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恐惧记忆细胞在小鼠背齿状回中的主导活动是恐惧泛化的基础。

Dominant activities of fear engram cells in the dorsal dentate gyrus underlie fear generalization in mice.

机构信息

Neuroscience Research Institute and Department of Neurobiology, School of Basic Medical Sciences, Peking University, Beijing, China.

Beijing Life Science Academy, Beijing, China.

出版信息

PLoS Biol. 2024 Jul 12;22(7):e3002679. doi: 10.1371/journal.pbio.3002679. eCollection 2024 Jul.

Abstract

Over-generalized fear is a maladaptive response to harmless stimuli or situations characteristic of posttraumatic stress disorder (PTSD) and other anxiety disorders. The dorsal dentate gyrus (dDG) contains engram cells that play a crucial role in accurate memory retrieval. However, the coordination mechanism of neuronal subpopulations within the dDG network during fear generalization is not well understood. Here, with the Tet-off system combined with immunostaining and two-photon calcium imaging, we report that dDG fear engram cells labeled in the conditioned context constitutes a significantly higher proportion of dDG neurons activated in a similar context where mice show generalized fear. The activation of these dDG fear engram cells encoding the conditioned context is both sufficient and necessary for inducing fear generalization in the similar context. Activities of mossy cells in the ventral dentate gyrus (vMCs) are significantly suppressed in mice showing fear generalization in a similar context, and activating the vMCs-dDG pathway suppresses generalized but not conditioned fear. Finally, modifying fear memory engrams in the dDG with "safety" signals effectively rescues fear generalization. These findings reveal that the competitive advantage of dDG engram cells underlies fear generalization, which can be rescued by activating the vMCs-dDG pathway or modifying fear memory engrams, and provide novel insights into the dDG network as the neuronal basis of fear generalization.

摘要

过度泛化的恐惧是对无害刺激或情境的一种适应不良反应,是创伤后应激障碍(PTSD)和其他焦虑障碍的特征。背齿状回(dDG)包含记忆细胞,它们在准确记忆检索中起着至关重要的作用。然而,dDG 网络内神经元亚群在恐惧泛化过程中的协调机制尚不清楚。在这里,我们使用 Tet-off 系统结合免疫染色和双光子钙成像,报告说在条件化环境中标记的 dDG 恐惧记忆细胞构成了在类似环境中激活的 dDG 神经元的显著更高比例,而在类似环境中,小鼠表现出恐惧泛化。这些编码条件化环境的 dDG 恐惧记忆细胞的激活对于在类似环境中诱导恐惧泛化既充分又必要。在类似环境中表现出恐惧泛化的小鼠中,腹侧齿状回(vMCs)中的苔藓细胞的活动显著受到抑制,而激活 vMCs-dDG 通路抑制了泛化但不抑制条件性恐惧。最后,用“安全”信号修改 dDG 中的恐惧记忆印迹可以有效地挽救恐惧泛化。这些发现揭示了 dDG 记忆细胞的竞争优势是恐惧泛化的基础,通过激活 vMCs-dDG 通路或修改恐惧记忆印迹可以挽救恐惧泛化,为 dDG 网络作为恐惧泛化的神经元基础提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8f2/11244812/3b71613bb0bb/pbio.3002679.g001.jpg

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