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并非所有的 IEGs 都是平等的——记忆印痕中的分子分类。

All IEGs Are Not Created Equal-Molecular Sorting Within the Memory Engram.

机构信息

Department of Psychiatry, O'Donnell Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Neuroscience Graduate Program, University of Texas Southwestern Medical Center, Dallas, TX, USA.

出版信息

Adv Neurobiol. 2024;38:81-109. doi: 10.1007/978-3-031-62983-9_6.

Abstract

When neurons are recruited to form the memory engram, they are driven to activate the expression of a series of immediate-early genes (IEGs). While these IEGs have been used relatively indiscriminately to identify the so-called engram neurons, recent research has demonstrated that different IEG ensembles can be physically and functionally distinct within the memory engram. This inherent heterogeneity of the memory engram is driven by the diversity in the functions and distributions of different IEGs. This process, which we call molecular sorting, is analogous to sorting the entire population of engram neurons into different sub-engrams molecularly defined by different IEGs. In this chapter, we will describe the molecular sorting process by systematically reviewing published work on engram ensemble cells defined by the following four major IEGs: Fos, Npas4, Arc, and Egr1. By comparing and contrasting these likely different components of the memory engram, we hope to gain a better understanding of the logic and significance behind the molecular sorting process for memory functions.

摘要

当神经元被招募来形成记忆痕迹时,它们会被驱动去激活一系列即时早期基因(IEGs)的表达。虽然这些 IEG 被相对不加区分地用于识别所谓的记忆痕迹神经元,但最近的研究表明,不同的 IEG 集合在记忆痕迹中可以在物理和功能上有所不同。记忆痕迹的这种内在异质性是由不同 IEG 的功能和分布多样性所驱动的。这个过程,我们称之为分子分拣,类似于将整个记忆痕迹神经元群体按照不同的 IEG 分子定义的不同子记忆痕迹进行分拣。在本章中,我们将通过系统地回顾以下四个主要的 IEG(Fos、Npas4、Arc 和 Egr1)定义的记忆痕迹集合细胞的已发表工作,来描述分子分拣过程。通过比较和对比这些记忆痕迹的可能不同组成部分,我们希望更好地理解记忆功能的分子分拣过程背后的逻辑和意义。

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