HCSP IN BETA-CELLS

The highly calcium-sensitive pool of granules in biphasic insulin secretion: Experimental and theoretical investigations

 Coordinatore LUNDS UNIVERSITET 

 Organization address address: Paradisgatan 5c
city: LUND
postcode: 22100

contact info
Titolo: Dr.
Nome: Lena
Cognome: Eliasson
Email: send email
Telefono: +46 40 391153
Fax: +46 40 391222

 Nazionalità Coordinatore Sweden [SE]
 Totale costo 136˙002 €
 EC contributo 136˙002 €
 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-2009-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-06-01   -   2012-01-12

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    LUNDS UNIVERSITET

 Organization address address: Paradisgatan 5c
city: LUND
postcode: 22100

contact info
Titolo: Dr.
Nome: Lena
Cognome: Eliasson
Email: send email
Telefono: +46 40 391153
Fax: +46 40 391222

SE (LUND) coordinator 136˙002.05

Mappa


 Word cloud

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experimental    hcsp    cells    beta    granules    calcium    model    biphasic    secretion    pancreatic    insulin    newcomer   

 Obiettivo del progetto (Objective)

'Insulin is released from the pancreatic beta-cells in a biphasic manner in response to a step in the ambient glucose concentration, and the loss of first-phase secretion is an early marker of diabetes. Studies have shown that there exist pools of insulin secretory granules with different calcium sensitivities. The project will study the nature, regulation and role of the highly calcium-sensitive pool (HCSP) in pancreatic beta-cells. Special focus will be on its relation to "newcomer granules", which fuse shortly after arriving to the membrane, during biphasic insulin secretion. We will apply a combination of well-established experimental methods such as patch-clamp techniques, life confocal and TIRF imaging, in novel combinations with knock-down of key exocytotic proteins, in particular Syntaxin and Synaptotagmin. The experimental part will be complemented and supported by modelling studies, building on our recently published model, which identified the HCSP with newcomer granules. This interdisciplinary project will test the model experimentally, and vice versa, use the model to suggest key experiments. The suggested work will complement the theoretical training of the fellow with hands-on experience.'

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