Faculty, Staff and Student Publications

Language

English

Publication Date

10-28-2025

Journal

Function

DOI

10.1093/function/zqaf048

PMID

41091845

PMCID

PMC12586993

PubMedCentral® Posted Date

10-14-2025

PubMedCentral® Full Text Version

Post-print

Abstract

Kidneys are central in maintaining acid-base homeostasis by recovering filtered bicarbonate (HCO3-) in the proximal tubule and by secreting H+ in the collecting duct. Here, we demonstrate a critical role of the exchange protein directly activated by cAMP (Epac) signaling, and particularly the Epac2, in governing renal adaptation to dietary acid load. RNAseq analysis of the renal cortical area revealed that Epac1&2 deficiency was associated with changes in gene profile seen in acidosis. Renal expression of Epac2 but not Epac1 was enhanced by acid load. Epac2-/- mice developed a pronounced metabolic acidosis due to the inability to acidify urine in response to dietary acid load. Deletion of Epac2 and Epac1 exerted additive inhibitory actions on expression of the Na+/H+ exchanger (NHE-3, Slc9a3) in the proximal tubule. Using super-resolution STED microscopy, we detected NHE-3 redistribution to the base of the brush border, which led to the impaired recovery after acidification in freshly isolated split-opened proximal tubules from Epac1&2-/- mice. Deletion of Epac2 but not Epac1 diminished H+ secretion in freshly isolated split-opened collecting ducts, compromised apical translocation of V-ATPase, and reduced anion exchanger 1 (AE1, Slc4a1) expression in the A-type intercalated cells, and caused lower levels of titratable acids in urine, whereas ammoniagenesis was not compromised. Overall, we demonstrate a previously unrecognized role of Epac signaling in renal adaptation to dietary acidification. While both Epac1 and Epac2 isoforms control NHE-3-dependent H+ secretion in the proximal tubule, only Epac2 is essential to augment H+ transport in the collecting duct to acidify urine.

Keywords

Animals, Guanine Nucleotide Exchange Factors, Mice, Mice, Knockout, Nephrons, Sodium-Hydrogen Exchanger 3, Adaptation, Physiological, Hydrogen-Ion Concentration, Sodium-Hydrogen Exchangers, Male, Kidney Tubules, Proximal, Acidosis, metabolic acidosis, NHE-3, AE1, proximal tubule, collecting duct, intercalated cells

Published Open-Access

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