). Incubation in lower HCO3/CO2concentrations increased Na-Picotransport 1.5-fold. The increased Na-Pi cotransport was paralleled by a two- to threefold increased expression of the NaPi-4 transporter protein and a two- to threefold increase in NaPi-4 mRNA abundance. The increase in NaPi-4 mRNA could be completely prevented by incubation in the presence of a transcriptional inhibitor, suggesting that the increase in NaPi-4 mRNA results from an increased NaPi-4 mRNA transcription. In agreement, the NaPi-4 promoter activity was stimulated by 50% at lower HCO3/CO2concentrations. In conclusion, our data demonstrate that isohydric changes in HCO3 concentration and Pco 2exert a significant, direct cellular effect on Na-Pi cotransport and NaPi-4 protein expression in OK cells by affecting NaPi-4 mRNA transcription.

Publisher

American Physiological Society

Subject

Physiology

Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Proximal Tubule Function and Response to Acidosis;Clinical Journal of the American Society of Nephrology;2013-08-01

2. Elevated Carbon Dioxide Blunts Mammalian cAMP Signaling Dependent on Inositol 1,4,5-Triphosphate Receptor-mediated Ca2+ Release;Journal of Biological Chemistry;2012-07

3. Genetic Defects in Renal Phosphate Handling;Genetic Diseases of the Kidney;2009

4. Novel regulatory function for NHERF-1 in Npt2a transcription;American Journal of Physiology-Renal Physiology;2008-04

5. Na+/H+ Exchangers in Renal Regulation of Acid-Base Balance;Seminars in Nephrology;2006-09

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