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.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alzheimer Disease / physiopathology
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Amyloid beta-Protein Precursor / genetics
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Animals
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Brain / drug effects
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Brain / physiology*
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Brain / physiopathology
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Cytoskeletal Proteins / genetics*
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Disease Models, Animal
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Fluorescence
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Green Fluorescent Proteins / genetics*
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Green Fluorescent Proteins / metabolism*
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Humans
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Male
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Mice
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Mice, Transgenic
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Nerve Tissue Proteins / genetics*
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Neurons / drug effects
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Neurons / physiology*
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Presenilin-1 / genetics
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Presenilin-2 / genetics
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Promoter Regions, Genetic
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Protease Nexins
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Receptors, Cell Surface / genetics
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Stress, Physiological / drug effects
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Stress, Physiological / physiology
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Time Factors
Substances
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Amyloid beta-Protein Precursor
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Cytoskeletal Proteins
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Nerve Tissue Proteins
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PSEN1 protein, human
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PSEN2 protein, human
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Presenilin-1
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Presenilin-2
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Protease Nexins
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Receptors, Cell Surface
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activity regulated cytoskeletal-associated protein
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enhanced green fluorescent protein
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Green Fluorescent Proteins