A PrPC-caveolin-Lyn complex negatively controls neuronal GSK3β and serotonin 1B receptor

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Hernandez-Rapp, Julia | Martin-Lannerée, Séverine | Hirsch, Théo | Pradines, Elodie | Alleaume-Butaux, Aurélie | Schneider, Benoît | Baudry, Anne | Launay, Jean-Marie | Mouillet-Richard, Sophie

Edité par CCSD ; Nature Publishing Group -

International audience. The cellular prion protein, PrPC, is a glycosylphosphatidylinositol-anchored protein, abundant in lipid rafts and highly expressed in the brain. While PrPC is much studied for its involvement under its abnormal PrPSc isoform in Transmissible Spongiform Encephalopathies, its physiological role remains unclear. Here, we report that GSK3β, a multifunctional kinase whose inhibition is neuroprotective, is a downstream target of PrPC signalling in serotonergic neuronal cells. We show that the PrPC-dependent inactivation of GSK3β is relayed by a caveolin-Lyn platform located on neuronal cell bodies. Furthermore, the coupling of PrPC to GSK3β potentiates serotonergic signalling by altering the distribution and activity of the serotonin 1B receptor (5-HT1BR), a receptor that limits neurotransmitter release. In vivo, our data reveal an increased GSK3β kinase activity in PrP-deficient mouse brain, as well as sustained 5-HT1BR activity, whose inhibition promotes an anxiogenic behavioural response. Collectively, our data unveil a new facet of PrPC signalling that strengthens neurotransmission.

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