Journal
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volume 292, Issue 4, Pages C1485-C1492Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00447.2006
Keywords
oxalate; formate; chloride; duodenum
Categories
Funding
- NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK033793, P01DK017433, K08DK067245, R37DK033793] Funding Source: NIH RePORTER
- NIDDK NIH HHS [P01-DK-17433, K08 DK067245, R01-DK-33793, K08-DK-067245, R37 DK033793] Funding Source: Medline
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SLC26A6 ( CFEX, PAT1) is an anion exchanger expressed in several tissues including renal proximal tubule, pancreatic duct, small intestine, liver, stomach, and heart. It has recently been reported that PKC activation inhibits A6- mediated Cl/ HCO3 exchange by disrupting binding of carbonic anhydrase to A6. However, A6 can operate in HCO3-independent exchange modes of physiological importance, as A6- mediated Cl/ oxalate exchange plays important roles in proximal tubule NaCl reabsorption and intestinal oxalate secretion. We therefore examined whether PKC activation affects HCO3-independent exchange modes of Slc26a6 functionally expressed in Xenopus oocytes. We found that PKC activation inhibited Cl/ formate exchange mediated by Slc26a6 but failed to inhibit the related anion exchanger pendrin ( SLC26A4) under identical conditions. PKC activation inhibited Slc26a6-mediated Cl/ formate exchange, Cl/ oxalate exchange, and Cl/ Cl exchange to a similar extent. The inhibitor sensitivity profile and the finding that PMA- induced inhibition was calcium independent suggested a potential role for PKC-delta. Indeed, the PKC-delta-selective inhibitor rottlerin significantly blocked PMA- induced inhibition of Slc26a6 activity. Localization of Slc26a6 by immunofluorescence microscopy demonstrated that exposure to PKC activation led to redistribution of Slc26a6 from the oocyte plasma membrane to the intracellular compartment immediately below it. We also observed that PMA decreased the pool of Slc26a6 available to surface biotinylation but had no effect on total Slc26a6 expression. The physiological significance of these findings was supported by the observation that PKC activation inhibited mouse duodenal oxalate secretion, an effect blocked by rottlerin. We conclude that multiple modes of anion exchange mediated by Slc26a6 are negatively regulated by PKC-delta activation.
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