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Adhesion-GPCR Gpr116 (ADGRF5) expression inhibits renal acid secretion
Author(s) -
Nathan A. Zaidman,
Viktor Tomilin,
Naghmeh Hassanzadeh Khayyat,
Mahendra Damarla,
Josephine Tidmore,
Diane E. Capen,
Dennis Brown,
Oleh Pochynyuk,
Jennifer L. Pluznick
Publication year - 2020
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.2007620117
Subject(s) - secretion , kidney , endocytosis , microbiology and biotechnology , receptor , chemistry , medicine , endocrinology , renal function , knockout mouse , adhesion , biology , biochemistry , organic chemistry
Significance Gpr116 is an adhesion G protein-coupled receptor (aGPCR) that is highly expressed in the kidney. Here, we report that Gpr116 localizes to A-intercalated cells in the murine collecting duct, where it functions as a significant and critical regulator of renal acid secretion by regulating the surface expression of V-ATPase proton pumps. Kidney-specific Gpr116 knockout mice develop a unique acid-base disorder, “renal tubular alkalosis,” characterized by acidic urine and alkaline blood. These findings have significant implications for other tissues with Gpr116 expression, as well as other acid-secreting epithelia. Furthermore, we propose that Gpr116 may more generally regulate endocytosis, a function that would have wide-ranging implications for both Gpr116 function and for our understanding of aGPCRs.

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