PTPS IN ANGIOGENESIS

Role of protein-tyrosine phosphatases in angiogenesis

 Coordinatore Novartis Forschungsstiftung 

 Organization address address: Maulbeerstrasse 66
city: BASEL
postcode: 4058

contact info
Titolo: Ms.
Nome: Dorothy
Cognome: Searles
Email: send email
Telefono: -6973002
Fax: -6973996

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 0 €
 EC contributo 180˙801 €
 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-IEF-2008
 Funding Scheme MC-IEF
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-07-01   -   2011-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    Novartis Forschungsstiftung

 Organization address address: Maulbeerstrasse 66
city: BASEL
postcode: 4058

contact info
Titolo: Ms.
Nome: Dorothy
Cognome: Searles
Email: send email
Telefono: -6973002
Fax: -6973996

CH (BASEL) coordinator 180˙801.44

Mappa


 Word cloud

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angiogenesis    ptks    ptps    cells    tyrosine    endothelial    protein    angiogenic    pathological    function    inducible   

 Obiettivo del progetto (Objective)

'Angiogenesis is the formation of new blood vessels from pre-existing ones and is involved in different physiological and pathological processes such as cancer and ischemia. Tyrosine phosphorylation is a reversible process, mediated by protein-tyrosine kinases (PTKs) and protein-tyrosine phosphatases (PTPs). Although the role of PTKs in angiogenesis is well established, little is known about the function of specific PTPs in this process. In collaboration with Dr. H. Augustin, (Heidelberg, Germany) we found that the expression of several PTPs changes when spheroids of endothelial cells embedded in 3D matrices are exposed to angiogenic stimuli. To investigate the role of PTPs in angiogenesis, we generated a tetracycline-inducible shRNA library for targeting PTPs. We are also generating lentiviral vectors expressing inducible cDNAs of all the human PTPs. I propose to investigate the biological role of PTPs in angiogenesis by loss- and gain of function experiments in endothelial cells, using different in vitro and in vivo angiogenesis assays. My studies will determine the role of PTPs in developmental and pathological angiogenesis and test their merits as targets of angiogenic therapy.'

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