Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Milstein, Aaron D, Li, Yiding, Bittner, Katie C, Grienberger, Christine, Soltesz, Ivan, Magee, Jeffrey C, Romani, Sandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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
_version_ 1784636788432699392
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
work_keys_str_mv AT milsteinaarond bidirectionalsynapticplasticityrapidlymodifieshippocampalrepresentations
AT liyiding bidirectionalsynapticplasticityrapidlymodifieshippocampalrepresentations
AT bittnerkatiec bidirectionalsynapticplasticityrapidlymodifieshippocampalrepresentations
AT grienbergerchristine bidirectionalsynapticplasticityrapidlymodifieshippocampalrepresentations
AT solteszivan bidirectionalsynapticplasticityrapidlymodifieshippocampalrepresentations
AT mageejeffreyc bidirectionalsynapticplasticityrapidlymodifieshippocampalrepresentations
AT romanisandro bidirectionalsynapticplasticityrapidlymodifieshippocampalrepresentations