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Model-based analysis of pattern motion processing in mouse primary visual cortex
Neurons in sensory areas of neocortex exhibit responses tuned to specific features of the environment. In visual cortex, information about features such as edges or textures with particular orientations must be integrated to recognize a visual scene or object. Connectivity studies in rodent cortex h...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525018/ https://www.ncbi.nlm.nih.gov/pubmed/26300738 http://dx.doi.org/10.3389/fncir.2015.00038 |
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author | Muir, Dylan R. Roth, Morgane M. Helmchen, Fritjof Kampa, Björn M. |
author_facet | Muir, Dylan R. Roth, Morgane M. Helmchen, Fritjof Kampa, Björn M. |
author_sort | Muir, Dylan R. |
collection | PubMed |
description | Neurons in sensory areas of neocortex exhibit responses tuned to specific features of the environment. In visual cortex, information about features such as edges or textures with particular orientations must be integrated to recognize a visual scene or object. Connectivity studies in rodent cortex have revealed that neurons make specific connections within sub-networks sharing common input tuning. In principle, this sub-network architecture enables local cortical circuits to integrate sensory information. However, whether feature integration indeed occurs locally in rodent primary sensory areas has not been examined directly. We studied local integration of sensory features in primary visual cortex (V1) of the mouse by presenting drifting grating and plaid stimuli, while recording the activity of neuronal populations with two-photon calcium imaging. Using a Bayesian model-based analysis framework, we classified single-cell responses as being selective for either individual grating components or for moving plaid patterns. Rather than relying on trial-averaged responses, our model-based framework takes into account single-trial responses and can easily be extended to consider any number of arbitrary predictive models. Our analysis method was able to successfully classify significantly more responses than traditional partial correlation (PC) analysis, and provides a rigorous statistical framework to rank any number of models and reject poorly performing models. We also found a large proportion of cells that respond strongly to only one stimulus class. In addition, a quarter of selectively responding neurons had more complex responses that could not be explained by any simple integration model. Our results show that a broad range of pattern integration processes already take place at the level of V1. This diversity of integration is consistent with processing of visual inputs by local sub-networks within V1 that are tuned to combinations of sensory features. |
format | Online Article Text |
id | pubmed-4525018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45250182015-08-21 Model-based analysis of pattern motion processing in mouse primary visual cortex Muir, Dylan R. Roth, Morgane M. Helmchen, Fritjof Kampa, Björn M. Front Neural Circuits Neuroscience Neurons in sensory areas of neocortex exhibit responses tuned to specific features of the environment. In visual cortex, information about features such as edges or textures with particular orientations must be integrated to recognize a visual scene or object. Connectivity studies in rodent cortex have revealed that neurons make specific connections within sub-networks sharing common input tuning. In principle, this sub-network architecture enables local cortical circuits to integrate sensory information. However, whether feature integration indeed occurs locally in rodent primary sensory areas has not been examined directly. We studied local integration of sensory features in primary visual cortex (V1) of the mouse by presenting drifting grating and plaid stimuli, while recording the activity of neuronal populations with two-photon calcium imaging. Using a Bayesian model-based analysis framework, we classified single-cell responses as being selective for either individual grating components or for moving plaid patterns. Rather than relying on trial-averaged responses, our model-based framework takes into account single-trial responses and can easily be extended to consider any number of arbitrary predictive models. Our analysis method was able to successfully classify significantly more responses than traditional partial correlation (PC) analysis, and provides a rigorous statistical framework to rank any number of models and reject poorly performing models. We also found a large proportion of cells that respond strongly to only one stimulus class. In addition, a quarter of selectively responding neurons had more complex responses that could not be explained by any simple integration model. Our results show that a broad range of pattern integration processes already take place at the level of V1. This diversity of integration is consistent with processing of visual inputs by local sub-networks within V1 that are tuned to combinations of sensory features. Frontiers Media S.A. 2015-08-05 /pmc/articles/PMC4525018/ /pubmed/26300738 http://dx.doi.org/10.3389/fncir.2015.00038 Text en Copyright © 2015 Muir, Roth, Helmchen and Kampa. 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) 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 Muir, Dylan R. Roth, Morgane M. Helmchen, Fritjof Kampa, Björn M. Model-based analysis of pattern motion processing in mouse primary visual cortex |
title | Model-based analysis of pattern motion processing in mouse primary visual cortex |
title_full | Model-based analysis of pattern motion processing in mouse primary visual cortex |
title_fullStr | Model-based analysis of pattern motion processing in mouse primary visual cortex |
title_full_unstemmed | Model-based analysis of pattern motion processing in mouse primary visual cortex |
title_short | Model-based analysis of pattern motion processing in mouse primary visual cortex |
title_sort | model-based analysis of pattern motion processing in mouse primary visual cortex |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525018/ https://www.ncbi.nlm.nih.gov/pubmed/26300738 http://dx.doi.org/10.3389/fncir.2015.00038 |
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