WNT_IMMUNE

WNT3A IN NEUROIMMUNE INTERACTIONS IN STROKE BRAIN

 Coordinatore THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE 

 Organization address address: The Old Schools, Trinity Lane
city: CAMBRIDGE
postcode: CB2 1TN

contact info
Titolo: Ms.
Nome: Renata
Cognome: Schaeffer
Email: send email
Telefono: +44 1223 333543
Fax: +44 1223 332988

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 221˙606 €
 EC contributo 221˙606 €
 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-2013-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2015
 Periodo (anno-mese-giorno) 2015-01-12   -   2017-01-11

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE

 Organization address address: The Old Schools, Trinity Lane
city: CAMBRIDGE
postcode: CB2 1TN

contact info
Titolo: Ms.
Nome: Renata
Cognome: Schaeffer
Email: send email
Telefono: +44 1223 333543
Fax: +44 1223 332988

UK (CAMBRIDGE) coordinator 221˙606.40

Mappa


 Word cloud

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brain    wnt    adult    neurogenesis    bm    cells    vivo    stroke    immune   

 Obiettivo del progetto (Objective)

'A stroke, or cerebrovascular accident, is the rapid loss of brain function due to disturbance in the blood supply to the brain. Ischemic stroke is currently the leading cause of adult chronic disability, the second most common cause of cognitive impairment and the third most frequent cause of mortality in industrialised countries. Consequently, it is presently of outmost importance to study, to understand and to characterize the etiopathological mechanisms underlying stroke.

Neuroinflammation is undoubtedly linked to stroke and many other neurological disorders, since immune response impacts on the diseased nervous system modulating the progression of them. Neuroimmune interactions constitute an important part of this immune response and they seem to control several regenerative processes in the brain, including neurogenesis. This crosstalk is mediated by different molecules and among them, Wnt proteins have emerged as interesting modulators. We here propose to analyze the putative neuroprotective role of a specific immune-secreted Wnt subtype, Wnt3a, in stroke, as well as the effects of this ligand on adult neurogenesis processes.

The project will include two different approaches: a first in vitro part to isolate, characterize and modify with lentiviral constructions Bone-Marrow (BM) derived cells in order to overexpress or to abolish Wnt3a expression. A second in vivo part to generate chimeric mice by transplantation into the brain of the previously modified BM derived cells.

This fellowship will give important information on the role of Wnt3a in stroke as well as providing a powerful in vivo tool and will open direct leads for therapeutics. I will acquire a more complete and diversified scientific knowledge and technical preparation through a multi-disciplinary approach, and will be trained to become an expert researcher towards an independent research career in the field of neuroscience'

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