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Dendritic Compartmentalization of Learning-Related Plasticity
The dendrites of cortical pyramidal neurons receive synaptic inputs from different pathways that are organized according to their laminar target. This architectural scheme provides cortical neurons with a spatial mechanism to separate information, which may support neural flexibility required during...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233502/ https://www.ncbi.nlm.nih.gov/pubmed/35701166 http://dx.doi.org/10.1523/ENEURO.0060-22.2022 |
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author | Godenzini, Luca Shai, Adam S. Palmer, Lucy M. |
author_facet | Godenzini, Luca Shai, Adam S. Palmer, Lucy M. |
author_sort | Godenzini, Luca |
collection | PubMed |
description | The dendrites of cortical pyramidal neurons receive synaptic inputs from different pathways that are organized according to their laminar target. This architectural scheme provides cortical neurons with a spatial mechanism to separate information, which may support neural flexibility required during learning. Here, we investigated layer-specific plasticity of sensory encoding following learning by recording from two different dendritic compartments, tuft and basal dendrites, of layer 2/3 (L2/3) pyramidal neurons in the auditory cortex of mice. Following auditory fear conditioning, auditory-evoked Ca(2+) responses were enhanced in tuft, but not basal, dendrites leading to increased somatic action potential output. This is in direct contrast to the long held (and debated) hypothesis that, despite extensive dendritic arbors, neurons function as a simple one-compartment model. Two computational models of varying complexity based on the experimental data illustrated that this learning-related increase of auditory responses in tuft dendrites can account for the changes in somatic output. Taken together, we illustrate that neurons do not function as a single compartment, and dendritic compartmentalization of learning-related plasticity may act to increase the computational power of pyramidal neurons. |
format | Online Article Text |
id | pubmed-9233502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-92335022022-06-27 Dendritic Compartmentalization of Learning-Related Plasticity Godenzini, Luca Shai, Adam S. Palmer, Lucy M. eNeuro Research Article: New Research The dendrites of cortical pyramidal neurons receive synaptic inputs from different pathways that are organized according to their laminar target. This architectural scheme provides cortical neurons with a spatial mechanism to separate information, which may support neural flexibility required during learning. Here, we investigated layer-specific plasticity of sensory encoding following learning by recording from two different dendritic compartments, tuft and basal dendrites, of layer 2/3 (L2/3) pyramidal neurons in the auditory cortex of mice. Following auditory fear conditioning, auditory-evoked Ca(2+) responses were enhanced in tuft, but not basal, dendrites leading to increased somatic action potential output. This is in direct contrast to the long held (and debated) hypothesis that, despite extensive dendritic arbors, neurons function as a simple one-compartment model. Two computational models of varying complexity based on the experimental data illustrated that this learning-related increase of auditory responses in tuft dendrites can account for the changes in somatic output. Taken together, we illustrate that neurons do not function as a single compartment, and dendritic compartmentalization of learning-related plasticity may act to increase the computational power of pyramidal neurons. Society for Neuroscience 2022-06-22 /pmc/articles/PMC9233502/ /pubmed/35701166 http://dx.doi.org/10.1523/ENEURO.0060-22.2022 Text en Copyright © 2022 Godenzini et al. https://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 (https://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 | Research Article: New Research Godenzini, Luca Shai, Adam S. Palmer, Lucy M. Dendritic Compartmentalization of Learning-Related Plasticity |
title | Dendritic Compartmentalization of Learning-Related Plasticity |
title_full | Dendritic Compartmentalization of Learning-Related Plasticity |
title_fullStr | Dendritic Compartmentalization of Learning-Related Plasticity |
title_full_unstemmed | Dendritic Compartmentalization of Learning-Related Plasticity |
title_short | Dendritic Compartmentalization of Learning-Related Plasticity |
title_sort | dendritic compartmentalization of learning-related plasticity |
topic | Research Article: New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233502/ https://www.ncbi.nlm.nih.gov/pubmed/35701166 http://dx.doi.org/10.1523/ENEURO.0060-22.2022 |
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