Aquaporin-1 and Osmosis: From Physiology to Precision in Peritoneal Dialysis.


Journal

Journal of the American Society of Nephrology : JASN
ISSN: 1533-3450
Titre abrégé: J Am Soc Nephrol
Pays: United States
ID NLM: 9013836

Informations de publication

Date de publication:
26 Aug 2024
Historique:
received: 06 05 2024
accepted: 20 08 2024
medline: 26 8 2024
pubmed: 26 8 2024
entrez: 26 8 2024
Statut: aheadofprint

Résumé

The discovery of the aquaporin family of water channels has provided a molecular counterpart to the movement of water across biological membranes. The distribution of aquaporins in specific cell types, their selectivity and very high capacity for water permeation, and the control of their expression and/or trafficking are key to sustain osmosis in multiple tissues. Here we review the convergent evidence demonstrating that aquaporin-1 (AQP1) facilitates water transport across endothelial cells in the peritoneal membrane, a key process for peritoneal dialysis - the leading modality of home-based dialysis therapy for patients with kidney failure. Genetic and pharmacologic studies in mouse and cell models indicated that AQP1 plays a critical role in crystalloid osmosis, with clinically relevant impact on water transport and risk of death and technique failure for patients on dialysis. In contrast, AQP1 plays no role in colloid osmosis. These studies substantiate potential strategies to improve free water transport and ultrafiltration in patients treated by peritoneal dialysis.

Identifiants

pubmed: 39186379
doi: 10.1681/ASN.0000000000000496
pii: 00001751-990000000-00402
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : FP7 People: Marie-Curie Actions
ID : 860977
Organisme : European Rare Kidney Disease Reference Network
ID : 739532
Organisme : Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
ID : 310030_189044
Organisme : University of Zurich
ID : URPP ITINERARE

Informations de copyright

Copyright © 2024 by the American Society of Nephrology.

Auteurs

Olivier Devuyst (O)

Mechanisms of Inherited Kidney Disorders, Institute of Physiology, University of Zurich, Zurich, Switzerland; Institut de Recherche Expérimentale et Clinique, UCLouvain, Brussels, Belgium.

Classifications MeSH