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Recovering stimulus locations using populations of eye-position modulated neurons in dorsal and ventral visual streams of non-human primates
We recorded visual responses while monkeys fixated the same target at different gaze angles, both dorsally (lateral intraparietal cortex, LIP) and ventrally (anterior inferotemporal cortex, AIT). While eye-position modulations occurred in both areas, they were both more frequent and stronger in LIP...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975102/ https://www.ncbi.nlm.nih.gov/pubmed/24734008 http://dx.doi.org/10.3389/fnint.2014.00028 |
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author | Sereno, Anne B. Sereno, Margaret E. Lehky, Sidney R. |
author_facet | Sereno, Anne B. Sereno, Margaret E. Lehky, Sidney R. |
author_sort | Sereno, Anne B. |
collection | PubMed |
description | We recorded visual responses while monkeys fixated the same target at different gaze angles, both dorsally (lateral intraparietal cortex, LIP) and ventrally (anterior inferotemporal cortex, AIT). While eye-position modulations occurred in both areas, they were both more frequent and stronger in LIP neurons. We used an intrinsic population decoding technique, multidimensional scaling (MDS), to recover eye positions, equivalent to recovering fixated target locations. We report that eye-position based visual space in LIP was more accurate (i.e., metric). Nevertheless, the AIT spatial representation remained largely topologically correct, perhaps indicative of a categorical spatial representation (i.e., a qualitative description such as “left of” or “above” as opposed to a quantitative, metrically precise description). Additionally, we developed a simple neural model of eye position signals and illustrate that differences in single cell characteristics can influence the ability to recover target position in a population of cells. We demonstrate for the first time that the ventral stream contains sufficient information for constructing an eye-position based spatial representation. Furthermore we demonstrate, in dorsal and ventral streams as well as modeling, that target locations can be extracted directly from eye position signals in cortical visual responses without computing coordinate transforms of visual space. |
format | Online Article Text |
id | pubmed-3975102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39751022014-04-14 Recovering stimulus locations using populations of eye-position modulated neurons in dorsal and ventral visual streams of non-human primates Sereno, Anne B. Sereno, Margaret E. Lehky, Sidney R. Front Integr Neurosci Neuroscience We recorded visual responses while monkeys fixated the same target at different gaze angles, both dorsally (lateral intraparietal cortex, LIP) and ventrally (anterior inferotemporal cortex, AIT). While eye-position modulations occurred in both areas, they were both more frequent and stronger in LIP neurons. We used an intrinsic population decoding technique, multidimensional scaling (MDS), to recover eye positions, equivalent to recovering fixated target locations. We report that eye-position based visual space in LIP was more accurate (i.e., metric). Nevertheless, the AIT spatial representation remained largely topologically correct, perhaps indicative of a categorical spatial representation (i.e., a qualitative description such as “left of” or “above” as opposed to a quantitative, metrically precise description). Additionally, we developed a simple neural model of eye position signals and illustrate that differences in single cell characteristics can influence the ability to recover target position in a population of cells. We demonstrate for the first time that the ventral stream contains sufficient information for constructing an eye-position based spatial representation. Furthermore we demonstrate, in dorsal and ventral streams as well as modeling, that target locations can be extracted directly from eye position signals in cortical visual responses without computing coordinate transforms of visual space. Frontiers Media S.A. 2014-03-28 /pmc/articles/PMC3975102/ /pubmed/24734008 http://dx.doi.org/10.3389/fnint.2014.00028 Text en Copyright © 2014 Sereno, Sereno and Lehky. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Sereno, Anne B. Sereno, Margaret E. Lehky, Sidney R. Recovering stimulus locations using populations of eye-position modulated neurons in dorsal and ventral visual streams of non-human primates |
title | Recovering stimulus locations using populations of eye-position modulated neurons in dorsal and ventral visual streams of non-human primates |
title_full | Recovering stimulus locations using populations of eye-position modulated neurons in dorsal and ventral visual streams of non-human primates |
title_fullStr | Recovering stimulus locations using populations of eye-position modulated neurons in dorsal and ventral visual streams of non-human primates |
title_full_unstemmed | Recovering stimulus locations using populations of eye-position modulated neurons in dorsal and ventral visual streams of non-human primates |
title_short | Recovering stimulus locations using populations of eye-position modulated neurons in dorsal and ventral visual streams of non-human primates |
title_sort | recovering stimulus locations using populations of eye-position modulated neurons in dorsal and ventral visual streams of non-human primates |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975102/ https://www.ncbi.nlm.nih.gov/pubmed/24734008 http://dx.doi.org/10.3389/fnint.2014.00028 |
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