In utero electroporation and cranial window implantation for in vivo wide-field two-photon calcium imaging using G-CaMP9a transgenic mice

We present a protocol to prepare mouse cranial window implantation for in vivo two-photon wide-field calcium imaging. This protocol uses G-CaMP9a transgenic mice, which express a genetically encoded calcium indicator with high signal-to-noise ratio. We describe in utero electroporation, followed by...

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Bibliographic Details
Published in:STAR protocols 2022-06, Vol.3 (2), p.101421-101421, Article 101421
Main Authors: Sakamoto, Masayuki, Ota, Keisuke, Kondo, Yayoi, Okamura, Michiko, Fujii, Hajime, Bito, Haruhiko
Format: Article
Language:English
Subjects:
Animals
Calcium, Dietary
Developmental biology
Diagnostic Imaging
Electroporation
Mice
Mice, Transgenic
Microscopy
Model Organisms
Neuroscience
Protocol
Skull - surgery
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Summary:We present a protocol to prepare mouse cranial window implantation for in vivo two-photon wide-field calcium imaging. This protocol uses G-CaMP9a transgenic mice, which express a genetically encoded calcium indicator with high signal-to-noise ratio. We describe in utero electroporation, followed by headplate fixation and cranial window implantation. This protocol can be used for measuring neural activity and is suitable for long-term imaging in large populations. Moreover, this protocol does not require preparation of Flp-expressing transgenic mice. For complete details on the use and execution of this protocol, please refer to Sakamoto et al. (2022). [Display omitted] •Preparation of G-CaMP9a knock-in mice for in vivo calcium imaging•In utero electroporation to introduce Flp recombinase in G-CaMP9a mice•Implantation of cranial window for in vivo two-photon calcium imaging Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics. We present a protocol to prepare mouse cranial window implantation for in vivo two-photon wide-field calcium imaging. This protocol uses G-CaMP9a transgenic mice, which express a genetically encoded calcium indicator with high signal-to-noise ratio. We describe in utero electroporation, followed by headplate fixation and cranial window implantation. This protocol can be used for measuring neural activity and is suitable for long-term imaging in large populations. Moreover, this protocol does not require preparation of Flp-expressing transgenic mice.
ISSN:2666-1667
2666-1667
DOI:10.1016/j.xpro.2022.101421