AQUASHUTTLE

Regulation of endocytosis of the aquaporin-2 water channel: an interplay of phosphorylation and ubiquitination

 Coordinatore STICHTING KATHOLIEKE UNIVERSITEIT 

 Organization address address: GEERT GROOTEPLEIN NOORD 9
city: NIJMEGEN
postcode: 6525 EZ

contact info
Titolo: Mr.
Nome: Maarten
Cognome: Van Langen
Email: send email
Telefono: +31 24 3619791
Fax: +31 24 3540529

 Nazionalità Coordinatore Netherlands [NL]
 Totale costo 176˙685 €
 EC contributo 176˙685 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2010-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-09-01   -   2013-08-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    STICHTING KATHOLIEKE UNIVERSITEIT

 Organization address address: GEERT GROOTEPLEIN NOORD 9
city: NIJMEGEN
postcode: 6525 EZ

contact info
Titolo: Mr.
Nome: Maarten
Cognome: Van Langen
Email: send email
Telefono: +31 24 3619791
Fax: +31 24 3540529

NL (NIJMEGEN) coordinator 176˙685.60

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

dub    atp    decreased    regulation    shuttling    homeostasis    avp       renal    plasma    water    ubiquitination    endocytosis    ligase    humans    reabsorption    dopamine    kidney    aqp    disorders    phosphorylation    ndi    membrane    expression    ubiquitin    balance    data    exocytosis    ps      

 Obiettivo del progetto (Objective)

'A proper water balance is essential for life on land and is, besides drinking water, depending on water reabsorption in the kidney. Renal water uptake depends on the expression of the aquaporin-2 (AQP2) water channel in the urinary membrane of collecting duct cells, which is critically determined by a balance of shuttling of AQP2 to (exocytosis) and from (endocytosis) this membrane. Humans with insufficient AQP2 levels suffer from Nephrogenic diabetes insipidus (NDI), a disorder in which the kidney cannot concentrate urine resulting in polyuria, while humans with increased plasma membrane abundance of AQP2 excessively reabsorb water. The shuttling of AQP2 is under hormonal regulation. Recent data showed that vasopressin (AVP) induces AQP2 exocytosis by increasing its phosphorylation at serine 256 (pS256), S264 and S269, whereas pS261 was decreased. AVP-counteracting hormones, such as dopamine and ATP, induce AQP2 endocytosis involving its temporary ubiquitination at lysine 270 (K270). The effect on changes in pS256/261/264/269, and the identity of the E3 ubiquitin ligase and deubiquitinating enzyme (DUB) are unknown. Using an ideal polarized cell model and state of the art tools and techniques, the applicant will (1) determine the relationship and order in changes in pS256/261/264/269 and ubiquitination with dopamine/ATP-induced endocytosis of AQP2, (2) investigate whether the plasma membrane expression of constitutively-phosphorylated S269 is due to decreased K270 ubiquitination, (3) search for and identify the E3 ubiquitin ligase and DUB regulating AQP2 endocytosis, and (4) investigate in what sense a mutation causing NDI (AQP2-P262L) is changed in its phosphorylation compared to wt-AQP2 and whether it explains its missorting. The anticipated data will increase the insight into the dynamic regulation of renal water reabsorption and plasma membrane expression of AQP2 in health and disease, and may reveal new targets for treatment of water balance disorders.'

Introduzione (Teaser)

Water homeostasis in the body is maintained by kidneys. Unravelling the regulatory system that controls renal water reabsorption could have clinical implications for disorders presenting with abnormal water homeostasis.

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