Aquaporin-2 Water Channel Mutations Causing Nephrogenic Diabetes Insipidus

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Title: Aquaporin-2 Water Channel Mutations Causing Nephrogenic Diabetes Insipidus
Authors: van Os, Carel; Deen, Peter M.T.
Publisher: Proceedings of the Association of American Physicians
Date Published: September 1998 - October 1998
Reference Number: 398
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Since the discovery of aquaporin water channels, insight into the molecular mechanism by which rapid osmotic water occurs across cell membranes has greatly improved. Aquaporin-2 is the vasopressin-responsive water channel in the collecting duct, and vasopressin control of water permeability in the collecting duct occurs in two ways: a short-term regulation and a long-term adaptation. In congenital nephrogenic diabetes insipidus, the kidney does not respond to vasopressin. Ninety percent of these patients carry a mutation in the gene coding for the vasopressin V2 receptor located on the X chromosome. Autosomal recessive and dominant forms of nephrogenic diabetes insipidus that are caused by mutations in the aquaporin-2 gene have now been described. This review focuses on recent insight in the molecular and cellular defect in autosomal nephrogenic diabetes insipidus.