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Orchestrated experience-driven Arc/Arg3.1 responses are disrupted in a mouse model of Alzheimer’s disease

机译:精心策划的体验驱动的圆弧/ arg3.1响应打乱了阿尔茨海默氏病的小鼠模型

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摘要

Experience-induced expression of immediate-early gene Arc/Arg3.1 is known to play a pivotal role in the consolidation of memory. Here we use in-vivo longitudinal multiphoton imaging to show orchestrated activity-dependent expression of Arc in the mouse extrastriate visual cortex in response to a structured visual stimulation. In wild-type mice, the amplitude of the Arc response in individual neurons strongly predicts the probability of reactivation by a subsequent presentation of the same stimulus. In a mouse model of Alzheimer’s disease, this association is markedly disrupted in the cortex specifically near senile plaques. Neurons in the vicinity of plaques are less likely to respond but, paradoxically, there is stronger response in those few neurons around plaques that do respond. To the extent that the orchestrated pattern of Arc expression reflects nervous system responses to, and physiological consolidation of, behavioral experience, the disruption in Arc patterns reveals plaque-associated interference with neural network integration.
机译:经验诱导的即早基因Arc / Arg3.1的表达在记忆巩固中起关键作用。在这里,我们使用体内纵向多光子成像,以显示响应于结构化视觉刺激的小鼠睾丸外视皮层中精心策划的,依赖于活动的Arc表达。在野生型小鼠中,单个神经元中Arc反应的幅度强烈预测了随后出现的相同刺激而重新激活的可能性。在阿尔茨海默氏病的小鼠模型中,这种关联在皮质中,特别是在老年斑附近,明显被破坏了。斑块附近的神经元反应的可能性较小,但自相矛盾的是,斑块周围的少数确实有反应的神经元的反应较强。在一定程度上,Arc模式的表达模式反映了神经系统对行为体验的反应以及生理上的巩固,Arc模式的破坏揭示了斑块相关的神经网络整合干扰。

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