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

IF 10.3 1区 医学 Q1 UROLOGY & NEPHROLOGY Journal of The American Society of Nephrology Pub Date : 2024-08-26 DOI:10.1681/ASN.0000000000000496
Olivier Devuyst
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Abstract

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 effects on water transport and risk of death and technique failure for patients on dialysis. By 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.

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Aquaporin-1与渗透:腹膜透析中从生理学到精确性。
摘要:水通道的水蒸发素家族的发现为水在生物膜上的移动提供了分子对应物。水通道蛋白在特定细胞类型中的分布、其选择性和极高的水渗透能力以及对其表达和/或贩运的控制是维持多种组织渗透的关键。在此,我们回顾了证明水蒸发素-1(AQP1)促进腹膜内皮细胞水转运的汇聚证据,这是腹膜透析的关键过程--腹膜透析是肾衰竭患者家庭透析治疗的主要方式。在小鼠和细胞模型中进行的遗传学和药理学研究表明,AQP1 在晶体渗透中起着关键作用,对透析患者的水转运、死亡风险和技术衰竭具有临床意义。相比之下,AQP1 在胶体渗透中不起作用。这些研究证实了改善腹膜透析患者自由水转运和超滤的潜在策略。
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来源期刊
Journal of The American Society of Nephrology
Journal of The American Society of Nephrology 医学-泌尿学与肾脏学
CiteScore
22.40
自引率
2.90%
发文量
492
审稿时长
3-8 weeks
期刊介绍: The Journal of the American Society of Nephrology (JASN) stands as the preeminent kidney journal globally, offering an exceptional synthesis of cutting-edge basic research, clinical epidemiology, meta-analysis, and relevant editorial content. Representing a comprehensive resource, JASN encompasses clinical research, editorials distilling key findings, perspectives, and timely reviews. Editorials are skillfully crafted to elucidate the essential insights of the parent article, while JASN actively encourages the submission of Letters to the Editor discussing recently published articles. The reviews featured in JASN are consistently erudite and comprehensive, providing thorough coverage of respective fields. Since its inception in July 1990, JASN has been a monthly publication. JASN publishes original research reports and editorial content across a spectrum of basic and clinical science relevant to the broad discipline of nephrology. Topics covered include renal cell biology, developmental biology of the kidney, genetics of kidney disease, cell and transport physiology, hemodynamics and vascular regulation, mechanisms of blood pressure regulation, renal immunology, kidney pathology, pathophysiology of kidney diseases, nephrolithiasis, clinical nephrology (including dialysis and transplantation), and hypertension. Furthermore, articles addressing healthcare policy and care delivery issues relevant to nephrology are warmly welcomed.
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