Projections from thalamic nucleus reuniens to hippocampal CA1 area participate in context fear extinction by affecting extinction-induced molecular remodeling of excitatory synapses.

IF 6.4 1区 生物学 Q1 BIOLOGY eLife Pub Date : 2025-01-23 DOI:10.7554/eLife.101736
Magdalena Ziółkowska, Narges Sotoudeh, Anna Cały, Monika Puchalska, Roberto Pagano, Malgorzata Alicja Śliwińska, Ahmad Salamian, Kasia Radwanska
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Abstract

The ability to extinguish contextual fear in a changing environment is crucial for animal survival. Recent data support the role of the thalamic nucleus reuniens (RE) and its projections to the dorsal hippocampal CA1 area (RE→dCA1) in this process. However, it remains poorly understood how RE impacts dCA1 neurons during contextual fear extinction (CFE). Here, we reveal that the RE→dCA1 pathway contributes to the extinction of contextual fear by affecting CFE-induced molecular remodeling of excitatory synapses. Anatomical tracing and chemogenetic manipulation in mice demonstrate that RE neurons form synapses and regulate synaptic transmission in the stratum oriens (SO) and lacunosum-moleculare (SLM) of the dCA1 area, but not in the stratum radiatum (SR). We also observe CFE-specific structural changes of excitatory synapses and expression of the synaptic scaffold protein, PSD-95, in both strata innervated by RE, but not in SR. Interestingly, only the changes in SLM are specific for the dendrites innervated by RE. To further support the role of the RE→dCA1 projection in CFE, we demonstrate that brief chemogenetic inhibition of the RE→dCA1 pathway during a CFE session persistently impairs the formation of CFE memory and CFE-induced changes of PSD-95 levels in SLM. Thus, our data indicate that RE participates in CFE by regulating CFE-induced molecular remodeling of dCA1 synapses.

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丘脑团聚核向海马CA1区的投射通过影响消失诱导的兴奋性突触分子重塑参与情境恐惧消退。
在不断变化的环境中消除情境恐惧的能力对动物的生存至关重要。最近的数据支持了丘脑团聚核(RE)及其向海马背侧CA1区(RE→dCA1)的投射在这一过程中的作用。然而,人们对RE在情境恐惧消退(CFE)过程中如何影响dCA1神经元仍知之甚少。本研究发现,RE→dCA1通路通过影响cfe诱导的兴奋性突触的分子重塑,有助于情境恐惧的消除。小鼠解剖示迹和化学发生操作表明,RE神经元在dCA1区域的oriens地层(SO)和lacunosum-molecular (SLM)中形成突触并调节突触传递,而在radiatum地层(SR)中不形成突触。我们还观察到,在RE神经支配的两层中,兴奋性突触和突触支架蛋白PSD-95的表达发生了CFE特异性的结构变化,而在sr神经支配的两层中则没有。有趣的是,只有SLM的变化是RE神经支配的树突所特有的。我们证明,在CFE过程中,RE→dCA1通路的短暂化学发生抑制持续地损害了CFE记忆的形成和CFE诱导的SLM中PSD-95水平的变化。因此,我们的数据表明,RE通过调节CFE诱导的dCA1突触的分子重塑参与CFE。
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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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