小鼠背侧齿状回恐惧刻画细胞的主导活动是恐惧泛化的基础。

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
PLoS Biology Pub Date : 2024-07-12 eCollection Date: 2024-07-01 DOI:10.1371/journal.pbio.3002679
Kun Cui, Xuetao Qi, Zilong Liu, Weiqi Sun, Peijie Jiao, Chang Liu, Jifu Tong, Xiaoyan Sun, Haojie Sun, Su Fu, Jiaxin Wang, Yawen Zheng, Tianyu Liu, Shuang Cui, Fengyu Liu, Jian Mao, Jie Zheng, You Wan, Ming Yi
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引用次数: 0

摘要

过度泛化恐惧是创伤后应激障碍(PTSD)和其他焦虑症特有的一种对无害刺激或情况的适应不良反应。背侧齿状回(dDG)中含有在准确记忆检索中起关键作用的 "刻画 "细胞。然而,人们对 dDG 网络中的神经元亚群在恐惧泛化过程中的协调机制还不甚了解。在这里,我们利用 Tet-off 系统结合免疫染色和双光子钙成像技术,报告了在条件情境中标记的 dDG 恐惧刻画细胞在小鼠表现出泛化恐惧的类似情境中构成了显著较高比例的 dDG 神经元激活。这些编码条件情境的 dDG 恐惧刻画细胞的激活对于诱导小鼠在类似情境中的恐惧泛化既充分又必要。小鼠在类似情境中表现出恐惧泛化时,腹侧齿状回(vMCs)中苔藓细胞的活动会受到显著抑制,激活 vMCs-dDG 通路可以抑制泛化恐惧,但不能抑制条件恐惧。最后,用 "安全 "信号修改 dDG 中的恐惧记忆刻痕可以有效地挽救恐惧泛化。这些发现揭示了 dDG 刻画细胞的竞争优势是恐惧泛化的基础,可以通过激活 vMCs-dDG 通路或修改恐惧记忆刻画来挽救恐惧泛化,并为 dDG 网络作为恐惧泛化的神经元基础提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dominant activities of fear engram cells in the dorsal dentate gyrus underlie fear generalization in mice.

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.

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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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