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SAP97 and CASK mediate sorting of N-Methyl-D-Aspartate Receptors through a novel secretory pathway

Synaptic plasticity is dependent upon the differential sorting, delivery and retention of neurotransmitter receptors, yet the mechanisms underlying these processes are poorly understood. In the present study, we have found that differential sorting of glutamate receptor subtypes begins within the en...

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Detalles Bibliográficos
Autores principales: Jeyifous, Okunola, Waites, Clarissa L., Specht, Christian G., Fujisawa, Sho, Schubert, Manja, Lin, Eric, Marshall, John, Aoki, Chiye, de Silva, Tharani, Montgomery, Johanna M., Garner, Craig C., Green, William N.
Formato: Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779056/
https://www.ncbi.nlm.nih.gov/pubmed/19620977
http://dx.doi.org/10.1038/nn.2362
Descripción
Sumario:Synaptic plasticity is dependent upon the differential sorting, delivery and retention of neurotransmitter receptors, yet the mechanisms underlying these processes are poorly understood. In the present study, we have found that differential sorting of glutamate receptor subtypes begins within the endoplasmic reticulum (ER) of rat hippocampal neurons. While AMPARs are trafficked to the plasma membrane via the conventional somatic Golgi network, NMDARs are diverted from the somatic ER into a specialized ER sub-compartment that bypasses somatic Golgi, merging instead with dendritic Golgi outposts. Intriguingly, this ER sub-compartment is composed of highly mobile vesicles containing the NMDAR subunits NR1 and NR2B, the microtubule-dependent motor protein KIF17, and the postsynaptic adaptor proteins CASK and SAP97. Furthermore, our data demonstrate that the retention and trafficking of NMDARs within this ER sub-compartment requires both CASK and SAP97. These data indicate that NMDARs are sorted away from AMPARs via a non-conventional secretory pathway that utilizes dendritic Golgi outposts.