STING HOST DEFENCE
Elucidating the role of the protein STING in innate immunity to DNA and intracellular pathogens
| Coordinatore | THE PROVOST, FELLOWS, FOUNDATION SCHOLARS & THE OTHER MEMBERS OF BOARD OF THE COLLEGE OF THE HOLY & UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN
Organization address
address: College Green - contact info |
| Nazionalità Coordinatore | Ireland [IE] |
| Totale costo | 266˙722 € |
| EC contributo | 266˙722 € |
| 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-2011-IIF |
| Funding Scheme | MC-IIF |
| Anno di inizio | 0 |
| Periodo (anno-mese-giorno) | 0000-00-00 - 0000-00-00 |
Partecipanti
| # | ||||
|---|---|---|---|---|
| 1 |
THE PROVOST, FELLOWS, FOUNDATION SCHOLARS & THE OTHER MEMBERS OF BOARD OF THE COLLEGE OF THE HOLY & UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN
Organization address
address: College Green - contact info |
IE (DUBLIN) | coordinator | 266˙722.60 |
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Obiettivo del progetto (Objective)
'Infectious diseases kill 16 million people world-wide each year. Understanding how the immune system functions to sense and fight pathogens is essential for improving human health. A key host response to infection is the production of type I interferons (IFN). STING (Stimulator of IFN Genes) is a protein proposed to be essential for host type I IFN production in response to various intracellular pathogens including DNA and RNA viruses and bacteria. The reasons that STING may be involved in host defence against such a broad spectrum of pathogens is that STING is a critical player in the signalling pathway activated by cytosolic sensing of viral and bacterial DNA leading to type I IFN induction. Studies done in STING-deficient mice have demonstrated that STING is essential for host defence against viral infections. However the in vivo role of STING in intracellular bacterial pathogen infections is not clear. Moreover, it is not completely understood how and where STING activates type I IFN production in the cell. In this proposal, the Fellow will adopt biochemical and cell biology approaches to define the STING-mediated DNA sensing signalling pathway as well as the intracellular location(s) where signalling takes place (Objective A). The Fellow will use a conditional STING-deficient mouse that he recently generated to study the in vivo role of STING in host defence against intracellular pathogen infections (Objective B). This proposal is designed to utilize the strengths of both the Fellow and the Host lab to facilitate mutual transfer of knowledge and expertise for both parties. The host lab has a strong interest in studying the role of STING in sensing pathogen DNA, and the Fellow will provide the expertise and tools to allow these studies to bear fruit. In turn, the Fellow will obtain knowledge and technical expertise in a world-class innate immunity lab, which will help him expand his research network, attain an independent position and advance his career.'