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Learning and attention increase visual response selectivity through distinct mechanisms
Selectivity of cortical neurons for sensory stimuli can increase across days as animals learn their behavioral relevance and across seconds when animals switch attention. While both phenomena occur in the same circuit, it is unknown whether they rely on similar mechanisms. We imaged primary visual c...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860382/ https://www.ncbi.nlm.nih.gov/pubmed/34906356 http://dx.doi.org/10.1016/j.neuron.2021.11.016 |
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author | Poort, Jasper Wilmes, Katharina A. Blot, Antonin Chadwick, Angus Sahani, Maneesh Clopath, Claudia Mrsic-Flogel, Thomas D. Hofer, Sonja B. Khan, Adil G. |
author_facet | Poort, Jasper Wilmes, Katharina A. Blot, Antonin Chadwick, Angus Sahani, Maneesh Clopath, Claudia Mrsic-Flogel, Thomas D. Hofer, Sonja B. Khan, Adil G. |
author_sort | Poort, Jasper |
collection | PubMed |
description | Selectivity of cortical neurons for sensory stimuli can increase across days as animals learn their behavioral relevance and across seconds when animals switch attention. While both phenomena occur in the same circuit, it is unknown whether they rely on similar mechanisms. We imaged primary visual cortex as mice learned a visual discrimination task and subsequently performed an attention switching task. Selectivity changes due to learning and attention were uncorrelated in individual neurons. Selectivity increases after learning mainly arose from selective suppression of responses to one of the stimuli but from selective enhancement and suppression during attention. Learning and attention differentially affected interactions between excitatory and PV, SOM, and VIP inhibitory cells. Circuit modeling revealed that cell class-specific top-down inputs best explained attentional modulation, while reorganization of local functional connectivity accounted for learning-related changes. Thus, distinct mechanisms underlie increased discriminability of relevant sensory stimuli across longer and shorter timescales. |
format | Online Article Text |
id | pubmed-8860382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-88603822022-02-23 Learning and attention increase visual response selectivity through distinct mechanisms Poort, Jasper Wilmes, Katharina A. Blot, Antonin Chadwick, Angus Sahani, Maneesh Clopath, Claudia Mrsic-Flogel, Thomas D. Hofer, Sonja B. Khan, Adil G. Neuron Article Selectivity of cortical neurons for sensory stimuli can increase across days as animals learn their behavioral relevance and across seconds when animals switch attention. While both phenomena occur in the same circuit, it is unknown whether they rely on similar mechanisms. We imaged primary visual cortex as mice learned a visual discrimination task and subsequently performed an attention switching task. Selectivity changes due to learning and attention were uncorrelated in individual neurons. Selectivity increases after learning mainly arose from selective suppression of responses to one of the stimuli but from selective enhancement and suppression during attention. Learning and attention differentially affected interactions between excitatory and PV, SOM, and VIP inhibitory cells. Circuit modeling revealed that cell class-specific top-down inputs best explained attentional modulation, while reorganization of local functional connectivity accounted for learning-related changes. Thus, distinct mechanisms underlie increased discriminability of relevant sensory stimuli across longer and shorter timescales. Cell Press 2022-02-16 /pmc/articles/PMC8860382/ /pubmed/34906356 http://dx.doi.org/10.1016/j.neuron.2021.11.016 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Poort, Jasper Wilmes, Katharina A. Blot, Antonin Chadwick, Angus Sahani, Maneesh Clopath, Claudia Mrsic-Flogel, Thomas D. Hofer, Sonja B. Khan, Adil G. Learning and attention increase visual response selectivity through distinct mechanisms |
title | Learning and attention increase visual response selectivity through distinct mechanisms |
title_full | Learning and attention increase visual response selectivity through distinct mechanisms |
title_fullStr | Learning and attention increase visual response selectivity through distinct mechanisms |
title_full_unstemmed | Learning and attention increase visual response selectivity through distinct mechanisms |
title_short | Learning and attention increase visual response selectivity through distinct mechanisms |
title_sort | learning and attention increase visual response selectivity through distinct mechanisms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860382/ https://www.ncbi.nlm.nih.gov/pubmed/34906356 http://dx.doi.org/10.1016/j.neuron.2021.11.016 |
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