Skip to main content
Aller à la page d’accueil de la Commission européenne (s’ouvre dans une nouvelle fenêtre)
français fr
CORDIS - Résultats de la recherche de l’UE
CORDIS
Contenu archivé le 2024-05-29

Molecular imaging of stem cell differentiation

Objectif

Magnetic Resonance contrast agents for non-invasive monitoring of the differentiation of embryonic stem cells into brain cells will be developed and tested in an animal model. These contrast agents (CA) will revolutionise our understanding of cellular differentiation processes by visualising "cells at work" in vivo with high spatial and temporal resolution. In contrast to other molecular imaging techniques, magnetic resonance imaging (MRI) is not limited to invasive ex vivo studies or the outermost layer o f biological tissue like optical techniques.

Chelated Gadolinium-based MRI CAs will be designed and synthesised so that enzymes specifically expressed after the differentiation of stem cells will generate a contrast by activating the `silent¿ CA through chemical modification. No transfection of cells is required for visualisation. In order to address a variety of differentiation processes, a number of different CAs will be generated, which focus on enzymes responsible for the synthesis of neurotransmitters, but also compounds that distinguish between neuronal and astrocyte metabolism. Contrast agents will be synthesised and provided by the laboratory of Prof S Aime (University Torino).

Methodological issues of the design and testing of CA that will be addressed in this project are:
1) optimisation of the internalisation,
2) specificity of the enzyme activity for the activation of the CA and
3) maximisation of the generated contrast (increased sensitivity).

CAs will first be tested on in vitro differentiated cultures of embryonal stem cells (L1 and D3 mouse stem cells) and then in animal models. Animal models utilised for the implantation are normal rats and models developed in the host laboratory for stroke and tumour. As the concept is universally applicable for visualisation of cell differentiation, it will improve high resolution in vivo monitoring of cell function also for models in other organs, other disease models and replacement therapy in humans.

Champ scientifique (EuroSciVoc)

Thème(s)

Appel à propositions

FP6-2002-MOBILITY-12
Voir d’autres projets de cet appel

Régime de financement

IRG - Marie Curie actions-International re-integration grants

Coordinateur

MAX-PLANCK-GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN E.V.
Contribution de l’UE
Aucune donnée
Coût total
Aucune donnée