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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...

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Autores principales: Alexander, Andrew S., Carstensen, Lucas C., Hinman, James R., Raudies, Florian, Chapman, G. William, Hasselmo, Michael E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
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.
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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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