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Coherent encoding of subjective spatial position in visual cortex and hippocampus
A major role of vision is to guide navigation, and navigation is strongly driven by vision1–4. Indeed, the brain’s visual and navigational systems are known to interact5,6, and signals related to position in the environment have been suggested to appear as early as in visual cortex6,7. To establish...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6309439/ https://www.ncbi.nlm.nih.gov/pubmed/30202092 http://dx.doi.org/10.1038/s41586-018-0516-1 |
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author | Saleem, Aman B. Diamanti, E. Mika Fournier, Julien Harris, Kenneth D. Carandini, Matteo |
author_facet | Saleem, Aman B. Diamanti, E. Mika Fournier, Julien Harris, Kenneth D. Carandini, Matteo |
author_sort | Saleem, Aman B. |
collection | PubMed |
description | A major role of vision is to guide navigation, and navigation is strongly driven by vision1–4. Indeed, the brain’s visual and navigational systems are known to interact5,6, and signals related to position in the environment have been suggested to appear as early as in visual cortex6,7. To establish the nature of these signals we recorded in primary visual cortex (V1) and in hippocampal area CA1 while mice traversed a corridor in virtual reality. The corridor contained identical visual landmarks in two positions, so that a purely visual neuron would respond similarly in those positions. Most V1 neurons, however, responded solely or more strongly to the landmarks in one position. This modulation of visual responses by spatial location was not explained by factors such as running speed. To assess whether the modulation is related to navigational signals and to the animal’s subjective estimate of position, we trained the mice to lick for a water reward upon reaching a reward zone in the corridor. Neuronal populations in both CA1 and V1 encoded the animal’s position along the corridor, and the errors in their representations were correlated. Moreover, both representations reflected the animal’s subjective estimate of position, inferred from the animal’s licks, better than its actual position. Indeed, when animals licked in a given location – whether correct or incorrect – neural populations in both V1 and CA1 placed the animal in the reward zone. We conclude that visual responses in V1 are controlled by navigational signals, which are coherent with those encoded in hippocampus and reflect the animal’s subjective position. The presence of such navigational signals as early as in a primary sensory area suggests that they permeate sensory processing in the cortex. |
format | Online Article Text |
id | pubmed-6309439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-63094392019-03-10 Coherent encoding of subjective spatial position in visual cortex and hippocampus Saleem, Aman B. Diamanti, E. Mika Fournier, Julien Harris, Kenneth D. Carandini, Matteo Nature Article A major role of vision is to guide navigation, and navigation is strongly driven by vision1–4. Indeed, the brain’s visual and navigational systems are known to interact5,6, and signals related to position in the environment have been suggested to appear as early as in visual cortex6,7. To establish the nature of these signals we recorded in primary visual cortex (V1) and in hippocampal area CA1 while mice traversed a corridor in virtual reality. The corridor contained identical visual landmarks in two positions, so that a purely visual neuron would respond similarly in those positions. Most V1 neurons, however, responded solely or more strongly to the landmarks in one position. This modulation of visual responses by spatial location was not explained by factors such as running speed. To assess whether the modulation is related to navigational signals and to the animal’s subjective estimate of position, we trained the mice to lick for a water reward upon reaching a reward zone in the corridor. Neuronal populations in both CA1 and V1 encoded the animal’s position along the corridor, and the errors in their representations were correlated. Moreover, both representations reflected the animal’s subjective estimate of position, inferred from the animal’s licks, better than its actual position. Indeed, when animals licked in a given location – whether correct or incorrect – neural populations in both V1 and CA1 placed the animal in the reward zone. We conclude that visual responses in V1 are controlled by navigational signals, which are coherent with those encoded in hippocampus and reflect the animal’s subjective position. The presence of such navigational signals as early as in a primary sensory area suggests that they permeate sensory processing in the cortex. 2018-09-10 2018-10 /pmc/articles/PMC6309439/ /pubmed/30202092 http://dx.doi.org/10.1038/s41586-018-0516-1 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 Saleem, Aman B. Diamanti, E. Mika Fournier, Julien Harris, Kenneth D. Carandini, Matteo Coherent encoding of subjective spatial position in visual cortex and hippocampus |
title | Coherent encoding of subjective spatial position in visual cortex and hippocampus |
title_full | Coherent encoding of subjective spatial position in visual cortex and hippocampus |
title_fullStr | Coherent encoding of subjective spatial position in visual cortex and hippocampus |
title_full_unstemmed | Coherent encoding of subjective spatial position in visual cortex and hippocampus |
title_short | Coherent encoding of subjective spatial position in visual cortex and hippocampus |
title_sort | coherent encoding of subjective spatial position in visual cortex and hippocampus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6309439/ https://www.ncbi.nlm.nih.gov/pubmed/30202092 http://dx.doi.org/10.1038/s41586-018-0516-1 |
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