STEPS

Signalling compartmentalization and vesicle Trafficking at the Phagocytic Synapses

 Coordinatore UNIVERSITA DEGLI STUDI DI PADOVA 

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 Nazionalità Coordinatore Italy [IT]
 Totale costo 2˙350˙342 €
 EC contributo 2˙350˙342 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2012-ADG_20120314
 Funding Scheme ERC-AG
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-04-01   -   2018-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    HUMANITAS MIRASOLE SPA

 Organization address address: "Via Manzoni, 56"
city: ROZZANO-MILAN
postcode: 20089

contact info
Titolo: Dr.
Nome: Danilo
Cognome: Petroni
Email: send email
Telefono: +39 02 8224 2435
Fax: +39 02 8224 5191

IT (ROZZANO-MILAN) beneficiary 343˙720.34
2    UNIVERSITA DEGLI STUDI DI PADOVA

 Organization address address: VIA 8 FEBBRAIO 2
city: PADOVA
postcode: 35122

contact info
Titolo: Ms.
Nome: Luisa
Cognome: Caldon
Email: send email
Telefono: +39 049 827 6032

IT (PADOVA) hostInstitution 2˙006˙621.60
3    UNIVERSITA DEGLI STUDI DI PADOVA

 Organization address address: VIA 8 FEBBRAIO 2
city: PADOVA
postcode: 35122

contact info
Titolo: Prof.
Nome: Antonella
Cognome: Viola
Email: send email
Telefono: +39 049 8276047
Fax: +39 049 8276049

IT (PADOVA) hostInstitution 2˙006˙621.60

Mappa


 Word cloud

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

cell    signalling    molecular    responses    macrophage    context    receptors    particle    plasma    receptor    phagocytic    synapse    infectious    pathways    immune    membrane    macrophages   

 Obiettivo del progetto (Objective)

'A key feature of the immune response is its specificity and macrophages must be able to discriminate precisely between an infectious stimulus and a non-infectious one and tune their response in accordance with the molecular context in which the target particle is recognized. In recent years, scientists have proposed the concept of the phagocytic synapse, to stress the fact that a particle does not engage only one receptor on the cell surface; instead, an array of receptors interacts with a specific pathogen, either sequentially or simultaneously. Indeed, the tightly controlled and specific responses of macrophages require the establishing of checkpoints for signalling and the phagocytic synapse represent an exquisite site for cross-talk among several signalling pathways. Although we can describe detailed signalling pathways for most of the single receptors acting at the phagocytic synapse, we still do not know how these pathways are integrated during the various phases of macrophage responses. An integrated view of phagocytic synapse signalling would allow us to understand the contribution of each ligand-receptor pair to macrophage dysfunctions in pathology and to design novel immunotherapeutic strategies. The aim of STePS is to provide a deeper understanding of the molecular interactions leading to the orchestration of phagocytic synapses for phagocytosis and activation, two events crucial for immune responses to pathogens as well as for inflammation. In particular, we will focus on three fundamental aspects that bring together the fields of immunology and cell biology: establishment of dynamic platforms for recognition and signalling at the plasma membrane; vesicle trafficking to the plasma membrane; signalling compartmentalization for specific cell functions. Importantly, these mechanisms will be analyzed in the context of physiological and pathological conditions, thus providing answers to both basic and translational biomedical research questions.'

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