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Cell Type-Specific Separation of Subicular Principal Neurons during Network Activities
The hippocampal output structure, the subiculum, expresses two major memory relevant network rhythms, sharp wave ripple and gamma frequency oscillations. To this date, it remains unclear how the two distinct types of subicular principal cells, intrinsically bursting and regular spiking neurons, part...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396839/ https://www.ncbi.nlm.nih.gov/pubmed/25874555 http://dx.doi.org/10.1371/journal.pone.0123636 |
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author | Eller, Joanna Zarnadze, Shota Bäuerle, Peter Dugladze, Tamar Gloveli, Tengis |
author_facet | Eller, Joanna Zarnadze, Shota Bäuerle, Peter Dugladze, Tamar Gloveli, Tengis |
author_sort | Eller, Joanna |
collection | PubMed |
description | The hippocampal output structure, the subiculum, expresses two major memory relevant network rhythms, sharp wave ripple and gamma frequency oscillations. To this date, it remains unclear how the two distinct types of subicular principal cells, intrinsically bursting and regular spiking neurons, participate in these two network rhythms. Using concomitant local field potential and intracellular recordings in an in vitro mouse model that allows the investigation of both network rhythms, we found a cell type-specific segregation of principal neurons into participating intrinsically bursting and non-participating regular spiking cells. However, if regular spiking cells were kept at a more depolarized level, they did participate in a specific manner, suggesting a potential bimodal working model dependent on the level of excitation. Furthermore, intrinsically bursting and regular spiking cells exhibited divergent intrinsic membrane and synaptic properties in the active network. Thus, our results suggest a cell-type-specific segregation of principal cells into two separate groups during network activities, supporting the idea of two parallel streams of information processing within the subiculum. |
format | Online Article Text |
id | pubmed-4396839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43968392015-04-21 Cell Type-Specific Separation of Subicular Principal Neurons during Network Activities Eller, Joanna Zarnadze, Shota Bäuerle, Peter Dugladze, Tamar Gloveli, Tengis PLoS One Research Article The hippocampal output structure, the subiculum, expresses two major memory relevant network rhythms, sharp wave ripple and gamma frequency oscillations. To this date, it remains unclear how the two distinct types of subicular principal cells, intrinsically bursting and regular spiking neurons, participate in these two network rhythms. Using concomitant local field potential and intracellular recordings in an in vitro mouse model that allows the investigation of both network rhythms, we found a cell type-specific segregation of principal neurons into participating intrinsically bursting and non-participating regular spiking cells. However, if regular spiking cells were kept at a more depolarized level, they did participate in a specific manner, suggesting a potential bimodal working model dependent on the level of excitation. Furthermore, intrinsically bursting and regular spiking cells exhibited divergent intrinsic membrane and synaptic properties in the active network. Thus, our results suggest a cell-type-specific segregation of principal cells into two separate groups during network activities, supporting the idea of two parallel streams of information processing within the subiculum. Public Library of Science 2015-04-14 /pmc/articles/PMC4396839/ /pubmed/25874555 http://dx.doi.org/10.1371/journal.pone.0123636 Text en © 2015 Eller et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Eller, Joanna Zarnadze, Shota Bäuerle, Peter Dugladze, Tamar Gloveli, Tengis Cell Type-Specific Separation of Subicular Principal Neurons during Network Activities |
title | Cell Type-Specific Separation of Subicular Principal Neurons during Network Activities |
title_full | Cell Type-Specific Separation of Subicular Principal Neurons during Network Activities |
title_fullStr | Cell Type-Specific Separation of Subicular Principal Neurons during Network Activities |
title_full_unstemmed | Cell Type-Specific Separation of Subicular Principal Neurons during Network Activities |
title_short | Cell Type-Specific Separation of Subicular Principal Neurons during Network Activities |
title_sort | cell type-specific separation of subicular principal neurons during network activities |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396839/ https://www.ncbi.nlm.nih.gov/pubmed/25874555 http://dx.doi.org/10.1371/journal.pone.0123636 |
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