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Luminal Na+/H+ exchange in the proximal tubule

Journal

PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
Volume 458, Issue 1, Pages 5-21

Publisher

SPRINGER
DOI: 10.1007/s00424-008-0595-1

Keywords

Acid-based balance; pH regulation; Volume regulation; Sodium transport; Bicarbonate transport; Chloride transport; Sodium-hydrogen exchange; Sodium-proton exchange

Categories

Funding

  1. National Institutes of Health [R01-DK-48482, P01-DK-020543]
  2. Simmons Family Foundation
  3. Charles and Jane Pak Center for Mineral Metabolism and Clinical Research
  4. American Society of Nephrology
  5. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK048482, P01DK020543] Funding Source: NIH RePORTER

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The proximal tubule is critical for whole-organism volume and acid-base homeostasis by reabsorbing filtered water, NaCl, bicarbonate, and citrate, as well as by excreting acid in the form of hydrogen and ammonium ions and producing new bicarbonate in the process. Filtered organic solutes such as amino acids, oligopeptides, and proteins are also retrieved by the proximal tubule. Luminal membrane Na+/H+ exchangers either directly mediate or indirectly contribute to each of these processes. Na+/H+ exchangers are a family of secondary active transporters with diverse tissue and subcellular distributions. Two isoforms, NHE3 and NHE8, are expressed at the luminal membrane of the proximal tubule. NHE3 is the prevalent isoform in adults, is the most extensively studied, and is tightly regulated by a large number of agonists and physiological conditions acting via partially defined molecular mechanisms. Comparatively little is known about NHE8, which is highly expressed at the lumen of the neonatal proximal tubule and is mostly intracellular in adults. This article discusses the physiology of proximal Na+/H+ exchange, the multiple mechanisms of NHE3 regulation, and the reciprocal relationship between NHE3 and NHE8 at the lumen of the proximal tubule.

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