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Induction of input-specific spine shrinkage on dendrites of rodent hippocampal CA1 neurons using two-photon glutamate uncaging

Shrinkage and loss of dendritic spines are vital components of the neuronal plasticity that supports learning. To investigate the mechanisms of spine shrinkage and loss, Oh and colleagues established a two-photon glutamate uncaging protocol that reliably induces input-specific spine shrinkage on den...

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Detalles Bibliográficos
Autores principales: Jang, Jinyoung, Anisimova, Margarita, Oh, Won Chan, Zito, Karen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672044/
https://www.ncbi.nlm.nih.gov/pubmed/34950882
http://dx.doi.org/10.1016/j.xpro.2021.100996
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author Jang, Jinyoung
Anisimova, Margarita
Oh, Won Chan
Zito, Karen
author_facet Jang, Jinyoung
Anisimova, Margarita
Oh, Won Chan
Zito, Karen
author_sort Jang, Jinyoung
collection PubMed
description Shrinkage and loss of dendritic spines are vital components of the neuronal plasticity that supports learning. To investigate the mechanisms of spine shrinkage and loss, Oh and colleagues established a two-photon glutamate uncaging protocol that reliably induces input-specific spine shrinkage on dendrites of rodent hippocampal CA1 pyramidal neurons. Here, we provide a detailed description of that protocol and also an optimized version that can be used to induce input- and synapse-specific shrinkage of dendritic spines at physiological Ca(2+) levels. For complete details on the use and execution of this protocol, please refer to Oh et al. (2013), Stein et al. (2015), Stein et al. (2020), and Stein et al. (2021).
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spelling pubmed-86720442021-12-22 Induction of input-specific spine shrinkage on dendrites of rodent hippocampal CA1 neurons using two-photon glutamate uncaging Jang, Jinyoung Anisimova, Margarita Oh, Won Chan Zito, Karen STAR Protoc Protocol Shrinkage and loss of dendritic spines are vital components of the neuronal plasticity that supports learning. To investigate the mechanisms of spine shrinkage and loss, Oh and colleagues established a two-photon glutamate uncaging protocol that reliably induces input-specific spine shrinkage on dendrites of rodent hippocampal CA1 pyramidal neurons. Here, we provide a detailed description of that protocol and also an optimized version that can be used to induce input- and synapse-specific shrinkage of dendritic spines at physiological Ca(2+) levels. For complete details on the use and execution of this protocol, please refer to Oh et al. (2013), Stein et al. (2015), Stein et al. (2020), and Stein et al. (2021). Elsevier 2021-12-11 /pmc/articles/PMC8672044/ /pubmed/34950882 http://dx.doi.org/10.1016/j.xpro.2021.100996 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Jang, Jinyoung
Anisimova, Margarita
Oh, Won Chan
Zito, Karen
Induction of input-specific spine shrinkage on dendrites of rodent hippocampal CA1 neurons using two-photon glutamate uncaging
title Induction of input-specific spine shrinkage on dendrites of rodent hippocampal CA1 neurons using two-photon glutamate uncaging
title_full Induction of input-specific spine shrinkage on dendrites of rodent hippocampal CA1 neurons using two-photon glutamate uncaging
title_fullStr Induction of input-specific spine shrinkage on dendrites of rodent hippocampal CA1 neurons using two-photon glutamate uncaging
title_full_unstemmed Induction of input-specific spine shrinkage on dendrites of rodent hippocampal CA1 neurons using two-photon glutamate uncaging
title_short Induction of input-specific spine shrinkage on dendrites of rodent hippocampal CA1 neurons using two-photon glutamate uncaging
title_sort induction of input-specific spine shrinkage on dendrites of rodent hippocampal ca1 neurons using two-photon glutamate uncaging
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672044/
https://www.ncbi.nlm.nih.gov/pubmed/34950882
http://dx.doi.org/10.1016/j.xpro.2021.100996
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