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Contribution of apical and basal dendrites to orientation encoding in mouse V1 L2/3 pyramidal neurons
Pyramidal neurons integrate synaptic inputs from basal and apical dendrites to generate stimulus-specific responses. It has been proposed that feed-forward inputs to basal dendrites drive a neuron’s stimulus preference, while feedback inputs to apical dendrites sharpen selectivity. However, how a ne...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879601/ https://www.ncbi.nlm.nih.gov/pubmed/31772192 http://dx.doi.org/10.1038/s41467-019-13029-0 |
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author | Park, Jiyoung Papoutsi, Athanasia Ash, Ryan T. Marin, Miguel A. Poirazi, Panayiota Smirnakis, Stelios M. |
author_facet | Park, Jiyoung Papoutsi, Athanasia Ash, Ryan T. Marin, Miguel A. Poirazi, Panayiota Smirnakis, Stelios M. |
author_sort | Park, Jiyoung |
collection | PubMed |
description | Pyramidal neurons integrate synaptic inputs from basal and apical dendrites to generate stimulus-specific responses. It has been proposed that feed-forward inputs to basal dendrites drive a neuron’s stimulus preference, while feedback inputs to apical dendrites sharpen selectivity. However, how a neuron’s dendritic domains relate to its functional selectivity has not been demonstrated experimentally. We performed 2-photon dendritic micro-dissection on layer-2/3 pyramidal neurons in mouse primary visual cortex. We found that removing the apical dendritic tuft did not alter orientation-tuning. Furthermore, orientation-tuning curves were remarkably robust to the removal of basal dendrites: ablation of 2 basal dendrites was needed to cause a small shift in orientation preference, without significantly altering tuning width. Computational modeling corroborated our results and put limits on how orientation preferences among basal dendrites differ in order to reproduce the post-ablation data. In conclusion, neuronal orientation-tuning appears remarkably robust to loss of dendritic input. |
format | Online Article Text |
id | pubmed-6879601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68796012019-11-29 Contribution of apical and basal dendrites to orientation encoding in mouse V1 L2/3 pyramidal neurons Park, Jiyoung Papoutsi, Athanasia Ash, Ryan T. Marin, Miguel A. Poirazi, Panayiota Smirnakis, Stelios M. Nat Commun Article Pyramidal neurons integrate synaptic inputs from basal and apical dendrites to generate stimulus-specific responses. It has been proposed that feed-forward inputs to basal dendrites drive a neuron’s stimulus preference, while feedback inputs to apical dendrites sharpen selectivity. However, how a neuron’s dendritic domains relate to its functional selectivity has not been demonstrated experimentally. We performed 2-photon dendritic micro-dissection on layer-2/3 pyramidal neurons in mouse primary visual cortex. We found that removing the apical dendritic tuft did not alter orientation-tuning. Furthermore, orientation-tuning curves were remarkably robust to the removal of basal dendrites: ablation of 2 basal dendrites was needed to cause a small shift in orientation preference, without significantly altering tuning width. Computational modeling corroborated our results and put limits on how orientation preferences among basal dendrites differ in order to reproduce the post-ablation data. In conclusion, neuronal orientation-tuning appears remarkably robust to loss of dendritic input. Nature Publishing Group UK 2019-11-26 /pmc/articles/PMC6879601/ /pubmed/31772192 http://dx.doi.org/10.1038/s41467-019-13029-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Park, Jiyoung Papoutsi, Athanasia Ash, Ryan T. Marin, Miguel A. Poirazi, Panayiota Smirnakis, Stelios M. Contribution of apical and basal dendrites to orientation encoding in mouse V1 L2/3 pyramidal neurons |
title | Contribution of apical and basal dendrites to orientation encoding in mouse V1 L2/3 pyramidal neurons |
title_full | Contribution of apical and basal dendrites to orientation encoding in mouse V1 L2/3 pyramidal neurons |
title_fullStr | Contribution of apical and basal dendrites to orientation encoding in mouse V1 L2/3 pyramidal neurons |
title_full_unstemmed | Contribution of apical and basal dendrites to orientation encoding in mouse V1 L2/3 pyramidal neurons |
title_short | Contribution of apical and basal dendrites to orientation encoding in mouse V1 L2/3 pyramidal neurons |
title_sort | contribution of apical and basal dendrites to orientation encoding in mouse v1 l2/3 pyramidal neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879601/ https://www.ncbi.nlm.nih.gov/pubmed/31772192 http://dx.doi.org/10.1038/s41467-019-13029-0 |
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