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This project allows the interrogation of mechanisms in both murine models and human tissue

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Thus, we tested here whether increased VEGFA expression specifically in the RPE (and not in the retina or circulation) is sufficient to induce RPE barrier breakdown and neovascular AMDlike pathologies, by generating mice that overexpress VEGFA only in the RPE postnatally (Vmd2Cre +/WT /ROSASTOP fl/fl VEGFA 164 mice)

However, the identity of the kinase responsible for the priming phosphorylation at S114 and the precise mechanism by which this modification triggers protein turnover remains unclear

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