A neural-level model of spatial memory and imagery
We present a model of how neural representations of egocentric spatial experiences in parietal cortex interface with viewpoint-independent representations in medial temporal areas, via retrosplenial cortex, to enable many key aspects of spatial cognition. This account shows how previously reported n...
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2018-09-01
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doaj-3d1db15fbc24434e89e8f29c5119470b2021-05-05T16:08:04ZengeLife Sciences Publications LtdeLife2050-084X2018-09-01710.7554/eLife.33752A neural-level model of spatial memory and imageryAndrej Bicanski0https://orcid.org/0000-0003-3356-1034Neil Burgess1https://orcid.org/0000-0003-0646-6584Institute of Cognitive Neuroscience, University College London, London, United KingdomInstitute of Cognitive Neuroscience, University College London, London, United KingdomWe present a model of how neural representations of egocentric spatial experiences in parietal cortex interface with viewpoint-independent representations in medial temporal areas, via retrosplenial cortex, to enable many key aspects of spatial cognition. This account shows how previously reported neural responses (place, head-direction and grid cells, allocentric boundary- and object-vector cells, gain-field neurons) can map onto higher cognitive function in a modular way, and predicts new cell types (egocentric and head-direction-modulated boundary- and object-vector cells). The model predicts how these neural populations should interact across multiple brain regions to support spatial memory, scene construction, novelty-detection, ‘trace cells’, and mental navigation. Simulated behavior and firing rate maps are compared to experimental data, for example showing how object-vector cells allow items to be remembered within a contextual representation based on environmental boundaries, and how grid cells could update the viewpoint in imagery during planning and short-cutting by driving sequential place cell activity.https://elifesciences.org/articles/33752computational modelepisodic memoryspatially selective cellsspatial cognitionscene constructiontrace cells |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Andrej Bicanski Neil Burgess |
spellingShingle |
Andrej Bicanski Neil Burgess A neural-level model of spatial memory and imagery eLife computational model episodic memory spatially selective cells spatial cognition scene construction trace cells |
author_facet |
Andrej Bicanski Neil Burgess |
author_sort |
Andrej Bicanski |
title |
A neural-level model of spatial memory and imagery |
title_short |
A neural-level model of spatial memory and imagery |
title_full |
A neural-level model of spatial memory and imagery |
title_fullStr |
A neural-level model of spatial memory and imagery |
title_full_unstemmed |
A neural-level model of spatial memory and imagery |
title_sort |
neural-level model of spatial memory and imagery |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2018-09-01 |
description |
We present a model of how neural representations of egocentric spatial experiences in parietal cortex interface with viewpoint-independent representations in medial temporal areas, via retrosplenial cortex, to enable many key aspects of spatial cognition. This account shows how previously reported neural responses (place, head-direction and grid cells, allocentric boundary- and object-vector cells, gain-field neurons) can map onto higher cognitive function in a modular way, and predicts new cell types (egocentric and head-direction-modulated boundary- and object-vector cells). The model predicts how these neural populations should interact across multiple brain regions to support spatial memory, scene construction, novelty-detection, ‘trace cells’, and mental navigation. Simulated behavior and firing rate maps are compared to experimental data, for example showing how object-vector cells allow items to be remembered within a contextual representation based on environmental boundaries, and how grid cells could update the viewpoint in imagery during planning and short-cutting by driving sequential place cell activity. |
topic |
computational model episodic memory spatially selective cells spatial cognition scene construction trace cells |
url |
https://elifesciences.org/articles/33752 |
work_keys_str_mv |
AT andrejbicanski aneurallevelmodelofspatialmemoryandimagery AT neilburgess aneurallevelmodelofspatialmemoryandimagery AT andrejbicanski neurallevelmodelofspatialmemoryandimagery AT neilburgess neurallevelmodelofspatialmemoryandimagery |
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