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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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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. |
format | Online Article Text |
id | pubmed-10327443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
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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