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齿状回记忆神经元的θ相特异性调制。

Theta-phase-specific modulation of dentate gyrus memory neurons.

机构信息

Department of Biomedical Engineering, Boston University, Boston, United States.

Center for Systems Neuroscience, Neurophotonics Center, Boston University, Boston, United States.

出版信息

Elife. 2023 Jul 4;12:e82697. doi: 10.7554/eLife.82697.

DOI:10.7554/eLife.82697
PMID:37401757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10361715/
Abstract

The theta rhythm, a quasi-periodic 4-10 Hz oscillation, is observed during memory processing in the hippocampus, with different phases of theta hypothesized to separate independent streams of information related to the encoding and recall of memories. At the cellular level, the discovery of hippocampal memory cells (engram neurons), as well as the modulation of memory recall through optogenetic activation of these cells, has provided evidence that certain memories are stored, in part, in a sparse ensemble of neurons in the hippocampus. In previous research, however, engram reactivation has been carried out using open-loop stimulation at fixed frequencies; the relationship between engram neuron reactivation and ongoing network oscillations has not been taken into consideration. To address this concern, we implemented a closed-loop reactivation of engram neurons that enabled phase-specific stimulation relative to theta oscillations in the local field potential in CA1. Using this real-time approach, we tested the impact of activating dentate gyrus engram neurons during the peak (encoding phase) and trough (recall phase) of theta oscillations. Consistent with previously hypothesized functions of theta oscillations in memory function, we show that stimulating dentate gyrus engram neurons at the trough of theta is more effective in eliciting behavioral recall than either fixed-frequency stimulation or stimulation at the peak of theta. Moreover, phase-specific trough stimulation is accompanied by an increase in the coupling between gamma and theta oscillations in CA1 hippocampus. Our results provide a causal link between phase-specific activation of engram cells and the behavioral expression of memory.

摘要

θ 节律是一种准周期性的 4-10Hz 振荡,在海马体的记忆处理过程中观察到,不同相位的 θ 节律被假设可以分离与记忆编码和回忆相关的独立信息流。在细胞水平上,海马体记忆细胞(记忆神经元)的发现,以及通过这些细胞的光遗传学激活来调节记忆回忆,为某些记忆部分存储在海马体中稀疏的神经元集合中提供了证据。然而,在之前的研究中,使用固定频率的开环刺激来进行记忆再激活;记忆神经元再激活与正在进行的网络振荡之间的关系尚未被考虑在内。为了解决这个问题,我们实现了记忆神经元的闭环再激活,使其能够相对于 CA1 局部场电势中的θ 振荡进行相位特异性刺激。使用这种实时方法,我们测试了在θ 振荡的峰值(编码阶段)和低谷(回忆阶段)期间激活齿状回记忆神经元对行为回忆的影响。与θ 振荡在记忆功能中的先前假设功能一致,我们发现,在θ 振荡的低谷刺激齿状回记忆神经元比固定频率刺激或在θ 振荡的峰值刺激更有效地引发行为回忆。此外,相位特异性低谷刺激伴随着 CA1 海马体中γ 和θ 振荡之间耦合的增加。我们的结果提供了记忆细胞的相位特异性激活与行为表达之间的因果联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/dc2ad566903a/elife-82697-fig5-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/ad0499b4536e/elife-82697-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/04b57e7c024c/elife-82697-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/bed89c5b658f/elife-82697-fig1-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/ea220a3630d6/elife-82697-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/66d1343d2fde/elife-82697-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/5ac4f843a73d/elife-82697-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/710e4c7d0cc3/elife-82697-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/4ff272d08cc1/elife-82697-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/dc2ad566903a/elife-82697-fig5-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/ad0499b4536e/elife-82697-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/04b57e7c024c/elife-82697-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/bed89c5b658f/elife-82697-fig1-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/ea220a3630d6/elife-82697-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/66d1343d2fde/elife-82697-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/5ac4f843a73d/elife-82697-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/710e4c7d0cc3/elife-82697-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/4ff272d08cc1/elife-82697-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ed/10361715/dc2ad566903a/elife-82697-fig5-figsupp2.jpg

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