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Entorhinal Neurons Exhibit Cue Locking in Rodent VR

The regular firing pattern exhibited by medial entorhinal (mEC) grid cells of locomoting rodents is hypothesized to provide spatial metric information relevant for navigation. The development of virtual reality (VR) for head-fixed mice confers a number of experimental advantages and has become incre...

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Autores principales: Casali, Giulio, Shipley, Sarah, Dowell, Charlie, Hayman, Robin, Barry, Caswell
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344450/
https://www.ncbi.nlm.nih.gov/pubmed/30705621
http://dx.doi.org/10.3389/fncel.2018.00512
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author Casali, Giulio
Shipley, Sarah
Dowell, Charlie
Hayman, Robin
Barry, Caswell
author_facet Casali, Giulio
Shipley, Sarah
Dowell, Charlie
Hayman, Robin
Barry, Caswell
author_sort Casali, Giulio
collection PubMed
description The regular firing pattern exhibited by medial entorhinal (mEC) grid cells of locomoting rodents is hypothesized to provide spatial metric information relevant for navigation. The development of virtual reality (VR) for head-fixed mice confers a number of experimental advantages and has become increasingly popular as a method for investigating spatially-selective cells. Recent experiments using 1D VR linear tracks have shown that some mEC cells have multiple fields in virtual space, analogous to grid cells on real linear tracks. We recorded from the mEC as mice traversed virtual tracks featuring regularly spaced repetitive cues and identified a population of cells with multiple firing fields, resembling the regular firing of grid cells. However, further analyses indicated that many of these were not, in fact, grid cells because: (1) when recorded in the open field they did not display discrete firing fields with six-fold symmetry; and (2) in different VR environments their firing fields were found to match the spatial frequency of repetitive environmental cues. In contrast, cells identified as grid cells based on their open field firing patterns did not exhibit cue locking. In light of these results we highlight the importance of controlling the periodicity of the visual cues in VR and the necessity of identifying grid cells from real open field environments in order to correctly characterize spatially modulated neurons in VR experiments.
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spelling pubmed-63444502019-01-31 Entorhinal Neurons Exhibit Cue Locking in Rodent VR Casali, Giulio Shipley, Sarah Dowell, Charlie Hayman, Robin Barry, Caswell Front Cell Neurosci Neuroscience The regular firing pattern exhibited by medial entorhinal (mEC) grid cells of locomoting rodents is hypothesized to provide spatial metric information relevant for navigation. The development of virtual reality (VR) for head-fixed mice confers a number of experimental advantages and has become increasingly popular as a method for investigating spatially-selective cells. Recent experiments using 1D VR linear tracks have shown that some mEC cells have multiple fields in virtual space, analogous to grid cells on real linear tracks. We recorded from the mEC as mice traversed virtual tracks featuring regularly spaced repetitive cues and identified a population of cells with multiple firing fields, resembling the regular firing of grid cells. However, further analyses indicated that many of these were not, in fact, grid cells because: (1) when recorded in the open field they did not display discrete firing fields with six-fold symmetry; and (2) in different VR environments their firing fields were found to match the spatial frequency of repetitive environmental cues. In contrast, cells identified as grid cells based on their open field firing patterns did not exhibit cue locking. In light of these results we highlight the importance of controlling the periodicity of the visual cues in VR and the necessity of identifying grid cells from real open field environments in order to correctly characterize spatially modulated neurons in VR experiments. Frontiers Media S.A. 2019-01-17 /pmc/articles/PMC6344450/ /pubmed/30705621 http://dx.doi.org/10.3389/fncel.2018.00512 Text en Copyright © 2019 Casali, Shipley, Dowell, Hayman and Barry. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Casali, Giulio
Shipley, Sarah
Dowell, Charlie
Hayman, Robin
Barry, Caswell
Entorhinal Neurons Exhibit Cue Locking in Rodent VR
title Entorhinal Neurons Exhibit Cue Locking in Rodent VR
title_full Entorhinal Neurons Exhibit Cue Locking in Rodent VR
title_fullStr Entorhinal Neurons Exhibit Cue Locking in Rodent VR
title_full_unstemmed Entorhinal Neurons Exhibit Cue Locking in Rodent VR
title_short Entorhinal Neurons Exhibit Cue Locking in Rodent VR
title_sort entorhinal neurons exhibit cue locking in rodent vr
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344450/
https://www.ncbi.nlm.nih.gov/pubmed/30705621
http://dx.doi.org/10.3389/fncel.2018.00512
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