Titre | FRO: Role of VEGF-isoforms in pathological angiogenesis |
But | The aim of this project is to study the specific role of the VEGF-isoforms in pathological angiogenesis, and to investigate the effect of blocking a single isoform on formation of choroidal neovascularisation (CNV). |
Méthodes | VEGF-isoform specific mice (VEGF 120/+, VEGF 164/164 and VEGF188/188 mice) , as well as double transgenic mice (VEGF 120/164, VEGF 164/188 and VEGF120/188 mice) are used to study the role of VEGF-isoforms in pathological angiogenesis. In these mice models pathological angiogenesis is induced. CNV is induced by placing 3 laser spots at 9, 12 and 3 o’clock position (50µm, 0.05 s and 400mW). The amount of the new formed blood vessels is determined by FITC-dextrane perfusion. A fluorescent analysis of the whole mount choroids gives a threedimensional image of the vascular organization, remodeling and differentiation of the blood vessels. |
Résultats | The VEGF-isoform specific mice (VEGF 120/120, VEGF 164/164 and VEGF188/188 mice) were backcrossed to a C75Bl/6 background to be able to induce CNV and study the differential role of a single isoform on pathological angiogenesis. Subsequently, these mice will be intercrossed to obtain double transgenic mice to study the effect of blocking a single isoform on CNV production. Preliminary data will be presented at the OB-meeting 2008. |
Conclusion | This study will shed new light on the different role and the inhibition of the VEGF-isoforms in choroidal neovascularisation during age-related macular degeneration. Thus, our project may open new perspectives for the treatment of various retinopathies that are known to be associated with VEGF upregulation. |
Nom | VAN BERGEN |
Initiales | T |
Ville | Leuven |
Nom | VAN DE VEIRE |
Initiales | S |
Nom | MOONS |
Initiales | L |
Nom | STALMANS |
Initiales | I |