TY - JOUR
T1 - The fibroblast growth factor 14·voltage-gated sodium channel complex is a new target of glycogen synthase kinase 3 (GSK3)
AU - Shavkunov, Alexander S.
AU - Wildburger, Norelle C.
AU - Nenov, Miroslav
AU - James, Thomas F.
AU - Buzhdygan, Tetyana
AU - Panova-Elektronova, Neli I.
AU - Green, Thomas A.
AU - Veselenak, Ronald L.
AU - Bourne, Nigel
AU - Laezza, Fernanda
PY - 2013/7/5
Y1 - 2013/7/5
N2 - The FGF14 protein controls biophysical properties and subcellular distribution of neuronal voltage-gated Na+ (Nav) channels through direct binding to the channel C terminus. To gain insights into the dynamic regulation of this protein/protein interaction complex, we employed the split luciferase complementation assay to screen a small molecule library of kinase inhibitors against the FGF14·Nav1.6 channel complex and identified inhibitors of GSK3 as hits. Through a combination of a luminescence-based counter-screening, co-immunoprecipitation, patch clamp electrophysiology, and quantitative confocal immunofluorescence, we demonstrate that inhibition of GSK3 reduces the assembly of the FGF14·Nav channel complex, modifies FGF14- dependent regulation of Na+ currents, and induces dissociation and subcellular redistribution of the native FGF14·Nav channel complex in hippocampal neurons. These results further emphasize the role of FGF14 as a critical component of the Nav channel macromolecular complex, providing evidence for a novelGSK3-dependent signaling pathway that might control excitability through specific protein/protein interactions.
AB - The FGF14 protein controls biophysical properties and subcellular distribution of neuronal voltage-gated Na+ (Nav) channels through direct binding to the channel C terminus. To gain insights into the dynamic regulation of this protein/protein interaction complex, we employed the split luciferase complementation assay to screen a small molecule library of kinase inhibitors against the FGF14·Nav1.6 channel complex and identified inhibitors of GSK3 as hits. Through a combination of a luminescence-based counter-screening, co-immunoprecipitation, patch clamp electrophysiology, and quantitative confocal immunofluorescence, we demonstrate that inhibition of GSK3 reduces the assembly of the FGF14·Nav channel complex, modifies FGF14- dependent regulation of Na+ currents, and induces dissociation and subcellular redistribution of the native FGF14·Nav channel complex in hippocampal neurons. These results further emphasize the role of FGF14 as a critical component of the Nav channel macromolecular complex, providing evidence for a novelGSK3-dependent signaling pathway that might control excitability through specific protein/protein interactions.
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U2 - 10.1074/jbc.M112.445924
DO - 10.1074/jbc.M112.445924
M3 - Article
C2 - 23640885
AN - SCOPUS:84880055131
SN - 0021-9258
VL - 288
SP - 19370
EP - 19385
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 27
ER -