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The Na+-dependent chloride-bicarbonate exchanger SLC4A8 mediates an electroneutral Na+ reabsorption process in the renal cortical collecting ducts of mice
Françoise Leviel, … , Régine Chambrey, Dominique Eladari
Françoise Leviel, … , Régine Chambrey, Dominique Eladari
Published April 12, 2010
Citation Information: J Clin Invest. 2010;120(5):1627-1635. https://doi.org/10.1172/JCI40145.
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Research Article

The Na+-dependent chloride-bicarbonate exchanger SLC4A8 mediates an electroneutral Na+ reabsorption process in the renal cortical collecting ducts of mice

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Abstract

Regulation of sodium balance is a critical factor in the maintenance of euvolemia, and dysregulation of renal sodium excretion results in disorders of altered intravascular volume, such as hypertension. The amiloride-sensitive epithelial sodium channel (ENaC) is thought to be the only mechanism for sodium transport in the cortical collecting duct (CCD) of the kidney. However, it has been found that much of the sodium absorption in the CCD is actually amiloride insensitive and sensitive to thiazide diuretics, which also block the Na-Cl cotransporter (NCC) located in the distal convoluted tubule. In this study, we have demonstrated the presence of electroneutral, amiloride-resistant, thiazide-sensitive, transepithelial NaCl absorption in mouse CCDs, which persists even with genetic disruption of ENaC. Furthermore, hydrochlorothiazide (HCTZ) increased excretion of Na+ and Cl– in mice devoid of the thiazide target NCC, suggesting that an additional mechanism might account for this effect. Studies on isolated CCDs suggested that the parallel action of the Na+-driven Cl–/HCO3– exchanger (NDCBE/SLC4A8) and the Na+-independent Cl–/HCO3– exchanger (pendrin/SLC26A4) accounted for the electroneutral thiazide-sensitive sodium transport. Furthermore, genetic ablation of SLC4A8 abolished thiazide-sensitive NaCl transport in the CCD. These studies establish what we believe to be a novel role for NDCBE in mediating substantial Na+ reabsorption in the CCD and suggest a role for this transporter in the regulation of fluid homeostasis in mice.

Authors

Françoise Leviel, Christian A. Hübner, Pascal Houillier, Luciana Morla, Soumaya El Moghrabi, Gaëlle Brideau, Hassan Hatim, Mark D. Parker, Ingo Kurth, Alexandra Kougioumtzes, Anne Sinning, Vladimir Pech, Kent A. Riemondy, R. Lance Miller, Edith Hummler, Gary E. Shull, Peter S. Aronson, Alain Doucet, Susan M. Wall, Régine Chambrey, Dominique Eladari

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Figure 1

Pharmacological characterization of transepithelial transport of Na+, K+, and Cl– in collecting ducts isolated from wild-type mice.

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Pharmacological characterization of transepithelial transport of Na+, K+...
(A) Effects of amiloride (10–5 M) and HCTZ (10–4 M) on Na+, Cl–, and K+ transepithelial fluxes and on transepithelial voltage in CCDs isolated from Na+-restricted mice. JNa, rate of Na+ absorption; JCl, rate of Cl– absorption; Vte, transepithelial voltage; JK, rate of K+ secretion. Statistical significance was assessed by ANOVA; comparisons between groups were tested by Bonferroni’s post-hoc test. n = 5 in each group, *P < 0.05 versus control, #P < 0.05 versus low Na+; †P < 0.05 versus low Na+ amiloride (amil). (B) Effects of HCTZ alone (10–4 M) on Na+, Cl–, and K+ transepithelial fluxes and on transepithelial voltage in CCDs isolated from Na+-restricted mice. Statistical significance was assessed by 2-tailed unpaired Student’s t test. n = 5 in each group; *P < 0.05 versus control (low Na).

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