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Diverse synaptic and dendritic mechanisms of complex spike burst generation in hippocampal CA3 pyramidal cells

Complex spike bursts (CSBs) represent a characteristic firing pattern of hippocampal pyramidal cells (PCs). In CA1PCs, CSBs are driven by regenerative dendritic plateau potentials, produced by correlated entorhinal cortical and CA3 inputs that simultaneously depolarize distal and proximal dendritic...

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Autores principales: Raus Balind, Snezana, Magó, Ádám, Ahmadi, Mahboobeh, Kis, Noémi, Varga-Németh, Zsófia, Lőrincz, Andrea, Makara, Judit K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478939/
https://www.ncbi.nlm.nih.gov/pubmed/31015414
http://dx.doi.org/10.1038/s41467-019-09767-w
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author Raus Balind, Snezana
Magó, Ádám
Ahmadi, Mahboobeh
Kis, Noémi
Varga-Németh, Zsófia
Lőrincz, Andrea
Makara, Judit K.
author_facet Raus Balind, Snezana
Magó, Ádám
Ahmadi, Mahboobeh
Kis, Noémi
Varga-Németh, Zsófia
Lőrincz, Andrea
Makara, Judit K.
author_sort Raus Balind, Snezana
collection PubMed
description Complex spike bursts (CSBs) represent a characteristic firing pattern of hippocampal pyramidal cells (PCs). In CA1PCs, CSBs are driven by regenerative dendritic plateau potentials, produced by correlated entorhinal cortical and CA3 inputs that simultaneously depolarize distal and proximal dendritic domains. However, in CA3PCs neither the generation mechanisms nor the computational role of CSBs are well elucidated. We show that CSBs are induced by dendritic Ca(2+) spikes in CA3PCs. Surprisingly, the ability of CA3PCs to produce CSBs is heterogeneous, with non-uniform synaptic input-output transformation rules triggering CSBs. The heterogeneity is partly related to the topographic position of CA3PCs; we identify two ion channel types, HCN and Kv2 channels, whose proximodistal activity gradients contribute to subregion-specific modulation of CSB propensity. Our results suggest that heterogeneous dendritic integrative properties, along with previously reported synaptic connectivity gradients, define functional subpopulations of CA3PCs that may support CA3 network computations underlying associative memory processes.
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spelling pubmed-64789392019-04-25 Diverse synaptic and dendritic mechanisms of complex spike burst generation in hippocampal CA3 pyramidal cells Raus Balind, Snezana Magó, Ádám Ahmadi, Mahboobeh Kis, Noémi Varga-Németh, Zsófia Lőrincz, Andrea Makara, Judit K. Nat Commun Article Complex spike bursts (CSBs) represent a characteristic firing pattern of hippocampal pyramidal cells (PCs). In CA1PCs, CSBs are driven by regenerative dendritic plateau potentials, produced by correlated entorhinal cortical and CA3 inputs that simultaneously depolarize distal and proximal dendritic domains. However, in CA3PCs neither the generation mechanisms nor the computational role of CSBs are well elucidated. We show that CSBs are induced by dendritic Ca(2+) spikes in CA3PCs. Surprisingly, the ability of CA3PCs to produce CSBs is heterogeneous, with non-uniform synaptic input-output transformation rules triggering CSBs. The heterogeneity is partly related to the topographic position of CA3PCs; we identify two ion channel types, HCN and Kv2 channels, whose proximodistal activity gradients contribute to subregion-specific modulation of CSB propensity. Our results suggest that heterogeneous dendritic integrative properties, along with previously reported synaptic connectivity gradients, define functional subpopulations of CA3PCs that may support CA3 network computations underlying associative memory processes. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6478939/ /pubmed/31015414 http://dx.doi.org/10.1038/s41467-019-09767-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Raus Balind, Snezana
Magó, Ádám
Ahmadi, Mahboobeh
Kis, Noémi
Varga-Németh, Zsófia
Lőrincz, Andrea
Makara, Judit K.
Diverse synaptic and dendritic mechanisms of complex spike burst generation in hippocampal CA3 pyramidal cells
title Diverse synaptic and dendritic mechanisms of complex spike burst generation in hippocampal CA3 pyramidal cells
title_full Diverse synaptic and dendritic mechanisms of complex spike burst generation in hippocampal CA3 pyramidal cells
title_fullStr Diverse synaptic and dendritic mechanisms of complex spike burst generation in hippocampal CA3 pyramidal cells
title_full_unstemmed Diverse synaptic and dendritic mechanisms of complex spike burst generation in hippocampal CA3 pyramidal cells
title_short Diverse synaptic and dendritic mechanisms of complex spike burst generation in hippocampal CA3 pyramidal cells
title_sort diverse synaptic and dendritic mechanisms of complex spike burst generation in hippocampal ca3 pyramidal cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478939/
https://www.ncbi.nlm.nih.gov/pubmed/31015414
http://dx.doi.org/10.1038/s41467-019-09767-w
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