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Functional connectivity of the entorhinal–hippocampal space circuit

The mammalian space circuit is known to contain several functionally specialized cell types, such as place cells in the hippocampus and grid cells, head-direction cells and border cells in the medial entorhinal cortex (MEC). The interaction between the entorhinal and hippocampal spatial representati...

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Autores principales: Zhang, Sheng-Jia, Ye, Jing, Couey, Jonathan J., Witter, Menno, Moser, Edvard I., Moser, May-Britt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866440/
https://www.ncbi.nlm.nih.gov/pubmed/24366130
http://dx.doi.org/10.1098/rstb.2012.0516
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author Zhang, Sheng-Jia
Ye, Jing
Couey, Jonathan J.
Witter, Menno
Moser, Edvard I.
Moser, May-Britt
author_facet Zhang, Sheng-Jia
Ye, Jing
Couey, Jonathan J.
Witter, Menno
Moser, Edvard I.
Moser, May-Britt
author_sort Zhang, Sheng-Jia
collection PubMed
description The mammalian space circuit is known to contain several functionally specialized cell types, such as place cells in the hippocampus and grid cells, head-direction cells and border cells in the medial entorhinal cortex (MEC). The interaction between the entorhinal and hippocampal spatial representations is poorly understood, however. We have developed an optogenetic strategy to identify functionally defined cell types in the MEC that project directly to the hippocampus. By expressing channelrhodopsin-2 (ChR2) selectively in the hippocampus-projecting subset of entorhinal projection neurons, we were able to use light-evoked discharge as an instrument to determine whether specific entorhinal cell groups—such as grid cells, border cells and head-direction cells—have direct hippocampal projections. Photoinduced firing was observed at fixed minimal latencies in all functional cell categories, with grid cells as the most abundant hippocampus-projecting spatial cell type. We discuss how photoexcitation experiments can be used to distinguish the subset of hippocampus-projecting entorhinal neurons from neurons that are activated indirectly through the network. The functional breadth of entorhinal input implied by this analysis opens up the potential for rich dynamic interactions between place cells in the hippocampus and different functional cell types in the entorhinal cortex (EC).
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spelling pubmed-38664402014-02-05 Functional connectivity of the entorhinal–hippocampal space circuit Zhang, Sheng-Jia Ye, Jing Couey, Jonathan J. Witter, Menno Moser, Edvard I. Moser, May-Britt Philos Trans R Soc Lond B Biol Sci Part II: Spatial cells: grid, head direction, place and boundary cells The mammalian space circuit is known to contain several functionally specialized cell types, such as place cells in the hippocampus and grid cells, head-direction cells and border cells in the medial entorhinal cortex (MEC). The interaction between the entorhinal and hippocampal spatial representations is poorly understood, however. We have developed an optogenetic strategy to identify functionally defined cell types in the MEC that project directly to the hippocampus. By expressing channelrhodopsin-2 (ChR2) selectively in the hippocampus-projecting subset of entorhinal projection neurons, we were able to use light-evoked discharge as an instrument to determine whether specific entorhinal cell groups—such as grid cells, border cells and head-direction cells—have direct hippocampal projections. Photoinduced firing was observed at fixed minimal latencies in all functional cell categories, with grid cells as the most abundant hippocampus-projecting spatial cell type. We discuss how photoexcitation experiments can be used to distinguish the subset of hippocampus-projecting entorhinal neurons from neurons that are activated indirectly through the network. The functional breadth of entorhinal input implied by this analysis opens up the potential for rich dynamic interactions between place cells in the hippocampus and different functional cell types in the entorhinal cortex (EC). The Royal Society 2014-02-05 /pmc/articles/PMC3866440/ /pubmed/24366130 http://dx.doi.org/10.1098/rstb.2012.0516 Text en http://creativecommons.org/licenses/by/3.0/ © 2013 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Part II: Spatial cells: grid, head direction, place and boundary cells
Zhang, Sheng-Jia
Ye, Jing
Couey, Jonathan J.
Witter, Menno
Moser, Edvard I.
Moser, May-Britt
Functional connectivity of the entorhinal–hippocampal space circuit
title Functional connectivity of the entorhinal–hippocampal space circuit
title_full Functional connectivity of the entorhinal–hippocampal space circuit
title_fullStr Functional connectivity of the entorhinal–hippocampal space circuit
title_full_unstemmed Functional connectivity of the entorhinal–hippocampal space circuit
title_short Functional connectivity of the entorhinal–hippocampal space circuit
title_sort functional connectivity of the entorhinal–hippocampal space circuit
topic Part II: Spatial cells: grid, head direction, place and boundary cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866440/
https://www.ncbi.nlm.nih.gov/pubmed/24366130
http://dx.doi.org/10.1098/rstb.2012.0516
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