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Pioneer glutamatergic cells develop into a morpho-functionally distinct population in the juvenile CA3 hippocampus

The developing CA3 hippocampus is comprised by highly connected hub neurons that are particularly effective in achieving network synchronization. Functional hub neurons were shown to be exclusively GABAergic, suggesting that the contribution of glutamatergic neurons to physiological synchronization...

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Autores principales: Marissal, Thomas, Bonifazi, Paolo, Picardo, Michel Aimé, Nardou, Romain, Petit, Ludovic Franck, Baude, Agnès, Fishell, Gordon James, Ben-Ari, Yehezkel, Cossart, Rosa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3535425/
https://www.ncbi.nlm.nih.gov/pubmed/23271650
http://dx.doi.org/10.1038/ncomms2318
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author Marissal, Thomas
Bonifazi, Paolo
Picardo, Michel Aimé
Nardou, Romain
Petit, Ludovic Franck
Baude, Agnès
Fishell, Gordon James
Ben-Ari, Yehezkel
Cossart, Rosa
author_facet Marissal, Thomas
Bonifazi, Paolo
Picardo, Michel Aimé
Nardou, Romain
Petit, Ludovic Franck
Baude, Agnès
Fishell, Gordon James
Ben-Ari, Yehezkel
Cossart, Rosa
author_sort Marissal, Thomas
collection PubMed
description The developing CA3 hippocampus is comprised by highly connected hub neurons that are particularly effective in achieving network synchronization. Functional hub neurons were shown to be exclusively GABAergic, suggesting that the contribution of glutamatergic neurons to physiological synchronization processes at early postnatal stages is minimal. However, without fast GABAergic transmission, a different situation may prevail. In the adult CA3, blocking fast GABAergic transmission induces the generation of network bursts that can be triggered by the stimulation of single pyramidal neurons. Here we revisit the network function of CA3 glutamatergic neurons from a developmental viewpoint, without fast GABAergic transmission. We uncover a sub-population of early-generated glutamatergic neurons that impacts network dynamics when stimulated in the juvenile hippocampus. Additionally, this population displays characteristic morpho-physiological features in the juvenile and adult hippocampus. Therefore, the apparently homogeneous glutamatergic cell population likely displays a morpho-functional diversity rooted in temporal embryonic origins.
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spelling pubmed-35354252013-01-03 Pioneer glutamatergic cells develop into a morpho-functionally distinct population in the juvenile CA3 hippocampus Marissal, Thomas Bonifazi, Paolo Picardo, Michel Aimé Nardou, Romain Petit, Ludovic Franck Baude, Agnès Fishell, Gordon James Ben-Ari, Yehezkel Cossart, Rosa Nat Commun Article The developing CA3 hippocampus is comprised by highly connected hub neurons that are particularly effective in achieving network synchronization. Functional hub neurons were shown to be exclusively GABAergic, suggesting that the contribution of glutamatergic neurons to physiological synchronization processes at early postnatal stages is minimal. However, without fast GABAergic transmission, a different situation may prevail. In the adult CA3, blocking fast GABAergic transmission induces the generation of network bursts that can be triggered by the stimulation of single pyramidal neurons. Here we revisit the network function of CA3 glutamatergic neurons from a developmental viewpoint, without fast GABAergic transmission. We uncover a sub-population of early-generated glutamatergic neurons that impacts network dynamics when stimulated in the juvenile hippocampus. Additionally, this population displays characteristic morpho-physiological features in the juvenile and adult hippocampus. Therefore, the apparently homogeneous glutamatergic cell population likely displays a morpho-functional diversity rooted in temporal embryonic origins. Nature Pub. Group 2012-12-27 /pmc/articles/PMC3535425/ /pubmed/23271650 http://dx.doi.org/10.1038/ncomms2318 Text en Copyright © 2012, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Marissal, Thomas
Bonifazi, Paolo
Picardo, Michel Aimé
Nardou, Romain
Petit, Ludovic Franck
Baude, Agnès
Fishell, Gordon James
Ben-Ari, Yehezkel
Cossart, Rosa
Pioneer glutamatergic cells develop into a morpho-functionally distinct population in the juvenile CA3 hippocampus
title Pioneer glutamatergic cells develop into a morpho-functionally distinct population in the juvenile CA3 hippocampus
title_full Pioneer glutamatergic cells develop into a morpho-functionally distinct population in the juvenile CA3 hippocampus
title_fullStr Pioneer glutamatergic cells develop into a morpho-functionally distinct population in the juvenile CA3 hippocampus
title_full_unstemmed Pioneer glutamatergic cells develop into a morpho-functionally distinct population in the juvenile CA3 hippocampus
title_short Pioneer glutamatergic cells develop into a morpho-functionally distinct population in the juvenile CA3 hippocampus
title_sort pioneer glutamatergic cells develop into a morpho-functionally distinct population in the juvenile ca3 hippocampus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3535425/
https://www.ncbi.nlm.nih.gov/pubmed/23271650
http://dx.doi.org/10.1038/ncomms2318
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