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Pattern Motion Processing by MT Neurons

Based on stimulation with plaid patterns, neurons in the Middle Temporal (MT) area of primate visual cortex are divided into two types: pattern and component cells. The prevailing theory suggests that pattern selectivity results from the summation of the outputs of component cells as part of a hiera...

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Autores principales: Zarei Eskikand, Parvin, Kameneva, Tatiana, Burkitt, Anthony N., Grayden, David B., Ibbotson, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598444/
https://www.ncbi.nlm.nih.gov/pubmed/31293393
http://dx.doi.org/10.3389/fncir.2019.00043
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author Zarei Eskikand, Parvin
Kameneva, Tatiana
Burkitt, Anthony N.
Grayden, David B.
Ibbotson, Michael R.
author_facet Zarei Eskikand, Parvin
Kameneva, Tatiana
Burkitt, Anthony N.
Grayden, David B.
Ibbotson, Michael R.
author_sort Zarei Eskikand, Parvin
collection PubMed
description Based on stimulation with plaid patterns, neurons in the Middle Temporal (MT) area of primate visual cortex are divided into two types: pattern and component cells. The prevailing theory suggests that pattern selectivity results from the summation of the outputs of component cells as part of a hierarchical visual pathway. We present a computational model of the visual pathway from primary visual cortex (V1) to MT that suggests an alternate model where the progression from component to pattern selectivity is not required. Using standard orientation-selective V1 cells, end-stopped V1 cells, and V1 cells with extra-classical receptive fields (RFs) as inputs to MT, the model shows that the degree of pattern or component selectivity in MT could arise from the relative strengths of the three V1 input types. Dominance of end-stopped V1 neurons in the model leads to pattern selectivity in MT, while dominance of V1 cells with extra-classical RFs result in component selectivity. This model may assist in designing experiments to further understand motion processing mechanisms in primate MT.
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spelling pubmed-65984442019-07-10 Pattern Motion Processing by MT Neurons Zarei Eskikand, Parvin Kameneva, Tatiana Burkitt, Anthony N. Grayden, David B. Ibbotson, Michael R. Front Neural Circuits Neuroscience Based on stimulation with plaid patterns, neurons in the Middle Temporal (MT) area of primate visual cortex are divided into two types: pattern and component cells. The prevailing theory suggests that pattern selectivity results from the summation of the outputs of component cells as part of a hierarchical visual pathway. We present a computational model of the visual pathway from primary visual cortex (V1) to MT that suggests an alternate model where the progression from component to pattern selectivity is not required. Using standard orientation-selective V1 cells, end-stopped V1 cells, and V1 cells with extra-classical receptive fields (RFs) as inputs to MT, the model shows that the degree of pattern or component selectivity in MT could arise from the relative strengths of the three V1 input types. Dominance of end-stopped V1 neurons in the model leads to pattern selectivity in MT, while dominance of V1 cells with extra-classical RFs result in component selectivity. This model may assist in designing experiments to further understand motion processing mechanisms in primate MT. Frontiers Media S.A. 2019-06-21 /pmc/articles/PMC6598444/ /pubmed/31293393 http://dx.doi.org/10.3389/fncir.2019.00043 Text en Copyright © 2019 Zarei Eskikand, Kameneva, Burkitt, Grayden and Ibbotson. http://creativecommons.org/licenses/by/4.0/ 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) and the copyright owner(s) 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
Zarei Eskikand, Parvin
Kameneva, Tatiana
Burkitt, Anthony N.
Grayden, David B.
Ibbotson, Michael R.
Pattern Motion Processing by MT Neurons
title Pattern Motion Processing by MT Neurons
title_full Pattern Motion Processing by MT Neurons
title_fullStr Pattern Motion Processing by MT Neurons
title_full_unstemmed Pattern Motion Processing by MT Neurons
title_short Pattern Motion Processing by MT Neurons
title_sort pattern motion processing by mt neurons
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598444/
https://www.ncbi.nlm.nih.gov/pubmed/31293393
http://dx.doi.org/10.3389/fncir.2019.00043
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