WOUNDHEALINGEGF

The role of EGF/ERK signaling pathway during the wound healing response in Drosophila and zebrafish epithelia

 Coordinatore INSTITUTO DE MEDICINA MOLECULAR 

 Organization address address: AVENIDA PROF EGAS MONIZ
city: LISBOA
postcode: 1649 028

contact info
Titolo: Dr.
Nome: Margarida
Cognome: Pinto Gago
Email: send email
Telefono: 351218000000
Fax: 351218000000

 Nazionalità Coordinatore Portugal [PT]
 Totale costo 146˙783 €
 EC contributo 146˙783 €
 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) 2010-09-01   -   2012-08-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    INSTITUTO DE MEDICINA MOLECULAR

 Organization address address: AVENIDA PROF EGAS MONIZ
city: LISBOA
postcode: 1649 028

contact info
Titolo: Dr.
Nome: Margarida
Cognome: Pinto Gago
Email: send email
Telefono: 351218000000
Fax: 351218000000

PT (LISBOA) coordinator 146˙783.60

Mappa


 Word cloud

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pathways    wound    epithelia    cell    signaling    healing    primary    mechanisms    signals    cascades    embryonic   

 Obiettivo del progetto (Objective)

'Epithelia act as physical barriers that protect living organisms from the surrounding environment. Therefore, the organization and homeostasis in epithelial tissues requires robust mechanisms that assure their integrity in a variety of biological situations, such as normal cell turnover, inflammation and injury. The cell biology of wound healing has started to be understood but there are still many open questions and the signaling cascades that regulate this process are largely unknown. An intriguing and crucial question is what is the nature of the earliest signals that activate the different events of a wound response. In this project, we will study the signaling pathways required for the activation of the wound response. Our main focus will be the role of EGF/ERK signaling, which we propose to be one of the first pathways to be activated in this process. We also plan to determine the primary signals activating the wound response cascades. We will use the Drosophila embryonic and pupal epithelia as our primary model systems, but will also investigate whether these signaling mechanisms are conserved in vertebrates, by studying the wound healing process in zebrafish embryonic epithelia.'

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