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Hippocampal memory traces are differentially modulated by experience, time, and adult neurogenesis

机译:海马记忆痕迹受经验,时间和成人神经发生的差异调节

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摘要

Memory traces are believed to be ensembles of cells used to store memories. To visualize memory traces, we created a transgenic line that allows for the comparison between cells activated during encoding and expression of a memory. Mice re-exposed to a fear-inducing context froze more and had a greater percentage of reactivated cells in the dentate gyrus (DG) and CA3 than mice exposed to a novel context. Over time, these differences disappeared, in keeping with the observation that memories become generalized. Optogenetically silencing DG or CA3 cells that were recruited during encoding of a fear-inducing context prevented expression of the corresponding memory. Mice with reduced neurogenesis displayed less contextual memory and less reactivation in CA3but, surprisingly, normal reactivation in the DG. These studies suggest that distinct memory traces are located in the DG and in CA3 but that the strength of the memory is related to reactivation in CA3.
机译:记忆痕迹被认为是用于存储记忆的细胞的集合。为了可视化记忆痕迹,我们创建了一个转基因品系,可以在记忆的编码和表达过程中激活的细胞之间进行比较。与暴露于新环境的小鼠相比,重暴露于诱发恐惧的环境的小鼠更多地冻结,并且在齿状回(DG)和CA3中具有更大百分比的活化细胞。随着时间的流逝,这些差异消失了,这与观察到记忆被普遍化的观察一致。在恐惧诱发背景的编码过程中募集的光遗传沉默DG或CA3细胞阻止了相应记忆的表达。神经发生减少的小鼠在CA3中显示较少的上下文记忆和较少的重新激活,但令人惊讶的是,DG中的正常重新激活。这些研究表明,不同的记忆轨迹位于DG和CA3中,但是记忆的强度与CA3中的重新激活有关。

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