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STING signalling modulation via the Electron Transport Chain

Descrizione del progetto

Metabolismo cellulare e segnalazione del sistema immunitario innato

L’immunometabolismo, come ambito di ricerca, fornisce nuove intuizioni sull’interazione dinamica tra il sistema immunitario (immunità) e i processi metabolici di un organismo. Gli adattamenti metabolici sono fondamentali per le risposte immunitarie. Con il progressivo aumento della nostra comprensione dell’immunometabolismo, il meccanismo di segnalazione STING sta ricevendo sempre più attenzione. La risposta immunitaria innata al dsDNA citosolico attraverso il percorso cGAS-STING si è dimostrata essenziale nella risposta a varie infezioni virali, batteriche e parassitarie, nell’autoimmunità e nel cancro. Il progetto STIMULATE, finanziato dall’UE, si concentrerà sulla relazione tra il metabolismo cellulare e la segnalazione del sistema immunitario innato mediante STING. In particolare, utilizzerà un approccio proteomico imparziale così come approcci mirati di immunometabolismo per trovare le vie metaboliche modulanti STING.

Obiettivo

The innate immune response to cytosolic dsDNA via the cGAS-STING pathway has been shown to be essential in the response to various viral, bacterial and parasitic infections, in autoimmunity and in cancer. However, the relationship between STING signalling and metabolism is currently unknown. In recent years, our understanding of immunometabolism has also increased – it is becoming clear that metabolic adaptations are fundamental for immune responses. Due to its role in this wide range of clinical pathologies, the mechanism of STING signalling has received a great deal of scientific interest and several STING-targeting compounds are now reaching clinical trial stages of development. It is therefore important to understand the effect of STING activation on mammalian cells, as well as how to manipulate this response to the greatest effect. The research proposed here focuses on the relationship between cellular metabolism and innate immune signalling via STING, using an unbiased proteomics approach as well as targeted immunometabolism approaches to find STING modulating metabolic pathways.
Having completed my PhD studies in immunology, I am pursuing a postdoctoral project, in the lab of Dr. David Sancho at the CNIC, that utilises my expertise and allows me to expand my technical horizons and enhance my career development. As an expert in innate immune signalling I believe that combining my knowledge with the Sancho lab’s expertise in cellular immunobiology and metabolism will lead to a better understanding of our immune system. As well as the expertise of my host lab, I will also benefit from the collaboration of leaders in proteomics and mitochondrial biology. This Individual Fellowship would greatly benefit my current research objectives and my career as a whole by allowing me to explore my research interests in a supportive environment, where I will receive the training required for the next stage of my research career.

Coordinatore

CENTRO NACIONAL DE INVESTIGACIONES CARDIOVASCULARES CARLOS III (F.S.P.)
Contribution nette de l'UE
€ 160 932,48
Indirizzo
CALLE MELCHOR FERNANDEZ ALMAGRO 3
28029 Madrid
Spagna

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Regione
Comunidad de Madrid Comunidad de Madrid Madrid
Tipo di attività
Research Organisations
Collegamenti
Costo totale
€ 160 932,48