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Am J Physiol Renal Physiol (July 2, 2002). doi:10.1152/ajprenal.00182.2002
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Articles in PresS, published online ahead of print July 2, 2002
Am J Physiol Renal Physiol, 10.1152/ajprenal.00182.2002
Submitted on May 9, 2002
Accepted on June 27, 2002

Formate-stimulated NaCl absorption in the proximal tubule is independent of the pendrin protein

Lawrence P. Karniski1*, Tong Wang2, Lorraine A. Everett3, Eric D. Green3, Gerhard Giebisch2, and Peter S. Aronson4

1 Department of Internal Medicine, Veterans Affairs Medical Center, Iowa City, Iowa, USA; Department of Internal Medicine, University of Iowa College of Medicine, Iowa City, Iowa, USA
2 Department of Cellular and Molecular Physiology, Yale School of Medicine, New Haven, Connecticut, USA
3 National Human Genome Research Institute, National Institute of Health, Bethesda, Maryland, USA
4 Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut, USA; Department of Cellular and Molecular Physiology, Yale School of Medicine, New Haven, Connecticut, USA

* To whom correspondence should be addressed. E-mail: lawrence-karniski{at}uiowa.edu.

A significant fraction of active chloride reabsorption across the apical membrane of the proximal tubule is mediated by a chloride/formate exchange process, where intracellular formate drives the transport of chloride into the cell. When chloride/formate exchange operates in parallel with Na+/H+ exchange and H+-coupled recycling of formate, the net result is electroneutral NaCl reabsorption. Pendrin is the protein product of the PDS gene (SLC26A4) and functions in several different anion exchange modes including chloride/formate exchange. Pendrin is expressed in the kidney and may serve as the transporter responsible for formate-dependent NaCl reabsorption. In the present study, Pds-knockout mice were used to determine the role of pendrin in proximal tubule chloride reabsorption. We show that formate-dependent NaCl absorption in microperfused proximal tubules is similar between wild-type and pendrin-deficient mice. In addition, there is no difference in the rate of formate-mediated chloride transport in brush border membrane vesicles isolated from wild-type and pendrin-deficient mice. These studies demonstrates that pendrin is not responsible for formate-dependent NaCl reabsorption in the proximal tubule.




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