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Bidirectional synaptic plasticity rapidly modifies hippocampal representations
Learning requires neural adaptations thought to be mediated by activity-dependent synaptic plasticity. A relatively non-standard form of synaptic plasticity driven by dendritic calcium spikes, or plateau potentials, has been reported to underlie place field formation in rodent hippocampal CA1 neuron...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776257/ https://www.ncbi.nlm.nih.gov/pubmed/34882093 http://dx.doi.org/10.7554/eLife.73046 |
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author | Milstein, Aaron D Li, Yiding Bittner, Katie C Grienberger, Christine Soltesz, Ivan Magee, Jeffrey C Romani, Sandro |
author_facet | Milstein, Aaron D Li, Yiding Bittner, Katie C Grienberger, Christine Soltesz, Ivan Magee, Jeffrey C Romani, Sandro |
author_sort | Milstein, Aaron D |
collection | PubMed |
description | Learning requires neural adaptations thought to be mediated by activity-dependent synaptic plasticity. A relatively non-standard form of synaptic plasticity driven by dendritic calcium spikes, or plateau potentials, has been reported to underlie place field formation in rodent hippocampal CA1 neurons. Here, we found that this behavioral timescale synaptic plasticity (BTSP) can also reshape existing place fields via bidirectional synaptic weight changes that depend on the temporal proximity of plateau potentials to pre-existing place fields. When evoked near an existing place field, plateau potentials induced less synaptic potentiation and more depression, suggesting BTSP might depend inversely on postsynaptic activation. However, manipulations of place cell membrane potential and computational modeling indicated that this anti-correlation actually results from a dependence on current synaptic weight such that weak inputs potentiate and strong inputs depress. A network model implementing this bidirectional synaptic learning rule suggested that BTSP enables population activity, rather than pairwise neuronal correlations, to drive neural adaptations to experience. |
format | Online Article Text |
id | pubmed-8776257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-87762572022-01-21 Bidirectional synaptic plasticity rapidly modifies hippocampal representations Milstein, Aaron D Li, Yiding Bittner, Katie C Grienberger, Christine Soltesz, Ivan Magee, Jeffrey C Romani, Sandro eLife Neuroscience Learning requires neural adaptations thought to be mediated by activity-dependent synaptic plasticity. A relatively non-standard form of synaptic plasticity driven by dendritic calcium spikes, or plateau potentials, has been reported to underlie place field formation in rodent hippocampal CA1 neurons. Here, we found that this behavioral timescale synaptic plasticity (BTSP) can also reshape existing place fields via bidirectional synaptic weight changes that depend on the temporal proximity of plateau potentials to pre-existing place fields. When evoked near an existing place field, plateau potentials induced less synaptic potentiation and more depression, suggesting BTSP might depend inversely on postsynaptic activation. However, manipulations of place cell membrane potential and computational modeling indicated that this anti-correlation actually results from a dependence on current synaptic weight such that weak inputs potentiate and strong inputs depress. A network model implementing this bidirectional synaptic learning rule suggested that BTSP enables population activity, rather than pairwise neuronal correlations, to drive neural adaptations to experience. eLife Sciences Publications, Ltd 2021-12-09 /pmc/articles/PMC8776257/ /pubmed/34882093 http://dx.doi.org/10.7554/eLife.73046 Text en © 2021, Milstein et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Milstein, Aaron D Li, Yiding Bittner, Katie C Grienberger, Christine Soltesz, Ivan Magee, Jeffrey C Romani, Sandro Bidirectional synaptic plasticity rapidly modifies hippocampal representations |
title | Bidirectional synaptic plasticity rapidly modifies hippocampal representations |
title_full | Bidirectional synaptic plasticity rapidly modifies hippocampal representations |
title_fullStr | Bidirectional synaptic plasticity rapidly modifies hippocampal representations |
title_full_unstemmed | Bidirectional synaptic plasticity rapidly modifies hippocampal representations |
title_short | Bidirectional synaptic plasticity rapidly modifies hippocampal representations |
title_sort | bidirectional synaptic plasticity rapidly modifies hippocampal representations |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776257/ https://www.ncbi.nlm.nih.gov/pubmed/34882093 http://dx.doi.org/10.7554/eLife.73046 |
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