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Am J Physiol Renal Physiol 297: F604-F611, 2009. First published July 8, 2009; doi:10.1152/ajprenal.00043.2009
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Downregulation of claudin-2 expression in renal epithelial cells by metabolic acidosis

Daniel F. Balkovetz,1,2,3 Phillip Chumley,1 and Hassane Amlal4

Departments of 1Medicine and 2Cell Biology, University of Alabama at Birmingham, and 3Birmingham Veterans Affairs Medical Center, Birmingham, Alabama; and 4Department of Medicine, College of Medicine, University of Cincinnati, Cincinnati, Ohio

Submitted 26 January 2009 ; accepted in final form 7 July 2009

Chronic metabolic acidosis (CMA) is associated with an inhibition of fluid reabsorption in the renal proximal tubule. The effects of CMA on paracellular transport across the renal epithelial tight junction (TJ) is unknown. Claudin-2 is a transmembrane TJ-associated protein which confers TJ paracellular permeability to Na+. We examined the effects of CMA on the expression of TJ transport proteins using both in vivo and in vitro models of CMA. The results showed downregulation of claudin-2 mRNA and protein expression in the cortex of rats subjected to the NH4Cl loading model of CMA. Madin-Darby canine kidney (MDCK) and HK-2 cells are models of renal epithelial cells and express claudin-2 protein in their TJ. We examined the effects of acidic pH exposure on the expression of claudin-2 in MDCK and HK-2 renal epithelial cells. Exposure of MDCK cells to pH 6.96 medium caused a significant and reversible decrease in claudin-2 protein abundance. A dose-response analysis of acidic medium exposure of MDCK and HK-2 cells demonstrated a downregulation of claudin-2 protein. The downregulation effect of acidic pH is specific to claudin-2 expression as the expression of other TJ-associated proteins (i.e., claudin-1, -3, -4, and -7, occludin, and zonula occludens-1) remained unchanged compared with control pH (7.40). Collectively, these data demonstrate that CMA downregulates the expression of claudin-2 likely through a direct effect of acidic pH. Potential physiological significance of these changes is discussed.

paracellular transport



Address for reprint requests and other correspondence: D. F. Balkovetz, Dept. of Medicine, 1530 3rd. Ave. South, LHRB 642, Univ. of Alabama at Birmingham, Birmingham, AL 35294-0007 (e-mail: balkovet{at}uab.edu)







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