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Neuronal Correlations in MT and MST Impair Population Decoding of Opposite Directions of Random Dot Motion

The study of neuronal responses to random-dot motion patterns has provided some of the most valuable insights into how the activity of neurons is related to perception. In the opposite directions of motion paradigm, the motion signal strength is decreased by manipulating the coherence of random dot...

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Autores principales: Chaplin, Tristan A., Hagan, Maureen A., Allitt, Benjamin J., Lui, Leo L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327941/
https://www.ncbi.nlm.nih.gov/pubmed/30637327
http://dx.doi.org/10.1523/ENEURO.0336-18.2018
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author Chaplin, Tristan A.
Hagan, Maureen A.
Allitt, Benjamin J.
Lui, Leo L.
author_facet Chaplin, Tristan A.
Hagan, Maureen A.
Allitt, Benjamin J.
Lui, Leo L.
author_sort Chaplin, Tristan A.
collection PubMed
description The study of neuronal responses to random-dot motion patterns has provided some of the most valuable insights into how the activity of neurons is related to perception. In the opposite directions of motion paradigm, the motion signal strength is decreased by manipulating the coherence of random dot patterns to examine how well the activity of single neurons represents the direction of motion. To extend this paradigm to populations of neurons, studies have used modelling based on data from pairs of neurons, but several important questions require further investigation with larger neuronal datasets. We recorded neuronal populations in the middle temporal (MT) and medial superior temporal (MST) areas of anaesthetized marmosets with electrode arrays, while varying the coherence of random dot patterns in two opposite directions of motion (left and right). Using the spike rates of simultaneously recorded neurons, we decoded the direction of motion at each level of coherence with linear classifiers. We found that the presence of correlations had a detrimental effect to decoding performance, but that learning the correlation structure produced better decoding performance compared to decoders that ignored the correlation structure. We also found that reducing motion coherence increased neuronal correlations, but decoders did not need to be optimized for each coherence level. Finally, we showed that decoder weights depend of left-right selectivity at 100% coherence, rather than the preferred direction. These results have implications for understanding how the information encoded by populations of neurons is affected by correlations in spiking activity.
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spelling pubmed-63279412019-01-11 Neuronal Correlations in MT and MST Impair Population Decoding of Opposite Directions of Random Dot Motion Chaplin, Tristan A. Hagan, Maureen A. Allitt, Benjamin J. Lui, Leo L. eNeuro New Research The study of neuronal responses to random-dot motion patterns has provided some of the most valuable insights into how the activity of neurons is related to perception. In the opposite directions of motion paradigm, the motion signal strength is decreased by manipulating the coherence of random dot patterns to examine how well the activity of single neurons represents the direction of motion. To extend this paradigm to populations of neurons, studies have used modelling based on data from pairs of neurons, but several important questions require further investigation with larger neuronal datasets. We recorded neuronal populations in the middle temporal (MT) and medial superior temporal (MST) areas of anaesthetized marmosets with electrode arrays, while varying the coherence of random dot patterns in two opposite directions of motion (left and right). Using the spike rates of simultaneously recorded neurons, we decoded the direction of motion at each level of coherence with linear classifiers. We found that the presence of correlations had a detrimental effect to decoding performance, but that learning the correlation structure produced better decoding performance compared to decoders that ignored the correlation structure. We also found that reducing motion coherence increased neuronal correlations, but decoders did not need to be optimized for each coherence level. Finally, we showed that decoder weights depend of left-right selectivity at 100% coherence, rather than the preferred direction. These results have implications for understanding how the information encoded by populations of neurons is affected by correlations in spiking activity. Society for Neuroscience 2018-01-09 /pmc/articles/PMC6327941/ /pubmed/30637327 http://dx.doi.org/10.1523/ENEURO.0336-18.2018 Text en Copyright © 2018 Chaplin et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Chaplin, Tristan A.
Hagan, Maureen A.
Allitt, Benjamin J.
Lui, Leo L.
Neuronal Correlations in MT and MST Impair Population Decoding of Opposite Directions of Random Dot Motion
title Neuronal Correlations in MT and MST Impair Population Decoding of Opposite Directions of Random Dot Motion
title_full Neuronal Correlations in MT and MST Impair Population Decoding of Opposite Directions of Random Dot Motion
title_fullStr Neuronal Correlations in MT and MST Impair Population Decoding of Opposite Directions of Random Dot Motion
title_full_unstemmed Neuronal Correlations in MT and MST Impair Population Decoding of Opposite Directions of Random Dot Motion
title_short Neuronal Correlations in MT and MST Impair Population Decoding of Opposite Directions of Random Dot Motion
title_sort neuronal correlations in mt and mst impair population decoding of opposite directions of random dot motion
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327941/
https://www.ncbi.nlm.nih.gov/pubmed/30637327
http://dx.doi.org/10.1523/ENEURO.0336-18.2018
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