Department of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA; Department of Molecular Neurobiology, Max-Planck-Institute for Medical Research, D-69120 Heidelberg, Germany.
J Neurosci Methods. 2009 Oct 30;184(1):25-36. doi: 10.1016/j.jneumeth.2009.07.015. Epub 2009 Jul 21.
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.
大脑特异性即时早期基因 Arc/Arg3.1 可响应各种刺激(包括感觉和与行为相关的神经活动)而被诱导。在这里,我们报告了一种转基因小鼠的产生,称为 TgArc/Arg3.1-d4EGFP,其在 Arc/Arg3.1 启动子的控制下表达具有 4 小时半衰期的增强型绿色荧光蛋白(d4EGFP)。我们表明,d4EGFP 介导的荧光忠实地报告了响应生理、病理和药理学刺激的 Arc/Arg3.1 诱导,并且这种荧光允许从活体小鼠中的激活神经元进行电记录。此外,荧光 Arc/Arg3.1 指示剂揭示了在不同应激模式和阿尔茨海默病小鼠模型中的特定脑区中的活性变化。这些发现确定了 TgArc/Arg3.1-d4EGFP 小鼠作为在体外和体内监测神经回路中 Arc/Arg3.1 诱导的多功能工具。