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大脑皮层杏仁核巩固了一种社会传递的长期记忆。

The cortical amygdala consolidates a socially transmitted long-term memory.

机构信息

Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA, USA.

Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA, USA.

出版信息

Nature. 2024 Aug;632(8024):366-374. doi: 10.1038/s41586-024-07632-5. Epub 2024 Jul 3.

Abstract

Social communication guides decision-making, which is essential for survival. Social transmission of food preference (STFP) is an ecologically relevant memory paradigm in which an animal learns a desirable food odour from another animal in a social context, creating a long-term memory. How food-preference memory is acquired, consolidated and stored is unclear. Here we show that the posteromedial nucleus of the cortical amygdala (COApm) serves as a computational centre in long-term STFP memory consolidation by integrating social and sensory olfactory inputs. Blocking synaptic signalling by the COApm-based circuit selectively abolished STFP memory consolidation without impairing memory acquisition, storage or recall. COApm-mediated STFP memory consolidation depends on synaptic inputs from the accessory olfactory bulb and on synaptic outputs to the anterior olfactory nucleus. STFP memory consolidation requires protein synthesis, suggesting a gene-expression mechanism. Deep single-cell and spatially resolved transcriptomics revealed robust but distinct gene-expression signatures induced by STFP memory formation in the COApm that are consistent with synapse restructuring. Our data thus define a neural circuit for the consolidation of a socially communicated long-term memory, thereby mechanistically distinguishing protein-synthesis-dependent memory consolidation from memory acquisition, storage or retrieval.

摘要

社会交流指导决策,这对生存至关重要。社会传递食物偏好(STFP)是一种生态相关的记忆范式,在这种范式中,动物在社会环境中从另一种动物那里学习到一种令人向往的食物气味,从而产生长期记忆。食物偏好记忆是如何获得、巩固和存储的尚不清楚。在这里,我们表明,皮质杏仁核的后内侧核(COApm)作为一个计算中心,通过整合社会和感官嗅觉输入,在长期 STFP 记忆巩固中发挥作用。基于 COApm 的电路的突触信号阻断选择性地消除了 STFP 记忆巩固,而不会损害记忆的获得、存储或回忆。COApm 介导的 STFP 记忆巩固依赖于副嗅球的突触输入和前嗅核的突触输出。STFP 记忆巩固需要蛋白质合成,表明存在基因表达机制。单细胞深度和空间分辨转录组学揭示了 COApm 中由 STFP 记忆形成诱导的强大但独特的基因表达特征,与突触重构一致。因此,我们的数据定义了一个用于巩固社交交流的长期记忆的神经回路,从而从机制上区分了依赖于蛋白质合成的记忆巩固与记忆的获得、存储或检索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08fc/11306109/7d4f680e4b90/41586_2024_7632_Fig1_HTML.jpg

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