• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

揭示记忆形成和稳定的关键:内嗅皮层颗粒细胞中的转录和表观遗传机制。

Unveiling Transcriptional and Epigenetic Mechanisms Within Engram Cells: Insights into Memory Formation and Stability.

机构信息

Instituto de Neurociencias, Universidad Miguel Hernández - Consejo Superior de Investigaciones Científicas, Alicante, Spain.

出版信息

Adv Neurobiol. 2024;38:111-129. doi: 10.1007/978-3-031-62983-9_7.

DOI:10.1007/978-3-031-62983-9_7
PMID:39008013
Abstract

Memory traces for behavioral experiences, such as fear conditioning or taste aversion, are believed to be stored through biophysical and molecular changes in distributed neuronal ensembles across various brain regions. These ensembles are known as engrams, and the cells that constitute them are referred to as engram cells. Recent advancements in techniques for labeling and manipulating neural activity have facilitated the study of engram cells throughout different memory phases, including acquisition, allocation, long-term storage, retrieval, and erasure. In this chapter, we will explore the application of next-generation sequencing methods to engram research, shedding new light on the contribution of transcriptional and epigenetic mechanisms to engram formation and stability.

摘要

行为经验的记忆痕迹,如恐惧条件反射或味觉厌恶,被认为是通过分布在不同大脑区域的神经元集合中的生物物理和分子变化来存储的。这些集合被称为记忆痕迹,构成它们的细胞被称为记忆痕迹细胞。用于标记和操纵神经活动的新技术的最新进展促进了对整个不同记忆阶段的记忆痕迹细胞的研究,包括获取、分配、长期储存、检索和擦除。在本章中,我们将探讨下一代测序方法在记忆痕迹研究中的应用,为转录和表观遗传机制对记忆痕迹形成和稳定性的贡献提供新的认识。

相似文献

1
Unveiling Transcriptional and Epigenetic Mechanisms Within Engram Cells: Insights into Memory Formation and Stability.揭示记忆形成和稳定的关键:内嗅皮层颗粒细胞中的转录和表观遗传机制。
Adv Neurobiol. 2024;38:111-129. doi: 10.1007/978-3-031-62983-9_7.
2
Brain-wide mapping reveals that engrams for a single memory are distributed across multiple brain regions.全脑图谱揭示,单一记忆的记忆痕迹分布于多个脑区。
Nat Commun. 2022 Apr 4;13(1):1799. doi: 10.1038/s41467-022-29384-4.
3
Memory Storage in Distributed Engram Cell Ensembles.分布式记忆单元集合中的记忆存储
Adv Neurobiol. 2024;38:29-43. doi: 10.1007/978-3-031-62983-9_3.
4
Neuronal ensemble-specific DNA methylation strengthens engram stability.神经元集合特异性 DNA 甲基化增强了印痕稳定性。
Nat Commun. 2020 Jan 31;11(1):639. doi: 10.1038/s41467-020-14498-4.
5
Roles and Transcriptional Responses of Inhibitory Neurons in Learning and Memory.抑制性神经元在学习与记忆中的作用及转录反应
Front Mol Neurosci. 2021 Jun 15;14:689952. doi: 10.3389/fnmol.2021.689952. eCollection 2021.
6
An update on memory formation and retrieval: An engram-centric approach.记忆形成和提取的最新研究进展:以记忆印痕为中心的研究方法。
Alzheimers Dement. 2020 Jun;16(6):926-937. doi: 10.1002/alz.12071. Epub 2020 Apr 25.
7
Excitability mediates allocation of pre-configured ensembles to a hippocampal engram supporting contextual conditioned threat in mice.兴奋性介导预先配置的神经元集群分配至支持小鼠情境性条件性威胁的海马记忆印迹中。
Neuron. 2024 May 1;112(9):1487-1497.e6. doi: 10.1016/j.neuron.2024.02.007. Epub 2024 Mar 5.
8
Parvalbumin interneurons constrain the size of the lateral amygdala engram.小白蛋白中间神经元限制了外侧杏仁核记忆痕迹的大小。
Neurobiol Learn Mem. 2016 Nov;135:91-99. doi: 10.1016/j.nlm.2016.07.007. Epub 2016 Jul 12.
9
Anterior basolateral amygdala neurons comprise a remote fear memory engram.前基底外侧杏仁核神经元构成了遥远的恐惧记忆的印痕。
Front Neural Circuits. 2023 Apr 27;17:1167825. doi: 10.3389/fncir.2023.1167825. eCollection 2023.
10
Functionally Distinct Neuronal Ensembles within the Memory Engram.记忆印迹中的功能独特神经元集合。
Cell. 2020 Apr 16;181(2):410-423.e17. doi: 10.1016/j.cell.2020.02.055. Epub 2020 Mar 17.

引用本文的文献

1
Combinative Protein Expression of Immediate Early Genes c-Fos, Arc, and Npas4 Along Aversive and Appetitive Experience-Related Neural Networks.即刻早期基因c-Fos、Arc和Npas4在厌恶和奖赏相关神经网络中的联合蛋白表达
Hippocampus. 2025 Sep;35(5):e70030. doi: 10.1002/hipo.70030.
2
Combinative protein expression of immediate early genes c-Fos, Arc, and Npas4 along aversive- and reward-related neural networks.即刻早期基因c-Fos、Arc和Npas4在厌恶相关和奖赏相关神经网络中的联合蛋白表达。
bioRxiv. 2025 May 22:2025.04.21.649441. doi: 10.1101/2025.04.21.649441.

本文引用的文献

1
How engram mediates learning, extinction, and relapse.记忆痕迹如何介导学习、遗忘和复发。
Curr Opin Neurobiol. 2023 Aug;81:102723. doi: 10.1016/j.conb.2023.102723. Epub 2023 Apr 6.
2
Hippocampal cells segregate positive and negative engrams.海马体神经元将正、负记忆分开储存。
Commun Biol. 2022 Sep 26;5(1):1009. doi: 10.1038/s42003-022-03906-8.
3
Brain-wide mapping reveals that engrams for a single memory are distributed across multiple brain regions.全脑图谱揭示,单一记忆的记忆痕迹分布于多个脑区。
Nat Commun. 2022 Apr 4;13(1):1799. doi: 10.1038/s41467-022-29384-4.
4
Understanding the physical basis of memory: Molecular mechanisms of the engram.理解记忆的物质基础:记忆的分子机制。
J Biol Chem. 2022 May;298(5):101866. doi: 10.1016/j.jbc.2022.101866. Epub 2022 Mar 26.
5
Forgetting as a form of adaptive engram cell plasticity.遗忘作为一种适应性的记忆痕迹细胞可塑性形式。
Nat Rev Neurosci. 2022 Mar;23(3):173-186. doi: 10.1038/s41583-021-00548-3. Epub 2022 Jan 13.
6
Activity-dependent remodeling of genome architecture in engram cells facilitates memory formation and recall.记忆印迹细胞中依赖于活动的基因组结构重塑促进记忆形成和回忆。
Neural Regen Res. 2022 May;17(5):991-993. doi: 10.4103/1673-5374.324834.
7
The essence of the engram: Cellular or synaptic?记忆痕迹的本质:细胞的还是突触的?
Semin Cell Dev Biol. 2022 May;125:122-135. doi: 10.1016/j.semcdb.2021.05.033. Epub 2021 Jun 5.
8
Transcriptome and epigenome analysis of engram cells: Next-generation sequencing technologies in memory research.记忆研究中的印记细胞的转录组和表观基因组分析:新一代测序技术。
Neurosci Biobehav Rev. 2021 Aug;127:865-875. doi: 10.1016/j.neubiorev.2021.06.010. Epub 2021 Jun 5.
9
Bidirectional perisomatic inhibitory plasticity of a Fos neuronal network.双向 Fos 神经元网络的胞体抑制性可塑性。
Nature. 2021 Feb;590(7844):115-121. doi: 10.1038/s41586-020-3031-0. Epub 2020 Dec 9.
10
Elucidating memory in the brain via single-cell transcriptomics.通过单细胞转录组学揭示大脑中的记忆。
J Neurochem. 2021 May;157(4):982-992. doi: 10.1111/jnc.15250. Epub 2020 Dec 10.