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Zinc transporter-1 concentrates at the postsynaptic density of hippocampal synapses
BACKGROUND: Zinc concentrates at excitatory synapses, both at the postsynaptic density and in a subset of glutamatergic boutons. Zinc can modulate synaptic plasticity, memory formation and nociception by regulating transmitter receptors and signal transduction pathways. Also, intracellular zinc accu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975337/ https://www.ncbi.nlm.nih.gov/pubmed/24602382 http://dx.doi.org/10.1186/1756-6606-7-16 |
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author | Sindreu, Carlos Bayés, Àlex Altafaj, Xavier Pérez-Clausell, Jeús |
author_facet | Sindreu, Carlos Bayés, Àlex Altafaj, Xavier Pérez-Clausell, Jeús |
author_sort | Sindreu, Carlos |
collection | PubMed |
description | BACKGROUND: Zinc concentrates at excitatory synapses, both at the postsynaptic density and in a subset of glutamatergic boutons. Zinc can modulate synaptic plasticity, memory formation and nociception by regulating transmitter receptors and signal transduction pathways. Also, intracellular zinc accumulation is a hallmark of degenerating neurons in several neurological disorders. To date, no single zinc extrusion mechanism has been directly localized to synapses. Based on the presence of a canonical PDZ I motif in the Zinc Transporter-1 protein (ZnT1), we hypothesized that ZnT1 may be targeted to synaptic compartments for local control of cytosolic zinc. Using our previously developed protocol for the co-localization of reactive zinc and synaptic proteins, we further asked if ZnT1 expression correlates with presynaptic zinc content in individual synapses. FINDINGS: Here we demonstrate that ZnT1 is a plasma membrane protein that is enriched in dendritic spines and in biochemically isolated synaptic membranes. Hippocampal CA1 synapses labelled by postembedding immunogold showed over a 5-fold increase in ZnT1 concentration at synaptic junctions compared with extrasynaptic membranes. Subsynaptic analysis revealed a peak ZnT1 density on the postsynaptic side of the synapse, < 10 nm away from the postsynaptic membrane. ZnT1 was found in the vast majority of excitatory synapses regardless of the presence of vesicular zinc in presynaptic boutons. CONCLUSIONS: Our study has identified ZnT1 as a novel postsynaptic density protein, and it may help elucidate the role of zinc homeostasis in synaptic function and disease. |
format | Online Article Text |
id | pubmed-3975337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39753372014-04-05 Zinc transporter-1 concentrates at the postsynaptic density of hippocampal synapses Sindreu, Carlos Bayés, Àlex Altafaj, Xavier Pérez-Clausell, Jeús Mol Brain Short Report BACKGROUND: Zinc concentrates at excitatory synapses, both at the postsynaptic density and in a subset of glutamatergic boutons. Zinc can modulate synaptic plasticity, memory formation and nociception by regulating transmitter receptors and signal transduction pathways. Also, intracellular zinc accumulation is a hallmark of degenerating neurons in several neurological disorders. To date, no single zinc extrusion mechanism has been directly localized to synapses. Based on the presence of a canonical PDZ I motif in the Zinc Transporter-1 protein (ZnT1), we hypothesized that ZnT1 may be targeted to synaptic compartments for local control of cytosolic zinc. Using our previously developed protocol for the co-localization of reactive zinc and synaptic proteins, we further asked if ZnT1 expression correlates with presynaptic zinc content in individual synapses. FINDINGS: Here we demonstrate that ZnT1 is a plasma membrane protein that is enriched in dendritic spines and in biochemically isolated synaptic membranes. Hippocampal CA1 synapses labelled by postembedding immunogold showed over a 5-fold increase in ZnT1 concentration at synaptic junctions compared with extrasynaptic membranes. Subsynaptic analysis revealed a peak ZnT1 density on the postsynaptic side of the synapse, < 10 nm away from the postsynaptic membrane. ZnT1 was found in the vast majority of excitatory synapses regardless of the presence of vesicular zinc in presynaptic boutons. CONCLUSIONS: Our study has identified ZnT1 as a novel postsynaptic density protein, and it may help elucidate the role of zinc homeostasis in synaptic function and disease. BioMed Central 2014-03-07 /pmc/articles/PMC3975337/ /pubmed/24602382 http://dx.doi.org/10.1186/1756-6606-7-16 Text en Copyright © 2014 Sindreu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Sindreu, Carlos Bayés, Àlex Altafaj, Xavier Pérez-Clausell, Jeús Zinc transporter-1 concentrates at the postsynaptic density of hippocampal synapses |
title | Zinc transporter-1 concentrates at the postsynaptic density of hippocampal synapses |
title_full | Zinc transporter-1 concentrates at the postsynaptic density of hippocampal synapses |
title_fullStr | Zinc transporter-1 concentrates at the postsynaptic density of hippocampal synapses |
title_full_unstemmed | Zinc transporter-1 concentrates at the postsynaptic density of hippocampal synapses |
title_short | Zinc transporter-1 concentrates at the postsynaptic density of hippocampal synapses |
title_sort | zinc transporter-1 concentrates at the postsynaptic density of hippocampal synapses |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975337/ https://www.ncbi.nlm.nih.gov/pubmed/24602382 http://dx.doi.org/10.1186/1756-6606-7-16 |
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