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A Flp-dependent G-CaMP9a transgenic mouse for neuronal imaging in vivo.
Sakamoto, Masayuki; Inoue, Masatoshi; Takeuchi, Atsuya; Kobari, Shigetaka; Yokoyama, Tatsushi; Horigane, Shin-Ichiro; Takemoto-Kimura, Sayaka; Abe, Manabu; Sakimura, Kenji; Kano, Masanobu; Kitamura, Kazuo; Fujii, Hajime; Bito, Haruhiko.
Afiliação
  • Sakamoto M; Department of Neurochemistry, Graduate School of Medicine, The University of Tokyo, Hongo7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
  • Inoue M; Department of Optical Neural and Molecular Physiology, Graduate School of Biostudies, Kyoto University, Kyoto 606-8507, Japan.
  • Takeuchi A; Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency, Kyoto 606-8507, Japan.
  • Kobari S; Department of Neurochemistry, Graduate School of Medicine, The University of Tokyo, Hongo7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
  • Yokoyama T; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.
  • Horigane SI; Department of Neurophysiology, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan.
  • Takemoto-Kimura S; Department of Neurophysiology, School of Dentistry, Tokyo Medical and Dental University, Tokyo, Japan.
  • Abe M; Department of Neurochemistry, Graduate School of Medicine, The University of Tokyo, Hongo7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
  • Sakimura K; Department of Neurochemistry, Graduate School of Medicine, The University of Tokyo, Hongo7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
  • Kano M; Department of Optical Neural and Molecular Physiology, Graduate School of Biostudies, Kyoto University, Kyoto 606-8507, Japan.
  • Kitamura K; Department of Neurochemistry, Graduate School of Medicine, The University of Tokyo, Hongo7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
  • Fujii H; Department of Neuroscience I, Research Institute of Environmental Medicine, Nagoya University, Nagoya, Aichi 464-8602, Japan.
  • Bito H; Department of Molecular/Cellular Neuroscience, Nagoya University Graduate School of Medicine, Nagoya, Aichi 466-8550, Japan.
Cell Rep Methods ; 2(2): 100168, 2022 02 28.
Article em En | MEDLINE | ID: mdl-35474964
ABSTRACT
Genetically encoded calcium indicators (GECIs) are widely used to measure calcium transients in neuronal somata and processes, and their use enables the determination of action potential temporal series in a large population of neurons. Here, we generate a transgenic mouse line expressing a highly sensitive green GECI, G-CaMP9a, in a Flp-dependent manner in excitatory and inhibitory neuronal subpopulations downstream of a strong CAG promoter. Combining this reporter mouse with viral or mouse genetic Flp delivery methods produces a robust and stable G-CaMP9a expression in defined neuronal populations without detectable detrimental effects. In vivo two-photon imaging reveals spontaneous and sensory-evoked calcium transients in excitatory and inhibitory ensembles with cellular resolution. Our results show that this reporter line allows long-term, cell-type-specific investigation of neuronal activity with enhanced resolution in defined populations and facilitates dissecting complex dynamics of neural networks in vivo.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cálcio / Neuroimagem / Neurônios Limite: Animals Idioma: En Revista: Cell Rep Methods Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cálcio / Neuroimagem / Neurônios Limite: Animals Idioma: En Revista: Cell Rep Methods Ano de publicação: 2022 Tipo de documento: Article