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Am J Physiol Renal Physiol
2009 Aug 01;2972:F489-98. doi: 10.1152/ajprenal.90589.2008.
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Characterization of D150E and G196D aquaporin-2 mutations responsible for nephrogenic diabetes insipidus: importance of a mild phenotype.
Guyon C
,
Lussier Y
,
Bissonnette P
,
Leduc-Nadeau A
,
Lonergan M
,
Arthus MF
,
Perez RB
,
Tiulpakov A
,
Lapointe JY
,
Bichet DG
.
???displayArticle.abstract??? Aquaporin-2 (AQP2) is a water channel responsible for the final water reabsorption in renal collecting ducts. Alterations in AQP2 function induce nephrogenic diabetes insipidus (NDI), a condition characterized by severe polyuria and polydipsia. Three patients affected with severe NDI, who were compound heterozygous for the AQP2 mutations D150E and G196D, are presented here along with a mildly affected D150E homozygous patient from another family. Using Xenopus oocytes as an expression system, these two mutations (G196D and D150E) were compared with the wild-type protein (AQP2-wt) for functional activity (water flux analysis), protein maturation, and plasma membrane targeting. AQP2-wt induces a major increase in water permeability (P(f) = 47.4 +/- 12.2 x 10(-4) cm/s) whereas D150E displays intermediate P(f) values (P(f) = 12.5 +/- 3.0 x 10(-4) cm/s) and G196D presents no specific water flux, similar to controls (P(f) = 2.1 +/- 0.8 x 10(-4) cm/s and 2.2 +/- 0.7 x 10(-4) cm/s, respectively). Western blot and immunocytochemical evaluations show protein targeting that parallels activity levels with AQP2-wt adequately targeted to the plasma membrane, partial targeting for D150E, and complete sequestration of G196D within intracellular compartments. When coinjecting AQP2-wt with mutants, no (AQP2-wt + D150E) or partial (AQP2-wt + G196D) reduction of water flux were observed compared with AQP2-wt alone, whereas complete loss of function was found when both mutants were coinjected. These results essentially recapitulate the clinical profiles of the family members, showing a typical dominant negative effect when G196D is coinjected with either AQP2-wt or D150E but not between AQP2-wt and D150E mutant.
Agre,
The aquaporin family of water channels in kidney.
1996, Pubmed,
Xenbase
Agre,
The aquaporin family of water channels in kidney.
1996,
Pubmed
,
Xenbase
Bichet,
Nephrogenic diabetes insipidus.
1998,
Pubmed
Bissonnette,
Functional expression of tagged human Na+-glucose cotransporter in Xenopus laevis oocytes.
1999,
Pubmed
,
Xenbase
Buck,
Evidence for stabilization of aquaporin-2 folding mutants by N-linked glycosylation in endoplasmic reticulum.
2004,
Pubmed
,
Xenbase
Deen,
Nephrogenic diabetes insipidus.
2000,
Pubmed
de Mattia,
Lack of arginine vasopressin-induced phosphorylation of aquaporin-2 mutant AQP2-R254L explains dominant nephrogenic diabetes insipidus.
2005,
Pubmed
Duquette,
Local osmotic gradients drive the water flux associated with Na(+)/glucose cotransport.
2001,
Pubmed
,
Xenbase
Frøkiaer,
Pathophysiology of aquaporin-2 in water balance disorders.
1998,
Pubmed
Fujiwara,
Molecular biology of hereditary diabetes insipidus.
2005,
Pubmed
Goji,
Novel mutations in aquaporin-2 gene in female siblings with nephrogenic diabetes insipidus: evidence of disrupted water channel function.
1998,
Pubmed
,
Xenbase
Hendriks,
Glycosylation is important for cell surface expression of the water channel aquaporin-2 but is not essential for tetramerization in the endoplasmic reticulum.
2004,
Pubmed
Iolascon,
Characterization of two novel missense mutations in the AQP2 gene causing nephrogenic diabetes insipidus.
2007,
Pubmed
Kamsteeg,
Importance of aquaporin-2 expression levels in genotype -phenotype studies in nephrogenic diabetes insipidus.
2000,
Pubmed
,
Xenbase
Kamsteeg,
Defective processing and trafficking of water channels in nephrogenic diabetes insipidus.
2000,
Pubmed
Kamsteeg,
The subcellular localization of an aquaporin-2 tetramer depends on the stoichiometry of phosphorylated and nonphosphorylated monomers.
2000,
Pubmed
,
Xenbase
Kamsteeg,
An impaired routing of wild-type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus.
1999,
Pubmed
,
Xenbase
Kuwahara,
Three families with autosomal dominant nephrogenic diabetes insipidus caused by aquaporin-2 mutations in the C-terminus.
2001,
Pubmed
,
Xenbase
Leduc-Nadeau,
Elaboration of a novel technique for purification of plasma membranes from Xenopus laevis oocytes.
2007,
Pubmed
,
Xenbase
Lin,
Two novel aquaporin-2 mutations responsible for congenital nephrogenic diabetes insipidus in Chinese families.
2002,
Pubmed
,
Xenbase
Marr,
Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidus.
2002,
Pubmed
,
Xenbase
Mulders,
An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex.
1998,
Pubmed
,
Xenbase
Nielsen,
Aquaporins in the kidney: from molecules to medicine.
2002,
Pubmed
Nielsen,
Physiology and pathophysiology of renal aquaporins.
1999,
Pubmed
Tamarappoo,
Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones.
1998,
Pubmed
,
Xenbase
Umenishi,
Effect on stability, degradation, expression, and targeting of aquaporin-2 water channel by hyperosmolality in renal epithelial cells.
2005,
Pubmed
van Balkom,
Hypertonicity is involved in redirecting the aquaporin-2 water channel into the basolateral, instead of the apical, plasma membrane of renal epithelial cells.
2003,
Pubmed
Wagner,
The use of Xenopus laevis oocytes for the functional characterization of heterologously expressed membrane proteins.
2000,
Pubmed
,
Xenbase
Zeuthen,
Water transport by the Na+/glucose cotransporter under isotonic conditions.
1997,
Pubmed
,
Xenbase