IF 14.7 1区 医学 Q1 NEUROSCIENCES
Bo Lei, Bilin Kang, Yuejun Hao, Haoyu Yang, Zihan Zhong, Zihan Zhai, Yi Zhong
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引用次数: 0

摘要

在一个被称为系统再巩固的过程中,唤起系统巩固的新皮质依赖性远程记忆会重新激活海马体。然而,其潜在的机制,尤其是恢复的海马记忆刻痕的起源,仍然难以捉摸。通过开发一种三重事件标记工具并利用双光子成像技术,我们追踪了从记忆获得到系统再巩固的海马记忆组合,并发现远程回忆会在海马中招募一个新的记忆组合,用于随后的记忆检索。成年海马神经发生介导的对原始记忆的沉默支持了新记忆组的招募。这种新的记忆片段组合接收当前经历过的情境信息,将新信息纳入远程记忆,并支持远程记忆更新。然后,通过内侧前额叶皮层投射介导的海马和杏仁核之间的活动协调,这种重建的海马记忆会与遥远记忆的价值相整合。因此,新记忆片段的重建是系统再巩固的基础,而系统再巩固则解释了遥远记忆是如何被新信息更新的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reconstructing a new hippocampal engram for systems reconsolidation and remote memory updating.

Recalling systems-consolidated neocortex-dependent remote memories re-engages the hippocampus in a process called systems reconsolidation. However, underlying mechanisms, particularly for the origin of the reinstated hippocampal memory engram, remain elusive. By developing a triple-event labeling tool and employing two-photon imaging, we trace hippocampal engram ensembles from memory acquisition to systems reconsolidation and find that remote recall recruits a new engram ensemble in the hippocampus for subsequent memory retrieval. Consistently, recruiting new engrams is supported by adult hippocampal neurogenesis-mediated silencing of original engrams. This new engram ensemble receives currently experienced contextual information, incorporates new information into the remote memory, and supports remote memory updating. Such a reconstructed hippocampal memory is then integrated with the valence of remote memory via medial prefrontal cortex projection-mediated activity coordination between the hippocampus and amygdala. Thus, the reconstruction of new memory engrams underlies systems reconsolidation, which explains how remote memories are updated with new information.

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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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