Chahrazed Boulkeroua 1 , Houda Ayari 1 , Taoufik Khalfaoui 1 , Mylène Lafrance 1 , Élie Besserer-Offroy 1 , Nadia Ekindi 2 , Robert Sabbagh 3,4 , Robert Dumaine 1,4 , Olivier Lesur 4,5 , Philippe Sarret 1,4 , Ahmed Chraibi 1,6 . Show Affiliations »
Abstract
BACKGROUND/AIMS: Apelin and its G protein-coupled receptor APJ (gene symbol Aplnr) are strongly expressed in magnocellular vasopressinergic neurons suggesting that the apelin/APJ system plays a key role at the central level in regulating salt and water balance by counteracting the antiduretic action of vasopressin (AVP). Likewise, recent studies revealed that apelin exerts opposite effects to those of vasopressin induced on water reabsorption via a direct action on the kidney collecting duct. However, the underlying mechanisms of the peripheral action of apelin are not clearly understood. Here, we thus investigated the role of the apelin/APJ system in the regulation of water balance in the kidney, and more specifically its involvement in modulating the function of aquaporin-2 (AQP2) in the collecting duct. METHODS: Mouse cortical collecting duct cells (mpkCCD) were incubated in the presence of dDAVP and treated with or without apelin-13. Changes in AQP2 expression and localization were determined by immunoblotting and confocal immunofluorescence staining. RESULTS: Herein, we showed that the APJ was present in mpkCCD cells. Treatment of mpkCCD with apelin-13 reduced the cAMP production and antagonized the AVP-induced increase in AQP2 mRNA and protein expressions. Immunofluorescent experiments also revealed that the AVP-induced apical cell surface expression of AQP2, and notably its phosphorylated isoform AQP2-pS269, was considerably reduced following apelin-13 application to mpkCCD cells. CONCLUSION: Our data reinforce the aquaretic role of the apelin/APJ system in the fine regulation of body fluid homeostasis at the kidney level and its physiological opposite action to the antiduretic activity of AVP. © Copyright by the Author(s). Published by Cell Physiol Biochem Press.
BACKGROUND/AIMS: Apelin and its G protein-coupled receptor APJ (gene symbol Aplnr ) are strongly expressed in magnocellular vasopressinergic neurons suggesting that the apelin /APJ system plays a key role at the central level in regulating salt and water balance by counteracting the antiduretic action of vasopressin (AVP). Likewise, recent studies revealed that apelin exerts opposite effects to those of vasopressin induced on water reabsorption via a direct action on the kidney collecting duct. However, the underlying mechanisms of the peripheral action of apelin are not clearly understood. Here, we thus investigated the role of the apelin /APJ system in the regulation of water balance in the kidney, and more specifically its involvement in modulating the function of aquaporin-2 (AQP2 ) in the collecting duct. METHODS: Mouse cortical collecting duct cells (mpkCCD ) were incubated in the presence of dDAVP and treated with or without apelin -13. Changes in AQP2 expression and localization were determined by immunoblotting and confocal immunofluorescence staining. RESULTS: Herein, we showed that the APJ was present in mpkCCD cells. Treatment of mpkCCD with apelin -13 reduced the cAMP production and antagonized the AVP-induced increase in AQP2 mRNA and protein expressions. Immunofluorescent experiments also revealed that the AVP-induced apical cell surface expression of AQP2 , and notably its phosphorylated isoform AQP2 -pS269, was considerably reduced following apelin -13 application to mpkCCD cells. CONCLUSION: Our data reinforce the aquaretic role of the apelin /APJ system in the fine regulation of body fluid homeostasis at the kidney level and its physiological opposite action to the antiduretic activity of AVP. © Copyright by the Author(s). Published by Cell Physiol Biochem Press.
Entities: CellLine
Chemical
Gene
Species
Keywords:
Apelin; Aquaporin; Confocal microscopy; Kidney; PCR; Vasopressin; mpkCCD
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Substances: See more »
Year: 2019
PMID: 31577078 DOI: 10.33594/000000165
Source DB: PubMed Journal: Cell Physiol Biochem ISSN: 1015-8987