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Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus
Members of the Shank family of multidomain proteins (Shank1, Shank2, and Shank3) are core components of the postsynaptic density (PSD) of excitatory synapses. At synaptic sites Shanks serve as scaffolding molecules that cluster neurotransmitter receptors as well as cell adhesion molecules attaching...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844616/ https://www.ncbi.nlm.nih.gov/pubmed/27199660 http://dx.doi.org/10.3389/fncel.2016.00106 |
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author | Heise, Christopher Schroeder, Jan C. Schoen, Michael Halbedl, Sonja Reim, Dominik Woelfle, Sarah Kreutz, Michael R. Schmeisser, Michael J. Boeckers, Tobias M. |
author_facet | Heise, Christopher Schroeder, Jan C. Schoen, Michael Halbedl, Sonja Reim, Dominik Woelfle, Sarah Kreutz, Michael R. Schmeisser, Michael J. Boeckers, Tobias M. |
author_sort | Heise, Christopher |
collection | PubMed |
description | Members of the Shank family of multidomain proteins (Shank1, Shank2, and Shank3) are core components of the postsynaptic density (PSD) of excitatory synapses. At synaptic sites Shanks serve as scaffolding molecules that cluster neurotransmitter receptors as well as cell adhesion molecules attaching them to the actin cytoskeleton. In this study we investigated the synapse specific localization of Shank1-3 and focused on well-defined synaptic contacts within the hippocampal formation. We found that all three family members are present only at VGLUT1-positive synapses, which is particularly visible at mossy fiber contacts. No costaining was found at VGLUT2-positive contacts indicating that the molecular organization of VGLUT2-associated PSDs diverges from classical VGLUT1-positive excitatory contacts in the hippocampus. In light of SHANK mutations in neuropsychiatric disorders, this study indicates which glutamatergic networks within the hippocampus will be primarily affected by shankopathies. |
format | Online Article Text |
id | pubmed-4844616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48446162016-05-19 Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus Heise, Christopher Schroeder, Jan C. Schoen, Michael Halbedl, Sonja Reim, Dominik Woelfle, Sarah Kreutz, Michael R. Schmeisser, Michael J. Boeckers, Tobias M. Front Cell Neurosci Neuroscience Members of the Shank family of multidomain proteins (Shank1, Shank2, and Shank3) are core components of the postsynaptic density (PSD) of excitatory synapses. At synaptic sites Shanks serve as scaffolding molecules that cluster neurotransmitter receptors as well as cell adhesion molecules attaching them to the actin cytoskeleton. In this study we investigated the synapse specific localization of Shank1-3 and focused on well-defined synaptic contacts within the hippocampal formation. We found that all three family members are present only at VGLUT1-positive synapses, which is particularly visible at mossy fiber contacts. No costaining was found at VGLUT2-positive contacts indicating that the molecular organization of VGLUT2-associated PSDs diverges from classical VGLUT1-positive excitatory contacts in the hippocampus. In light of SHANK mutations in neuropsychiatric disorders, this study indicates which glutamatergic networks within the hippocampus will be primarily affected by shankopathies. Frontiers Media S.A. 2016-04-26 /pmc/articles/PMC4844616/ /pubmed/27199660 http://dx.doi.org/10.3389/fncel.2016.00106 Text en Copyright © 2016 Heise, Schroeder, Schoen, Halbedl, Reim, Woelfle, Kreutz, Schmeisser and Boeckers. 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 Heise, Christopher Schroeder, Jan C. Schoen, Michael Halbedl, Sonja Reim, Dominik Woelfle, Sarah Kreutz, Michael R. Schmeisser, Michael J. Boeckers, Tobias M. Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus |
title | Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus |
title_full | Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus |
title_fullStr | Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus |
title_full_unstemmed | Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus |
title_short | Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus |
title_sort | selective localization of shanks to vglut1-positive excitatory synapses in the mouse hippocampus |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844616/ https://www.ncbi.nlm.nih.gov/pubmed/27199660 http://dx.doi.org/10.3389/fncel.2016.00106 |
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