CPAF

Calcium Propagation in Atrial Fibrillation

 Coordinatore KATHOLIEKE UNIVERSITEIT LEUVEN 

 Organization address address: Oude Markt 13
city: LEUVEN
postcode: 3000

contact info
Titolo: Dr.
Nome: Delauré
Cognome: Stijn
Email: send email
Telefono: -1248
Fax: -506

 Nazionalità Coordinatore Belgium [BE]
 Totale costo 166˙800 €
 EC contributo 166˙800 €
 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) 2010-03-01   -   2012-02-29

 Partecipanti

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

 Organization address address: Oude Markt 13
city: LEUVEN
postcode: 3000

contact info
Titolo: Dr.
Nome: Delauré
Cognome: Stijn
Email: send email
Telefono: -1248
Fax: -506

BE (LEUVEN) coordinator 166˙800.00

Mappa


 Word cloud

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

af    reticulum    sarcoplasmic    arrhythmias    imaging    release    ca    receptors    dhprs    ryrs    dyads    channels    myocytes    organization    ryr   

 Obiettivo del progetto (Objective)

'Synchronized release of Ca2 from the internal Ca2 store of cardiac myocytes, the sarcoplasmic reticulum, is essential for a normal heart beat. This is obtained through a sophisticated subcellular organization, the dyad. In dyads, a cluster of release channels in the sarcoplasmic reticulum, ryanodine receptors or RyRs, face Ca2 channels in the cell membrane, the dihydropyrydine receptors or DHPRs. DHPRs provide the Ca2 influx that triggers opening of RyR. Ca2 release can also propagate between RyR, leading to Ca2 waves that can initiate arrhythmias. We hypothesize that RyR that are not within dyads have different properties that may facilitate wave-like propagation and arrhythmias. The objectives are (1) to identify and characterize RyR located between dyads in the sarcomeric space in healthy myocytes (2) to establish whether altered organization and properties of RyRs in chronic atrial fibrillation (AF) contribute to the contractile dysfunction and arrhythmia in AF. My stay in the host lab will provide a clinical and translational perspective to my current knowledge enhancing the potential impact of my research. An interdisciplinary approach for imaging of RyR with access to novel microscopic techniques in the Molecular engineering department and tools for image analysis with the Medical Imaging Center and ESAT will enhance my technological expertise.'

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