Ziółkowska Magdalena, Sotoudeh Narges, Cały Anna, Puchalska Monika, Pagano Roberto, Śliwińska Malgorzata Alicja, Salamian Ahmad, Radwanska Kasia
Laboratory of Molecular Basis of Behavior, Nencki Institute of Experimental Biology of Polish Academy of Sciences, Warsaw, Poland.
Elife. 2025 Jan 23;13:RP101736. doi: 10.7554/eLife.101736.
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.
在不断变化的环境中消除情境性恐惧的能力对动物生存至关重要。近期数据支持丘脑 reunens 核(RE)及其向背侧海马 CA1 区的投射(RE→dCA1)在此过程中的作用。然而,在情境性恐惧消退(CFE)期间 RE 如何影响 dCA1 神经元仍知之甚少。在这里,我们揭示 RE→dCA1 通路通过影响 CFE 诱导的兴奋性突触分子重塑来促进情境性恐惧的消退。对小鼠的解剖追踪和化学遗传学操作表明,RE 神经元在 dCA1 区的原层(SO)和分子层(SLM)形成突触并调节突触传递,但不在辐射层(SR)。我们还观察到在由 RE 支配的两个层中兴奋性突触的 CFE 特异性结构变化以及突触支架蛋白 PSD - 95 的表达,但在 SR 中未观察到。有趣的是,只有 SLM 中的变化对由 RE 支配的树突是特异性的。为了进一步支持 RE→dCA1 投射在 CFE 中的作用,我们证明在 CFE 过程中对 RE→dCA1 通路进行短暂的化学遗传学抑制会持续损害 CFE 记忆的形成以及 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 突触分子重塑参与 CFE。