Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
Proc Natl Acad Sci U S A
2003 Mar 04;1005:2945-50. doi: 10.1073/pnas.0437994100.
Show Gene links
Show Anatomy links
Aquaglyceroporin AQP9: solute permeation and metabolic control of expression in liver.
Carbrey JM
,
Gorelick-Feldman DA
,
Kozono D
,
Praetorius J
,
Nielsen S
,
Agre P
.
???displayArticle.abstract???
Aquaglyceroporins form the subset of the aquaporin water channel family that is permeable to glycerol and certain small, uncharged solutes. AQP9 has unusually broad solute permeability and is expressed in hepatocyte plasma membranes. Proteoliposomes reconstituted with expressed, purified rat AQP9 protein were compared with simple liposomes for solute permeability. At pH 7.5, AQP9 proteoliposomes exhibited Hg(2+)-inhibitable glycerol and urea permeabilities that were increased 63-fold and 90-fold over background. beta-Hydroxybutyrate permeability was not increased above background, and osmotic water permeability was only minimally elevated. During starvation, the liver takes up glycerol for gluconeogenesis. Expression of AQP9 in liver was induced up to 20-fold in rats fasted for 24-96 h, and the AQP9 level gradually declined after refeeding. No changes in liverAQP9 levels were observed in rats fed ketogenic diets or high-protein diets, but AQP9 levels were elevated in livers of rats made diabetic by streptozotocin injection. When blood glucose levels of the diabetic rats were restored to normal by insulin treatments, the AQP9 levels returned to baseline. Confocal immunofluorescence revealed AQP9 immunostaining on the sinusoidal surfaces of hepatocyte plates throughout the livers of control rats. Denser immunostaining was observed in the same distribution in livers of fasted and streptozotocin-treated rats. We conclude that AQP9 serves as membrane channel in hepatocytes for glycerol and urea at physiological pH, but not for beta-hydroxybutyrate. In addition, levels of AQP9 expression fluctuate depending on the nutritional status of the subject and the circulating insulin levels.
Agre,
The aquaporins, blueprints for cellular plumbing systems.
1998, Pubmed
Agre,
The aquaporins, blueprints for cellular plumbing systems.
1998,
Pubmed
Baba,
Glycerol gluconeogenesis in fasting humans.
1995,
Pubmed
Borgnia,
Reconstitution and functional comparison of purified GlpF and AqpZ, the glycerol and water channels from Escherichia coli.
2001,
Pubmed
Elkjaer,
Immunolocalization of AQP9 in liver, epididymis, testis, spleen, and brain.
2000,
Pubmed
Exton,
Regulation of gluconeogenesis by glucocorticoids.
1979,
Pubmed
Gabbay,
Insulin regulation of phosphoenolpyruvate carboxykinase gene expression does not require activation of the Ras/mitogen-activated protein kinase signaling pathway.
1996,
Pubmed
Halestrap,
The proton-linked monocarboxylate transporter (MCT) family: structure, function and regulation.
1999,
Pubmed
,
Xenbase
Haughton,
Insulin replacement therapy for the rat model of streptozotocin-induced diabetes mellitus.
1999,
Pubmed
Ishibashi,
Molecular cloning and expression of a member of the aquaporin family with permeability to glycerol and urea in addition to water expressed at the basolateral membrane of kidney collecting duct cells.
1994,
Pubmed
,
Xenbase
Ishibashi,
Cloning and functional expression of a new water channel abundantly expressed in the testis permeable to water, glycerol, and urea.
1997,
Pubmed
,
Xenbase
Kishida,
Genomic structure and insulin-mediated repression of the aquaporin adipose (AQPap), adipose-specific glycerol channel.
2001,
Pubmed
Kishida,
Aquaporin adipose, a putative glycerol channel in adipocytes.
2000,
Pubmed
Ko,
Cloning and functional expression of rAOP9L a new member of aquaporin family from rat liver.
1999,
Pubmed
,
Xenbase
Kondo,
Human aquaporin adipose (AQPap) gene. Genomic structure, promoter analysis and functional mutation.
2002,
Pubmed
,
Xenbase
Kuriyama,
Molecular cloning and expression of a novel human aquaporin from adipose tissue with glycerol permeability.
1997,
Pubmed
,
Xenbase
Kuriyama,
Coordinated regulation of fat-specific and liver-specific glycerol channels, aquaporin adipose and aquaporin 9.
2002,
Pubmed
Laemmli,
Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
1970,
Pubmed
Leino,
Diet-induced ketosis increases monocarboxylate transporter (MCT1) levels in rat brain.
2001,
Pubmed
Neely,
Heterotetrameric composition of aquaporin-4 water channels.
1999,
Pubmed
,
Xenbase
Nicchia,
Tissue distribution and membrane localization of aquaporin-9 water channel: evidence for sex-linked differences in liver.
2001,
Pubmed
Nihei,
Immunolocalization of aquaporin-9 in rat hepatocytes and Leydig cells.
2001,
Pubmed
Peroni,
Measuring glycerol turnover, gluconeogenesis from glycerol, and total gluconeogenesis with [2-13C] glycerol: role of the infusion-sampling mode.
1996,
Pubmed
Peroni,
Measuring gluconeogenesis with [2-13C]glycerol and mass isotopomer distribution analysis of glucose.
1995,
Pubmed
Preston,
Appearance of water channels in Xenopus oocytes expressing red cell CHIP28 protein.
1992,
Pubmed
,
Xenbase
Saparov,
Water and ion permeation of aquaporin-1 in planar lipid bilayers. Major differences in structural determinants and stoichiometry.
2001,
Pubmed
Smith,
Facilitative urea transporters.
2001,
Pubmed
Tsukaguchi,
Molecular characterization of a broad selectivity neutral solute channel.
1998,
Pubmed
,
Xenbase
Tsukaguchi,
Functional and molecular characterization of the human neutral solute channel aquaporin-9.
1999,
Pubmed
,
Xenbase
Vajda,
Delayed onset of brain edema and mislocalization of aquaporin-4 in dystrophin-null transgenic mice.
2002,
Pubmed