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GluN2D-containing NMDA receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice

The differential regulation of the two major N-methyl-D-aspartate receptor (NMDAR) subunits GluN2A and GluN2B during development in forebrain pyramidal cells has been thoroughly investigated. In contrast, much less is known about the role of GluN2D, which is expressed at low levels and is downregula...

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Autores principales: von Engelhardt, Jakob, Bocklisch, Christina, Tönges, Lars, Herb, Anne, Mishina, Masayoshi, Monyer, Hannah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373385/
https://www.ncbi.nlm.nih.gov/pubmed/25859181
http://dx.doi.org/10.3389/fncel.2015.00095
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author von Engelhardt, Jakob
Bocklisch, Christina
Tönges, Lars
Herb, Anne
Mishina, Masayoshi
Monyer, Hannah
author_facet von Engelhardt, Jakob
Bocklisch, Christina
Tönges, Lars
Herb, Anne
Mishina, Masayoshi
Monyer, Hannah
author_sort von Engelhardt, Jakob
collection PubMed
description The differential regulation of the two major N-methyl-D-aspartate receptor (NMDAR) subunits GluN2A and GluN2B during development in forebrain pyramidal cells has been thoroughly investigated. In contrast, much less is known about the role of GluN2D, which is expressed at low levels and is downregulated following the second postnatal week. However, it appears that few cells, presumably interneurons, continue to express GluN2D also in juvenile mice. To investigate which hippocampal cell types express this subunit, we generated transgenic mice with EGFP-tagged GluN2D receptors. The expression of the transgene was confined to hippocampal interneurons, most of which were parvalbumin- and/or somatostatin-positive. Electrophysiological and morphological analyses showed that GluN2D was present mainly in fast spiking basket and axo-axonic cells. Based on pharmacological evidence and electrophysiological analysis of GluN2D knockout mice, we conclude that GluN2D-containing NMDARs mediate synaptic currents in hippocampal interneurons of young and juvenile mice and in CA1 pyramidal neurons of newborn mice.
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spelling pubmed-43733852015-04-09 GluN2D-containing NMDA receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice von Engelhardt, Jakob Bocklisch, Christina Tönges, Lars Herb, Anne Mishina, Masayoshi Monyer, Hannah Front Cell Neurosci Neuroscience The differential regulation of the two major N-methyl-D-aspartate receptor (NMDAR) subunits GluN2A and GluN2B during development in forebrain pyramidal cells has been thoroughly investigated. In contrast, much less is known about the role of GluN2D, which is expressed at low levels and is downregulated following the second postnatal week. However, it appears that few cells, presumably interneurons, continue to express GluN2D also in juvenile mice. To investigate which hippocampal cell types express this subunit, we generated transgenic mice with EGFP-tagged GluN2D receptors. The expression of the transgene was confined to hippocampal interneurons, most of which were parvalbumin- and/or somatostatin-positive. Electrophysiological and morphological analyses showed that GluN2D was present mainly in fast spiking basket and axo-axonic cells. Based on pharmacological evidence and electrophysiological analysis of GluN2D knockout mice, we conclude that GluN2D-containing NMDARs mediate synaptic currents in hippocampal interneurons of young and juvenile mice and in CA1 pyramidal neurons of newborn mice. Frontiers Media S.A. 2015-03-25 /pmc/articles/PMC4373385/ /pubmed/25859181 http://dx.doi.org/10.3389/fncel.2015.00095 Text en Copyright © 2015 von Engelhardt, Bocklisch, Tönges, Herb, Mishina and Monyer. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
von Engelhardt, Jakob
Bocklisch, Christina
Tönges, Lars
Herb, Anne
Mishina, Masayoshi
Monyer, Hannah
GluN2D-containing NMDA receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice
title GluN2D-containing NMDA receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice
title_full GluN2D-containing NMDA receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice
title_fullStr GluN2D-containing NMDA receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice
title_full_unstemmed GluN2D-containing NMDA receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice
title_short GluN2D-containing NMDA receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice
title_sort glun2d-containing nmda receptors-mediate synaptic currents in hippocampal interneurons and pyramidal cells in juvenile mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373385/
https://www.ncbi.nlm.nih.gov/pubmed/25859181
http://dx.doi.org/10.3389/fncel.2015.00095
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