PV-dependent reorganization of prelimbic cortex sub-engrams during systems consolidation.

IF 15 1区 医学 Q1 NEUROSCIENCES
Ali Golbabaei, Sheena A Josselyn, Paul W Frankland
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引用次数: 0

Abstract

Active ensembles of neurons form an engram during learning. However, engrams are not immutable, and their organization may change with time via systems consolidation. Here, we labeled engram ensembles in the prelimbic (PrL) cortex during contextual fear conditioning. We found that distinct engram subpopulations ("sub-engrams") contribute to memory recall at recent versus remote delays, with sub-engram contribution determined by their projection profile. At recent delays, sub-engrams projecting to the basal amygdala (BA) and lateral entorhinal cortex (LEC) are activated, and their activity is necessary and sufficient for memory retrieval. At remote delays, sub-engrams projecting to the nucleus reuniens (NRe) and nucleus accumbens (NAc) are additionally recruited, and their activity is necessary and sufficient for memory retrieval. Recruitment of NRe- and NAc-projecting sub-engrams to remote recall is an active process, depending on post-training activation of PrL parvalbumin-expressing interneurons. Post-training chemogenetic inhibition of PrL parvalbumin-expressing interneurons prevented sub-engram recruitment and impaired remote memory.

系统巩固过程中前额叶皮层亚印痕的pv依赖性重组。
在学习过程中,活跃的神经元集合形成了一个印痕。然而,印痕不是不可改变的,它们的组织可能会随着时间的推移而通过系统整合而改变。在这里,我们标记了情景恐惧条件反射过程中前脑边缘(PrL)皮层的印痕集合。我们发现不同的印痕亚群(“子印痕”)对最近和远程延迟的记忆回忆有贡献,而子印痕的贡献取决于它们的投影轮廓。在最近的延迟中,投射到基底杏仁核(BA)和外侧内嗅皮层(LEC)的亚印痕被激活,它们的活动对于记忆恢复是必要和充分的。在远距离延迟时,投射到团聚核(NRe)和伏隔核(NAc)的亚印痕被额外招募,它们的活动对于记忆提取是必要和充分的。在远程回忆中,NRe-和nac -投射子印子的招募是一个活跃的过程,这取决于训练后表达PrL小蛋白的中间神经元的激活。训练后,表达PrL小蛋白的中间神经元的化学发生抑制阻止亚印痕招募和远程记忆受损。
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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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