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Ultrastructural heterogeneity of layer 4 excitatory synaptic boutons in the adult human temporal lobe neocortex
Synapses are fundamental building blocks controlling and modulating the ‘behavior’ of brain networks. How their structural composition, most notably their quantitative morphology underlie their computational properties remains rather unclear, particularly in humans. Here, excitatory synaptic boutons...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6919978/ https://www.ncbi.nlm.nih.gov/pubmed/31746736 http://dx.doi.org/10.7554/eLife.48373 |
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author | Yakoubi, Rachida Rollenhagen, Astrid von Lehe, Marec Miller, Dorothea Walkenfort, Bernd Hasenberg, Mike Sätzler, Kurt Lübke, Joachim HR |
author_facet | Yakoubi, Rachida Rollenhagen, Astrid von Lehe, Marec Miller, Dorothea Walkenfort, Bernd Hasenberg, Mike Sätzler, Kurt Lübke, Joachim HR |
author_sort | Yakoubi, Rachida |
collection | PubMed |
description | Synapses are fundamental building blocks controlling and modulating the ‘behavior’ of brain networks. How their structural composition, most notably their quantitative morphology underlie their computational properties remains rather unclear, particularly in humans. Here, excitatory synaptic boutons (SBs) in layer 4 (L4) of the temporal lobe neocortex (TLN) were quantitatively investigated. Biopsies from epilepsy surgery were used for fine-scale and tomographic electron microscopy (EM) to generate 3D-reconstructions of SBs. Particularly, the size of active zones (AZs) and that of the three functionally defined pools of synaptic vesicles (SVs) were quantified. SBs were comparatively small (~2.50 μm(2)), with a single AZ (~0.13 µm(2)); preferentially established on spines. SBs had a total pool of ~1800 SVs with strikingly large readily releasable (~20), recycling (~80) and resting pools (~850). Thus, human L4 SBs may act as ‘amplifiers’ of signals from the sensory periphery, integrate, synchronize and modulate intra- and extracortical synaptic activity. |
format | Online Article Text |
id | pubmed-6919978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69199782019-12-19 Ultrastructural heterogeneity of layer 4 excitatory synaptic boutons in the adult human temporal lobe neocortex Yakoubi, Rachida Rollenhagen, Astrid von Lehe, Marec Miller, Dorothea Walkenfort, Bernd Hasenberg, Mike Sätzler, Kurt Lübke, Joachim HR eLife Neuroscience Synapses are fundamental building blocks controlling and modulating the ‘behavior’ of brain networks. How their structural composition, most notably their quantitative morphology underlie their computational properties remains rather unclear, particularly in humans. Here, excitatory synaptic boutons (SBs) in layer 4 (L4) of the temporal lobe neocortex (TLN) were quantitatively investigated. Biopsies from epilepsy surgery were used for fine-scale and tomographic electron microscopy (EM) to generate 3D-reconstructions of SBs. Particularly, the size of active zones (AZs) and that of the three functionally defined pools of synaptic vesicles (SVs) were quantified. SBs were comparatively small (~2.50 μm(2)), with a single AZ (~0.13 µm(2)); preferentially established on spines. SBs had a total pool of ~1800 SVs with strikingly large readily releasable (~20), recycling (~80) and resting pools (~850). Thus, human L4 SBs may act as ‘amplifiers’ of signals from the sensory periphery, integrate, synchronize and modulate intra- and extracortical synaptic activity. eLife Sciences Publications, Ltd 2019-11-20 /pmc/articles/PMC6919978/ /pubmed/31746736 http://dx.doi.org/10.7554/eLife.48373 Text en © 2019, Yakoubi et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Yakoubi, Rachida Rollenhagen, Astrid von Lehe, Marec Miller, Dorothea Walkenfort, Bernd Hasenberg, Mike Sätzler, Kurt Lübke, Joachim HR Ultrastructural heterogeneity of layer 4 excitatory synaptic boutons in the adult human temporal lobe neocortex |
title | Ultrastructural heterogeneity of layer 4 excitatory synaptic boutons in the adult human temporal lobe neocortex |
title_full | Ultrastructural heterogeneity of layer 4 excitatory synaptic boutons in the adult human temporal lobe neocortex |
title_fullStr | Ultrastructural heterogeneity of layer 4 excitatory synaptic boutons in the adult human temporal lobe neocortex |
title_full_unstemmed | Ultrastructural heterogeneity of layer 4 excitatory synaptic boutons in the adult human temporal lobe neocortex |
title_short | Ultrastructural heterogeneity of layer 4 excitatory synaptic boutons in the adult human temporal lobe neocortex |
title_sort | ultrastructural heterogeneity of layer 4 excitatory synaptic boutons in the adult human temporal lobe neocortex |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6919978/ https://www.ncbi.nlm.nih.gov/pubmed/31746736 http://dx.doi.org/10.7554/eLife.48373 |
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