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Causal evidence for retina dependent and independent visual motion computations in mouse cortex
How neuronal computations in the sensory periphery contribute to computations in the cortex is not well understood. We examined this question in the context of visual-motion processing in the retina and primary visual cortex (V1) of mice. We disrupted retinal direction selectivity – either exclusive...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490790/ https://www.ncbi.nlm.nih.gov/pubmed/28530661 http://dx.doi.org/10.1038/nn.4566 |
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author | Hillier, Daniel Fiscella, Michele Drinnenberg, Antonia Trenholm, Stuart Rompani, Santiago B. Raics, Zoltan Katona, Gergely Juettner, Josephine Hierlemann, Andreas Rozsa, Balazs Roska, Botond |
author_facet | Hillier, Daniel Fiscella, Michele Drinnenberg, Antonia Trenholm, Stuart Rompani, Santiago B. Raics, Zoltan Katona, Gergely Juettner, Josephine Hierlemann, Andreas Rozsa, Balazs Roska, Botond |
author_sort | Hillier, Daniel |
collection | PubMed |
description | How neuronal computations in the sensory periphery contribute to computations in the cortex is not well understood. We examined this question in the context of visual-motion processing in the retina and primary visual cortex (V1) of mice. We disrupted retinal direction selectivity – either exclusively along the horizontal axis using FRMD7 mutants or along all directions by ablating starburst amacrine cells – and monitored neuronal activity in layer 2/3 of V1 during stimulation with visual motion. In control mice, we found an overrepresentation of cortical cells preferring posterior visual motion, the dominant motion direction an animal experiences when it moves forward. In mice with disrupted retinal direction selectivity, the overrepresentation of posterior-motion-preferring cortical cells disappeared, and their response at higher stimulus speeds was reduced. This work reveals the existence of two functionally distinct, sensory-periphery-dependent and -independent computations of visual motion in the cortex. |
format | Online Article Text |
id | pubmed-5490790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-54907902017-11-22 Causal evidence for retina dependent and independent visual motion computations in mouse cortex Hillier, Daniel Fiscella, Michele Drinnenberg, Antonia Trenholm, Stuart Rompani, Santiago B. Raics, Zoltan Katona, Gergely Juettner, Josephine Hierlemann, Andreas Rozsa, Balazs Roska, Botond Nat Neurosci Article How neuronal computations in the sensory periphery contribute to computations in the cortex is not well understood. We examined this question in the context of visual-motion processing in the retina and primary visual cortex (V1) of mice. We disrupted retinal direction selectivity – either exclusively along the horizontal axis using FRMD7 mutants or along all directions by ablating starburst amacrine cells – and monitored neuronal activity in layer 2/3 of V1 during stimulation with visual motion. In control mice, we found an overrepresentation of cortical cells preferring posterior visual motion, the dominant motion direction an animal experiences when it moves forward. In mice with disrupted retinal direction selectivity, the overrepresentation of posterior-motion-preferring cortical cells disappeared, and their response at higher stimulus speeds was reduced. This work reveals the existence of two functionally distinct, sensory-periphery-dependent and -independent computations of visual motion in the cortex. 2017-05-22 2017-07 /pmc/articles/PMC5490790/ /pubmed/28530661 http://dx.doi.org/10.1038/nn.4566 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 Hillier, Daniel Fiscella, Michele Drinnenberg, Antonia Trenholm, Stuart Rompani, Santiago B. Raics, Zoltan Katona, Gergely Juettner, Josephine Hierlemann, Andreas Rozsa, Balazs Roska, Botond Causal evidence for retina dependent and independent visual motion computations in mouse cortex |
title | Causal evidence for retina dependent and independent visual motion computations in mouse cortex |
title_full | Causal evidence for retina dependent and independent visual motion computations in mouse cortex |
title_fullStr | Causal evidence for retina dependent and independent visual motion computations in mouse cortex |
title_full_unstemmed | Causal evidence for retina dependent and independent visual motion computations in mouse cortex |
title_short | Causal evidence for retina dependent and independent visual motion computations in mouse cortex |
title_sort | causal evidence for retina dependent and independent visual motion computations in mouse cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490790/ https://www.ncbi.nlm.nih.gov/pubmed/28530661 http://dx.doi.org/10.1038/nn.4566 |
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