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

Summary: 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 w...

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Main Authors: Ryoma Hattori, Takaki Komiyama
Format: Article
Language:English
Published: Elsevier 2022-06-01
Series:STAR Protocols
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666166722002234
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author Ryoma Hattori
Takaki Komiyama
author_facet Ryoma Hattori
Takaki Komiyama
author_sort Ryoma Hattori
collection DOAJ
description Summary: 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 doaj.art-ca19f2eab20d4875841c4ad0c1020ee32022-12-22T02:24:21ZengElsevierSTAR Protocols2666-16672022-06-0132101343Longitudinal two-photon calcium imaging with ultra-large cranial window for head-fixed miceRyoma Hattori0Takaki Komiyama1Neurobiology Section, Center for Neural Circuits and Behavior, Department of Neurosciences, and Halıcıoğlu Data Science Institute, University of California, San Diego, La Jolla, CA 92093, USA; Corresponding authorNeurobiology Section, Center for Neural Circuits and Behavior, Department of Neurosciences, and Halıcıoğlu Data Science Institute, University of California, San Diego, La Jolla, CA 92093, USA; Corresponding authorSummary: 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.http://www.sciencedirect.com/science/article/pii/S2666166722002234MicroscopyModel OrganismsNeuroscience
spellingShingle Ryoma Hattori
Takaki Komiyama
Longitudinal two-photon calcium imaging with ultra-large cranial window for head-fixed mice
STAR Protocols
Microscopy
Model Organisms
Neuroscience
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 Microscopy
Model Organisms
Neuroscience
url http://www.sciencedirect.com/science/article/pii/S2666166722002234
work_keys_str_mv AT ryomahattori longitudinaltwophotoncalciumimagingwithultralargecranialwindowforheadfixedmice
AT takakikomiyama longitudinaltwophotoncalciumimagingwithultralargecranialwindowforheadfixedmice