Objectif Understanding how cellular activation occurs in complex signaling networks is an important challenge in particular in multi-genic diseases such as autoimmune disease, type II diabetes, and cancer. A critical component of signaling complexity is that proteins inside live cells enrich at particular locations and times. Co-enrichment of two proteins enhances their interaction efficiency. At the systems scale, such patterning thus determines how regulatory information flows through signaling networks. We have developed approaches to harness the regulatory information encoded in systems scale spatiotemporal distributions to understand cell function, using live cell time-lapse fluorescence microscopy in imaging of the activation of primary T cells (> 50 signaling intermediates, > 10,000 cell couples). Upon transfer to the University of Bristol, we will further develop these unique approaches and apply them to understand T cell function in health and disease with two objectives.The first, methodological objective is to further develop quantitative systems scale imaging approaches, including computational image analysis and mathematical modeling, resulting in generally applicable tools for the analysis of complex signaling systems. The second, biological objective is to elucidate how the spatiotemporal organization of T cell signaling regulates lymphocyte function. By causally linking the spatiotemporal organization of signaling to cell function, we will investigate roles of the tyrosine kinases Itk and Tec as established regulators of the spatiotemporal organization of T cell signaling (Singleton et al., Sci. Signal., 2011) in cytokine secretion, primary immunodeficiency, and Leishmania infection, T cell actin regulation by the central costimulatory receptor CD28, signaling in the killing of virally-infected and tumor target cells by cytotoxic T cells and natural killer cells, and SLAM receptors in susceptibility to the autoimmune disease systemic lupus erythematosus. Champ scientifique natural sciencesbiological sciencescell biologycell signalingnatural sciencesbiological sciencesbiochemistrybiomoleculesproteinsmedical and health sciencesclinical medicineendocrinologydiabetesmedical and health sciencesbasic medicineimmunologyautoimmune diseasesmedical and health sciencesclinical medicineoncology Programme(s) FP7-PEOPLE - Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) Thème(s) FP7-PEOPLE-2012-CIG - Marie-Curie Action: "Career Integration Grants" Appel à propositions FP7-PEOPLE-2012-CIG Voir d’autres projets de cet appel Régime de financement MC-CIG - Support for training and career development of researcher (CIG) Coordinateur UNIVERSITY OF BRISTOL Contribution de l’UE € 100 000,00 Adresse BEACON HOUSE QUEENS ROAD BS8 1QU Bristol Royaume-Uni Voir sur la carte Région South West (England) Gloucestershire, Wiltshire and Bristol/Bath area Bristol, City of Type d’activité Higher or Secondary Education Establishments Contact administratif Sarah Everett-Cox (Mrs.) Liens Contacter l’organisation Opens in new window Site web Opens in new window Coût total Aucune donnée
