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All-optical physiology resolves a synaptic basis for behavioral timescale plasticity

Learning has been associated with modifications of synaptic and circuit properties, but the precise changes storing information in mammals have remained largely unclear. We combined genetically targeted voltage imaging with targeted optogenetic activation and silencing of pre- and post-synaptic neur...

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Autores principales: Fan, Linlin Z., Kim, Doo Kyung, Jennings, Joshua H., Tian, He, Wang, Peter Y., Ramakrishnan, Charu, Randles, Sawyer, Sun, Yanjun, Thadhani, Elina, Kim, Yoon Seok, Quirin, Sean, Giocomo, Lisa, Cohen, Adam E., Deisseroth, Karl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327443/
https://www.ncbi.nlm.nih.gov/pubmed/36669484
http://dx.doi.org/10.1016/j.cell.2022.12.035
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author Fan, Linlin Z.
Kim, Doo Kyung
Jennings, Joshua H.
Tian, He
Wang, Peter Y.
Ramakrishnan, Charu
Randles, Sawyer
Sun, Yanjun
Thadhani, Elina
Kim, Yoon Seok
Quirin, Sean
Giocomo, Lisa
Cohen, Adam E.
Deisseroth, Karl
author_facet Fan, Linlin Z.
Kim, Doo Kyung
Jennings, Joshua H.
Tian, He
Wang, Peter Y.
Ramakrishnan, Charu
Randles, Sawyer
Sun, Yanjun
Thadhani, Elina
Kim, Yoon Seok
Quirin, Sean
Giocomo, Lisa
Cohen, Adam E.
Deisseroth, Karl
author_sort Fan, Linlin Z.
collection PubMed
description Learning has been associated with modifications of synaptic and circuit properties, but the precise changes storing information in mammals have remained largely unclear. We combined genetically targeted voltage imaging with targeted optogenetic activation and silencing of pre- and post-synaptic neurons to study the mechanisms underlying hippocampal behavioral timescale plasticity. In mice navigating a virtual-reality environment, targeted optogenetic activation of individual CA1 cells at specific places induced stable representations of these places in the targeted cells. Optical elicitation, recording, and modulation of synaptic transmission in behaving mice revealed that activity in presynaptic CA2/3 cells was required for the induction of plasticity in CA1 and, furthermore, that during induction of these place fields in single CA1 cells, synaptic input from CA2/3 onto these same cells was potentiated. These results reveal synaptic implementation of hippocampal behavioral timescale plasticity and define a methodology to resolve synaptic plasticity during learning and memory in behaving mammals.
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spelling pubmed-103274432023-07-07 All-optical physiology resolves a synaptic basis for behavioral timescale plasticity Fan, Linlin Z. Kim, Doo Kyung Jennings, Joshua H. Tian, He Wang, Peter Y. Ramakrishnan, Charu Randles, Sawyer Sun, Yanjun Thadhani, Elina Kim, Yoon Seok Quirin, Sean Giocomo, Lisa Cohen, Adam E. Deisseroth, Karl Cell Article Learning has been associated with modifications of synaptic and circuit properties, but the precise changes storing information in mammals have remained largely unclear. We combined genetically targeted voltage imaging with targeted optogenetic activation and silencing of pre- and post-synaptic neurons to study the mechanisms underlying hippocampal behavioral timescale plasticity. In mice navigating a virtual-reality environment, targeted optogenetic activation of individual CA1 cells at specific places induced stable representations of these places in the targeted cells. Optical elicitation, recording, and modulation of synaptic transmission in behaving mice revealed that activity in presynaptic CA2/3 cells was required for the induction of plasticity in CA1 and, furthermore, that during induction of these place fields in single CA1 cells, synaptic input from CA2/3 onto these same cells was potentiated. These results reveal synaptic implementation of hippocampal behavioral timescale plasticity and define a methodology to resolve synaptic plasticity during learning and memory in behaving mammals. 2023-02-02 2023-01-19 /pmc/articles/PMC10327443/ /pubmed/36669484 http://dx.doi.org/10.1016/j.cell.2022.12.035 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License, which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Fan, Linlin Z.
Kim, Doo Kyung
Jennings, Joshua H.
Tian, He
Wang, Peter Y.
Ramakrishnan, Charu
Randles, Sawyer
Sun, Yanjun
Thadhani, Elina
Kim, Yoon Seok
Quirin, Sean
Giocomo, Lisa
Cohen, Adam E.
Deisseroth, Karl
All-optical physiology resolves a synaptic basis for behavioral timescale plasticity
title All-optical physiology resolves a synaptic basis for behavioral timescale plasticity
title_full All-optical physiology resolves a synaptic basis for behavioral timescale plasticity
title_fullStr All-optical physiology resolves a synaptic basis for behavioral timescale plasticity
title_full_unstemmed All-optical physiology resolves a synaptic basis for behavioral timescale plasticity
title_short All-optical physiology resolves a synaptic basis for behavioral timescale plasticity
title_sort all-optical physiology resolves a synaptic basis for behavioral timescale plasticity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327443/
https://www.ncbi.nlm.nih.gov/pubmed/36669484
http://dx.doi.org/10.1016/j.cell.2022.12.035
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