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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...

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Autores principales: Sohn, Jaerin, Suzuki, Mototaka, Youssef, Mohammed, Hatada, Sayuri, Larkum, Matthew E., Kawaguchi, Yasuo, Kubota, Yoshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
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.
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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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