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Longitudinal two-photon calcium imaging with ultra-large cranial window for head-fixed mice

Neural activity is heterogeneous across different cortical areas and can change during learning. Here, we describe a protocol for longitudinal in vivo two-photon calcium imaging with an ultra-large cranial window that exposes most of the dorsal cortex in head-fixed mice. The large cranial window all...

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Detalles Bibliográficos
Autores principales: Hattori, Ryoma, Komiyama, Takaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048142/
https://www.ncbi.nlm.nih.gov/pubmed/35496806
http://dx.doi.org/10.1016/j.xpro.2022.101343
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author Hattori, Ryoma
Komiyama, Takaki
author_facet Hattori, Ryoma
Komiyama, Takaki
author_sort Hattori, Ryoma
collection PubMed
description Neural activity is heterogeneous across different cortical areas and can change during learning. Here, we describe a protocol for longitudinal in vivo two-photon calcium imaging with an ultra-large cranial window that exposes most of the dorsal cortex in head-fixed mice. The large cranial window allows optical access to any dorsal cortical areas in individual mice. This protocol enables longitudinal tracking of neural activity from various cortical areas at cellular resolution to understand the cortical computations during behavioral tasks. For complete details on the use and execution of this protocol, please refer to Hattori et al. (2019), and Hattori and Komiyama, 2022a.
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spelling pubmed-90481422022-04-29 Longitudinal two-photon calcium imaging with ultra-large cranial window for head-fixed mice Hattori, Ryoma Komiyama, Takaki STAR Protoc Protocol Neural activity is heterogeneous across different cortical areas and can change during learning. Here, we describe a protocol for longitudinal in vivo two-photon calcium imaging with an ultra-large cranial window that exposes most of the dorsal cortex in head-fixed mice. The large cranial window allows optical access to any dorsal cortical areas in individual mice. This protocol enables longitudinal tracking of neural activity from various cortical areas at cellular resolution to understand the cortical computations during behavioral tasks. For complete details on the use and execution of this protocol, please refer to Hattori et al. (2019), and Hattori and Komiyama, 2022a. Elsevier 2022-04-22 /pmc/articles/PMC9048142/ /pubmed/35496806 http://dx.doi.org/10.1016/j.xpro.2022.101343 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Hattori, Ryoma
Komiyama, Takaki
Longitudinal two-photon calcium imaging with ultra-large cranial window for head-fixed mice
title Longitudinal two-photon calcium imaging with ultra-large cranial window for head-fixed mice
title_full Longitudinal two-photon calcium imaging with ultra-large cranial window for head-fixed mice
title_fullStr Longitudinal two-photon calcium imaging with ultra-large cranial window for head-fixed mice
title_full_unstemmed Longitudinal two-photon calcium imaging with ultra-large cranial window for head-fixed mice
title_short Longitudinal two-photon calcium imaging with ultra-large cranial window for head-fixed mice
title_sort longitudinal two-photon calcium imaging with ultra-large cranial window for head-fixed mice
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048142/
https://www.ncbi.nlm.nih.gov/pubmed/35496806
http://dx.doi.org/10.1016/j.xpro.2022.101343
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