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Entorhinal velocity signals reflect environmental geometry
The entorhinal cortex contains neurons that represent self-location, including grid cells that fire in periodic locations and velocity signals that encode running speed and head direction. While the size and shape of the environment influences grid patterns, whether entorhinal velocity signals are e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007349/ https://www.ncbi.nlm.nih.gov/pubmed/31932764 http://dx.doi.org/10.1038/s41593-019-0562-5 |
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author | Munn, Robert G K Mallory, Caitlin S Hardcastle, Kiah Chetkovich, Dane M Giocomo, Lisa M |
author_facet | Munn, Robert G K Mallory, Caitlin S Hardcastle, Kiah Chetkovich, Dane M Giocomo, Lisa M |
author_sort | Munn, Robert G K |
collection | PubMed |
description | The entorhinal cortex contains neurons that represent self-location, including grid cells that fire in periodic locations and velocity signals that encode running speed and head direction. While the size and shape of the environment influences grid patterns, whether entorhinal velocity signals are equally influenced or provide a universal metric for self-motion across environments remains unknown. Here, we report that speed cells rescale after changes to the size and shape of the environment. Moreover, head direction cells re-organize in an experience-dependent manner to align with the axis of environmental change. A knockout mouse model allows a dissociation of the coordination between cell types, with grid and speed, but not head direction, cells responding in concert to environmental change. These results point to malleability in the coding features of multiple entorhinal cell types and have implications for which cell types contribute to the velocity signal used by computational models of grid cells. |
format | Online Article Text |
id | pubmed-7007349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-70073492020-07-13 Entorhinal velocity signals reflect environmental geometry Munn, Robert G K Mallory, Caitlin S Hardcastle, Kiah Chetkovich, Dane M Giocomo, Lisa M Nat Neurosci Article The entorhinal cortex contains neurons that represent self-location, including grid cells that fire in periodic locations and velocity signals that encode running speed and head direction. While the size and shape of the environment influences grid patterns, whether entorhinal velocity signals are equally influenced or provide a universal metric for self-motion across environments remains unknown. Here, we report that speed cells rescale after changes to the size and shape of the environment. Moreover, head direction cells re-organize in an experience-dependent manner to align with the axis of environmental change. A knockout mouse model allows a dissociation of the coordination between cell types, with grid and speed, but not head direction, cells responding in concert to environmental change. These results point to malleability in the coding features of multiple entorhinal cell types and have implications for which cell types contribute to the velocity signal used by computational models of grid cells. 2020-01-13 2020-02 /pmc/articles/PMC7007349/ /pubmed/31932764 http://dx.doi.org/10.1038/s41593-019-0562-5 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Munn, Robert G K Mallory, Caitlin S Hardcastle, Kiah Chetkovich, Dane M Giocomo, Lisa M Entorhinal velocity signals reflect environmental geometry |
title | Entorhinal velocity signals reflect environmental geometry |
title_full | Entorhinal velocity signals reflect environmental geometry |
title_fullStr | Entorhinal velocity signals reflect environmental geometry |
title_full_unstemmed | Entorhinal velocity signals reflect environmental geometry |
title_short | Entorhinal velocity signals reflect environmental geometry |
title_sort | entorhinal velocity signals reflect environmental geometry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007349/ https://www.ncbi.nlm.nih.gov/pubmed/31932764 http://dx.doi.org/10.1038/s41593-019-0562-5 |
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