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Presynaptic supervision of cortical spine dynamics in motor learning
In mammalian neocortex, learning triggers the formation and turnover of new postsynaptic spines on pyramidal cell dendrites. However, the biological principles of spine reorganization during learning remain elusive because the identity of their presynaptic neuronal partners is unknown. Here, we show...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328689/ https://www.ncbi.nlm.nih.gov/pubmed/35895812 http://dx.doi.org/10.1126/sciadv.abm0531 |
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author | Sohn, Jaerin Suzuki, Mototaka Youssef, Mohammed Hatada, Sayuri Larkum, Matthew E. Kawaguchi, Yasuo Kubota, Yoshiyuki |
author_facet | Sohn, Jaerin Suzuki, Mototaka Youssef, Mohammed Hatada, Sayuri Larkum, Matthew E. Kawaguchi, Yasuo Kubota, Yoshiyuki |
author_sort | Sohn, Jaerin |
collection | PubMed |
description | In mammalian neocortex, learning triggers the formation and turnover of new postsynaptic spines on pyramidal cell dendrites. However, the biological principles of spine reorganization during learning remain elusive because the identity of their presynaptic neuronal partners is unknown. Here, we show that two presynaptic neural circuits supervise distinct programs of spine dynamics to execute learning. We imaged spine dynamics in motor cortex during learning and performed post hoc identification of their afferent presynaptic neurons. New spines that appeared during learning formed small transient contacts with corticocortical neurons that were eliminated on skill acquisition. In contrast, persistent spines with axons from thalamic neurons were formed and enlarged. These results suggest that pyramidal cell dendrites in motor cortex use a neural circuit division of labor during skill learning, with dynamic teaching contacts from top-down intracortical axons followed by synaptic memory formation driven by thalamic axons. Dual spine supervision may govern diverse skill learning in the neocortex. |
format | Online Article Text |
id | pubmed-9328689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-93286892022-08-09 Presynaptic supervision of cortical spine dynamics in motor learning Sohn, Jaerin Suzuki, Mototaka Youssef, Mohammed Hatada, Sayuri Larkum, Matthew E. Kawaguchi, Yasuo Kubota, Yoshiyuki Sci Adv Neuroscience In mammalian neocortex, learning triggers the formation and turnover of new postsynaptic spines on pyramidal cell dendrites. However, the biological principles of spine reorganization during learning remain elusive because the identity of their presynaptic neuronal partners is unknown. Here, we show that two presynaptic neural circuits supervise distinct programs of spine dynamics to execute learning. We imaged spine dynamics in motor cortex during learning and performed post hoc identification of their afferent presynaptic neurons. New spines that appeared during learning formed small transient contacts with corticocortical neurons that were eliminated on skill acquisition. In contrast, persistent spines with axons from thalamic neurons were formed and enlarged. These results suggest that pyramidal cell dendrites in motor cortex use a neural circuit division of labor during skill learning, with dynamic teaching contacts from top-down intracortical axons followed by synaptic memory formation driven by thalamic axons. Dual spine supervision may govern diverse skill learning in the neocortex. American Association for the Advancement of Science 2022-07-27 /pmc/articles/PMC9328689/ /pubmed/35895812 http://dx.doi.org/10.1126/sciadv.abm0531 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Neuroscience Sohn, Jaerin Suzuki, Mototaka Youssef, Mohammed Hatada, Sayuri Larkum, Matthew E. Kawaguchi, Yasuo Kubota, Yoshiyuki Presynaptic supervision of cortical spine dynamics in motor learning |
title | Presynaptic supervision of cortical spine dynamics in motor learning |
title_full | Presynaptic supervision of cortical spine dynamics in motor learning |
title_fullStr | Presynaptic supervision of cortical spine dynamics in motor learning |
title_full_unstemmed | Presynaptic supervision of cortical spine dynamics in motor learning |
title_short | Presynaptic supervision of cortical spine dynamics in motor learning |
title_sort | presynaptic supervision of cortical spine dynamics in motor learning |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328689/ https://www.ncbi.nlm.nih.gov/pubmed/35895812 http://dx.doi.org/10.1126/sciadv.abm0531 |
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