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Egocentric boundary vector tuning of the retrosplenial cortex
The retrosplenial cortex is reciprocally connected with multiple structures implicated in spatial cognition, and damage to the region itself produces numerous spatial impairments. Here, we sought to characterize spatial correlates of neurons within the region during free exploration in two-dimension...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035004/ https://www.ncbi.nlm.nih.gov/pubmed/32128423 http://dx.doi.org/10.1126/sciadv.aaz2322 |
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author | Alexander, Andrew S. Carstensen, Lucas C. Hinman, James R. Raudies, Florian Chapman, G. William Hasselmo, Michael E. |
author_facet | Alexander, Andrew S. Carstensen, Lucas C. Hinman, James R. Raudies, Florian Chapman, G. William Hasselmo, Michael E. |
author_sort | Alexander, Andrew S. |
collection | PubMed |
description | The retrosplenial cortex is reciprocally connected with multiple structures implicated in spatial cognition, and damage to the region itself produces numerous spatial impairments. Here, we sought to characterize spatial correlates of neurons within the region during free exploration in two-dimensional environments. We report that a large percentage of retrosplenial cortex neurons have spatial receptive fields that are active when environmental boundaries are positioned at a specific orientation and distance relative to the animal itself. We demonstrate that this vector-based location signal is encoded in egocentric coordinates, is localized to the dysgranular retrosplenial subregion, is independent of self-motion, and is context invariant. Further, we identify a subpopulation of neurons with this response property that are synchronized with the hippocampal theta oscillation. Accordingly, the current work identifies a robust egocentric spatial code in retrosplenial cortex that can facilitate spatial coordinate system transformations and support the anchoring, generation, and utilization of allocentric representations. |
format | Online Article Text |
id | pubmed-7035004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-70350042020-03-03 Egocentric boundary vector tuning of the retrosplenial cortex Alexander, Andrew S. Carstensen, Lucas C. Hinman, James R. Raudies, Florian Chapman, G. William Hasselmo, Michael E. Sci Adv Research Articles The retrosplenial cortex is reciprocally connected with multiple structures implicated in spatial cognition, and damage to the region itself produces numerous spatial impairments. Here, we sought to characterize spatial correlates of neurons within the region during free exploration in two-dimensional environments. We report that a large percentage of retrosplenial cortex neurons have spatial receptive fields that are active when environmental boundaries are positioned at a specific orientation and distance relative to the animal itself. We demonstrate that this vector-based location signal is encoded in egocentric coordinates, is localized to the dysgranular retrosplenial subregion, is independent of self-motion, and is context invariant. Further, we identify a subpopulation of neurons with this response property that are synchronized with the hippocampal theta oscillation. Accordingly, the current work identifies a robust egocentric spatial code in retrosplenial cortex that can facilitate spatial coordinate system transformations and support the anchoring, generation, and utilization of allocentric representations. American Association for the Advancement of Science 2020-02-21 /pmc/articles/PMC7035004/ /pubmed/32128423 http://dx.doi.org/10.1126/sciadv.aaz2322 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Alexander, Andrew S. Carstensen, Lucas C. Hinman, James R. Raudies, Florian Chapman, G. William Hasselmo, Michael E. Egocentric boundary vector tuning of the retrosplenial cortex |
title | Egocentric boundary vector tuning of the retrosplenial cortex |
title_full | Egocentric boundary vector tuning of the retrosplenial cortex |
title_fullStr | Egocentric boundary vector tuning of the retrosplenial cortex |
title_full_unstemmed | Egocentric boundary vector tuning of the retrosplenial cortex |
title_short | Egocentric boundary vector tuning of the retrosplenial cortex |
title_sort | egocentric boundary vector tuning of the retrosplenial cortex |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035004/ https://www.ncbi.nlm.nih.gov/pubmed/32128423 http://dx.doi.org/10.1126/sciadv.aaz2322 |
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