Cargando…
Area-Specific Synapse Structure in Branched Posterior Nucleus Axons Reveals a New Level of Complexity in Thalamocortical Networks
Thalamocortical posterior nucleus (Po) axons innervating the vibrissal somatosensory (S1) and motor (MC) cortices are key links in the brain neuronal network that allows rodents to explore the environment whisking with their motile snout vibrissae. Here, using fine-scale high-end 3D electron microsc...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096142/ https://www.ncbi.nlm.nih.gov/pubmed/32054677 http://dx.doi.org/10.1523/JNEUROSCI.2886-19.2020 |
_version_ | 1783510759234338816 |
---|---|
author | Rodriguez-Moreno, Javier Porrero, Cesar Rollenhagen, Astrid Rubio-Teves, Mario Casas-Torremocha, Diana Alonso-Nanclares, Lidia Yakoubi, Rachida Santuy, Andrea Merchan-Pérez, Angel DeFelipe, Javier Lübke, Joachim H.R. Clasca, Francisco |
author_facet | Rodriguez-Moreno, Javier Porrero, Cesar Rollenhagen, Astrid Rubio-Teves, Mario Casas-Torremocha, Diana Alonso-Nanclares, Lidia Yakoubi, Rachida Santuy, Andrea Merchan-Pérez, Angel DeFelipe, Javier Lübke, Joachim H.R. Clasca, Francisco |
author_sort | Rodriguez-Moreno, Javier |
collection | PubMed |
description | Thalamocortical posterior nucleus (Po) axons innervating the vibrissal somatosensory (S1) and motor (MC) cortices are key links in the brain neuronal network that allows rodents to explore the environment whisking with their motile snout vibrissae. Here, using fine-scale high-end 3D electron microscopy, we demonstrate in adult male C57BL/6 wild-type mice marked differences between MC versus S1 Po synapses in (1) bouton and active zone size, (2) neurotransmitter vesicle pool size, (3) distribution of mitochondria around synapses, and (4) proportion of synapses established on dendritic spines and dendritic shafts. These differences are as large, or even more pronounced, than those between Po and ventro-posterior thalamic nucleus synapses in S1. Moreover, using single-axon transfection labeling, we demonstrate that the above differences actually occur on the MC versus the S1 branches of individual Po cell axons that innervate both areas. Along with recently-discovered divergences in efficacy and plasticity, the synaptic structure differences reported here thus reveal a new subcellular level of complexity. This is a finding that upends current models of thalamocortical circuitry, and that might as well illuminate the functional logic of other branched projection axon systems. SIGNIFICANCE STATEMENT Many long-distance brain connections depend on neurons whose branched axons target separate regions. Using 3D electron microscopy and single-cell transfection, we investigated the mouse Posterior thalamic nucleus (Po) cell axons that simultaneously innervate motor and sensory areas of the cerebral cortex involved in whisker movement control. We demonstrate significant differences in the size of the boutons made in each area by individual Po axons, as well as in functionally-relevant parameters in the composition of their synapses. In addition, we found similarly large differences between the synapses of Po versus ventral posteromedial thalamic nucleus axons in the whisker sensory cortex. Area-specific synapse structure in individual axons implies a new, unsuspected level of complexity in long-distance brain connections. |
format | Online Article Text |
id | pubmed-7096142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-70961422020-03-26 Area-Specific Synapse Structure in Branched Posterior Nucleus Axons Reveals a New Level of Complexity in Thalamocortical Networks Rodriguez-Moreno, Javier Porrero, Cesar Rollenhagen, Astrid Rubio-Teves, Mario Casas-Torremocha, Diana Alonso-Nanclares, Lidia Yakoubi, Rachida Santuy, Andrea Merchan-Pérez, Angel DeFelipe, Javier Lübke, Joachim H.R. Clasca, Francisco J Neurosci Research Articles Thalamocortical posterior nucleus (Po) axons innervating the vibrissal somatosensory (S1) and motor (MC) cortices are key links in the brain neuronal network that allows rodents to explore the environment whisking with their motile snout vibrissae. Here, using fine-scale high-end 3D electron microscopy, we demonstrate in adult male C57BL/6 wild-type mice marked differences between MC versus S1 Po synapses in (1) bouton and active zone size, (2) neurotransmitter vesicle pool size, (3) distribution of mitochondria around synapses, and (4) proportion of synapses established on dendritic spines and dendritic shafts. These differences are as large, or even more pronounced, than those between Po and ventro-posterior thalamic nucleus synapses in S1. Moreover, using single-axon transfection labeling, we demonstrate that the above differences actually occur on the MC versus the S1 branches of individual Po cell axons that innervate both areas. Along with recently-discovered divergences in efficacy and plasticity, the synaptic structure differences reported here thus reveal a new subcellular level of complexity. This is a finding that upends current models of thalamocortical circuitry, and that might as well illuminate the functional logic of other branched projection axon systems. SIGNIFICANCE STATEMENT Many long-distance brain connections depend on neurons whose branched axons target separate regions. Using 3D electron microscopy and single-cell transfection, we investigated the mouse Posterior thalamic nucleus (Po) cell axons that simultaneously innervate motor and sensory areas of the cerebral cortex involved in whisker movement control. We demonstrate significant differences in the size of the boutons made in each area by individual Po axons, as well as in functionally-relevant parameters in the composition of their synapses. In addition, we found similarly large differences between the synapses of Po versus ventral posteromedial thalamic nucleus axons in the whisker sensory cortex. Area-specific synapse structure in individual axons implies a new, unsuspected level of complexity in long-distance brain connections. Society for Neuroscience 2020-03-25 /pmc/articles/PMC7096142/ /pubmed/32054677 http://dx.doi.org/10.1523/JNEUROSCI.2886-19.2020 Text en Copyright © 2020 Rodriguez-Moreno et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License Creative Commons Attribution 4.0 International (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Articles Rodriguez-Moreno, Javier Porrero, Cesar Rollenhagen, Astrid Rubio-Teves, Mario Casas-Torremocha, Diana Alonso-Nanclares, Lidia Yakoubi, Rachida Santuy, Andrea Merchan-Pérez, Angel DeFelipe, Javier Lübke, Joachim H.R. Clasca, Francisco Area-Specific Synapse Structure in Branched Posterior Nucleus Axons Reveals a New Level of Complexity in Thalamocortical Networks |
title | Area-Specific Synapse Structure in Branched Posterior Nucleus Axons Reveals a New Level of Complexity in Thalamocortical Networks |
title_full | Area-Specific Synapse Structure in Branched Posterior Nucleus Axons Reveals a New Level of Complexity in Thalamocortical Networks |
title_fullStr | Area-Specific Synapse Structure in Branched Posterior Nucleus Axons Reveals a New Level of Complexity in Thalamocortical Networks |
title_full_unstemmed | Area-Specific Synapse Structure in Branched Posterior Nucleus Axons Reveals a New Level of Complexity in Thalamocortical Networks |
title_short | Area-Specific Synapse Structure in Branched Posterior Nucleus Axons Reveals a New Level of Complexity in Thalamocortical Networks |
title_sort | area-specific synapse structure in branched posterior nucleus axons reveals a new level of complexity in thalamocortical networks |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096142/ https://www.ncbi.nlm.nih.gov/pubmed/32054677 http://dx.doi.org/10.1523/JNEUROSCI.2886-19.2020 |
work_keys_str_mv | AT rodriguezmorenojavier areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks AT porrerocesar areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks AT rollenhagenastrid areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks AT rubiotevesmario areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks AT casastorremochadiana areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks AT alonsonanclareslidia areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks AT yakoubirachida areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks AT santuyandrea areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks AT merchanperezangel areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks AT defelipejavier areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks AT lubkejoachimhr areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks AT clascafrancisco areaspecificsynapsestructureinbranchedposteriornucleusaxonsrevealsanewlevelofcomplexityinthalamocorticalnetworks |