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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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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
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author 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.
author_facet 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.
author_sort Jeyifous, Okunola
collection PubMed
description 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.
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spelling pubmed-27790562010-02-01 SAP97 and CASK mediate sorting of N-Methyl-D-Aspartate Receptors through a novel secretory pathway 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. Nat Neurosci Article 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. 2009-07-20 2009-08 /pmc/articles/PMC2779056/ /pubmed/19620977 http://dx.doi.org/10.1038/nn.2362 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
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.
SAP97 and CASK mediate sorting of N-Methyl-D-Aspartate Receptors through a novel secretory pathway
title SAP97 and CASK mediate sorting of N-Methyl-D-Aspartate Receptors through a novel secretory pathway
title_full SAP97 and CASK mediate sorting of N-Methyl-D-Aspartate Receptors through a novel secretory pathway
title_fullStr SAP97 and CASK mediate sorting of N-Methyl-D-Aspartate Receptors through a novel secretory pathway
title_full_unstemmed SAP97 and CASK mediate sorting of N-Methyl-D-Aspartate Receptors through a novel secretory pathway
title_short SAP97 and CASK mediate sorting of N-Methyl-D-Aspartate Receptors through a novel secretory pathway
title_sort sap97 and cask mediate sorting of n-methyl-d-aspartate receptors through a novel secretory pathway
topic Article
url 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
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