TY - JOUR
T1 - A PrPC -caveolin-Lyn complex negatively controls neuronal GSK3β and serotonin 1B receptor
AU - Hernandez-Rapp, Julia
AU - Martin-Lannerée, Séverine
AU - Hirsch, Théo Z.
AU - Pradines, Elodie
AU - Alleaume-Butaux, Aurélie
AU - Schneider, Benoît
AU - Baudry, Anne
AU - Launay, Jean Marie
AU - Mouillet-Richard, Sophie
N1 - Publisher Copyright:
© 2014, Nature Publishing Group. All rights reserved.
PY - 2015/4/1
Y1 - 2015/4/1
N2 - 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-HT 1BR), 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-HT 1BR activity, whose inhibition promotes an anxiogenic behavioural response. Collectively, our data unveil a new facet of PrPC signalling that strengthens neurotransmission.
AB - 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-HT 1BR), 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-HT 1BR activity, whose inhibition promotes an anxiogenic behavioural response. Collectively, our data unveil a new facet of PrPC signalling that strengthens neurotransmission.
U2 - 10.1038/srep04881
DO - 10.1038/srep04881
M3 - Article
C2 - 24810941
AN - SCOPUS:84905507339
SN - 2045-2322
VL - 4
JO - Scientific Reports
JF - Scientific Reports
M1 - 4881
ER -