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Fluorescent Arc/Arg3.1 indicator mice: a versatile tool to study brain activity changes in vitro and in vivo

MPS-Authors
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Grinevich,  Valery
Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society;

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Kolleker,  Aleksandre
Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society;

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Eliava,  Marina
Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society;

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Takuma,  Hiroshi
Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society;

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Waters,  David Jack
Department of Cell Physiology, Max Planck Institute for Medical Research, Max Planck Society;

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Seeburg,  Peter H.
Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society;

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Osten,  Pavel
Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society;

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Citation

Grinevich, V., Kolleker, A., Eliava, M., Takada, N., Takuma, H., Fukuzawa, Y., et al. (2009). Fluorescent Arc/Arg3.1 indicator mice: a versatile tool to study brain activity changes in vitro and in vivo. Journal of Neuroscience Methods, 184(1), 25-26. doi:10.1016/j.jneumeth.2009.07.015.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002C-110B-3
Abstract
The brain-specific immediate early gene Arc/Arg3.1 is induced in response to a variety of stimuli, including sensory and behavior-linked neural activity. Here we report the generation of transgenic mice, termed TgArc/Arg3.1-d4EGFP, expressing a 4-h half-life form of enhanced green fluorescent protein (d4EGFP) under the control of the Arc/Arg3.1 promoter. We show that d4EGFP-mediated fluorescence faithfully reports Arc/Arg3.1 induction in response to physiological, pathological and pharmacological stimuli, and that this fluorescence permits electrical recording from activated neurons in the live mouse. Moreover, the fluorescent Arc/Arg3.1 indicator revealed activity changes in circumscribed brain areas in distinct modes of stress and in a mouse model of Alzheimer's disease. These findings identify the TgArc/Arg3.1-d4EGFP mouse as a versatile tool to monitor Arc/Arg3.1 induction in neural circuits, both in vitro and in vivo.