Identification of a novel signaling pathway and its relevance for GluA1 recycling.

We previously showed that the serum- and glucocorticoid-inducible kinase 3 (SGK3) increases the AMPA-type glutamate receptor GluA1 protein in the plasma membrane. The activation of AMPA receptors by NMDA-type glutamate receptors eventually leads to postsynaptic neuronal plasticity. Here, we show tha...

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Main Authors: Guiscard Seebohm, Sebastian Neumann, Carsten Theiss, Tanja Novkovic, Elaine V Hill, Jeremy M Tavaré, Florian Lang, Michael Hollmann, Denise Manahan-Vaughan, Nathalie Strutz-Seebohm
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0033889&type=printable
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author Guiscard Seebohm
Sebastian Neumann
Carsten Theiss
Tanja Novkovic
Elaine V Hill
Jeremy M Tavaré
Florian Lang
Michael Hollmann
Denise Manahan-Vaughan
Nathalie Strutz-Seebohm
author_facet Guiscard Seebohm
Sebastian Neumann
Carsten Theiss
Tanja Novkovic
Elaine V Hill
Jeremy M Tavaré
Florian Lang
Michael Hollmann
Denise Manahan-Vaughan
Nathalie Strutz-Seebohm
author_sort Guiscard Seebohm
collection DOAJ
description We previously showed that the serum- and glucocorticoid-inducible kinase 3 (SGK3) increases the AMPA-type glutamate receptor GluA1 protein in the plasma membrane. The activation of AMPA receptors by NMDA-type glutamate receptors eventually leads to postsynaptic neuronal plasticity. Here, we show that SGK3 mRNA is upregulated in the hippocampus of new-born wild type Wistar rats after NMDA receptor activation. We further demonstrate in the Xenopus oocyte expression system that delivery of GluA1 protein to the plasma membrane depends on the small GTPase RAB11. This RAB-dependent GluA1 trafficking requires phosphorylation and activation of phosphoinositol-3-phosphate-5-kinase (PIKfyve) and the generation of PI(3,5)P(2). In line with this mechanism we could show PIKfyve mRNA expression in the hippocampus of wild type C57/BL6 mice and phosphorylation of PIKfyve by SGK3. Incubation of hippocampal slices with the PIKfyve inhibitor YM201636 revealed reduced CA1 basal synaptic activity. Furthermore, treatment of primary hippocampal neurons with YM201636 altered the GluA1 expression pattern towards reduced synaptic expression of GluA1. Our findings demonstrate for the first time an involvement of PIKfyve and PI(3,5)P(2) in NMDA receptor-triggered synaptic GluA1 trafficking. This new regulatory pathway of GluA1 may contribute to synaptic plasticity and memory.
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spelling doaj-art-53d30c51b7ab4e8c8dafc959c34a8f752025-08-20T03:09:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0173e3388910.1371/journal.pone.0033889Identification of a novel signaling pathway and its relevance for GluA1 recycling.Guiscard SeebohmSebastian NeumannCarsten TheissTanja NovkovicElaine V HillJeremy M TavaréFlorian LangMichael HollmannDenise Manahan-VaughanNathalie Strutz-SeebohmWe previously showed that the serum- and glucocorticoid-inducible kinase 3 (SGK3) increases the AMPA-type glutamate receptor GluA1 protein in the plasma membrane. The activation of AMPA receptors by NMDA-type glutamate receptors eventually leads to postsynaptic neuronal plasticity. Here, we show that SGK3 mRNA is upregulated in the hippocampus of new-born wild type Wistar rats after NMDA receptor activation. We further demonstrate in the Xenopus oocyte expression system that delivery of GluA1 protein to the plasma membrane depends on the small GTPase RAB11. This RAB-dependent GluA1 trafficking requires phosphorylation and activation of phosphoinositol-3-phosphate-5-kinase (PIKfyve) and the generation of PI(3,5)P(2). In line with this mechanism we could show PIKfyve mRNA expression in the hippocampus of wild type C57/BL6 mice and phosphorylation of PIKfyve by SGK3. Incubation of hippocampal slices with the PIKfyve inhibitor YM201636 revealed reduced CA1 basal synaptic activity. Furthermore, treatment of primary hippocampal neurons with YM201636 altered the GluA1 expression pattern towards reduced synaptic expression of GluA1. Our findings demonstrate for the first time an involvement of PIKfyve and PI(3,5)P(2) in NMDA receptor-triggered synaptic GluA1 trafficking. This new regulatory pathway of GluA1 may contribute to synaptic plasticity and memory.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0033889&type=printable
spellingShingle Guiscard Seebohm
Sebastian Neumann
Carsten Theiss
Tanja Novkovic
Elaine V Hill
Jeremy M Tavaré
Florian Lang
Michael Hollmann
Denise Manahan-Vaughan
Nathalie Strutz-Seebohm
Identification of a novel signaling pathway and its relevance for GluA1 recycling.
PLoS ONE
title Identification of a novel signaling pathway and its relevance for GluA1 recycling.
title_full Identification of a novel signaling pathway and its relevance for GluA1 recycling.
title_fullStr Identification of a novel signaling pathway and its relevance for GluA1 recycling.
title_full_unstemmed Identification of a novel signaling pathway and its relevance for GluA1 recycling.
title_short Identification of a novel signaling pathway and its relevance for GluA1 recycling.
title_sort identification of a novel signaling pathway and its relevance for glua1 recycling
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0033889&type=printable
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