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超分辨3D-STED显微镜技术揭示了神经连接蛋白3基因敲除小鼠海马CA1区兴奋性突触的层特异性增加。

Super-resolved 3D-STED microscopy identifies a layer-specific increase in excitatory synapses in the hippocampal CA1 region of Neuroligin-3 KO mice.

作者信息

Koganezawa Noriko, Hanamura Kenji, Schwark Manuela, Krueger-Burg Dilja, Kawabe Hiroshi

机构信息

Department of Pharmacology, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma 371-8511, Japan.

Department of Molecular Neurobiology, Max Planck Institute of Experimental Medicine, Hermann-Rein-Strasse 3, 37075 Göttingen, Germany.

出版信息

Biochem Biophys Res Commun. 2021 Dec 10;582:144-149. doi: 10.1016/j.bbrc.2021.10.003. Epub 2021 Oct 7.

DOI:10.1016/j.bbrc.2021.10.003
PMID:34715405
Abstract

The chemical synapse is one type of cell-adhesion system that transmits information from a neuron to another neuron in the complex neuronal network in the brain. Synaptic transmission is the rate-limiting step during the information processing in the neuronal network and its plasticity is involved in cognitive functions. Thus, morphological and electrophysiological analyses of synapses are of particular importance in neuroscience research. In the current study, we applied super-resolved three-dimensional stimulated emission depletion (3D-STED) microscopy for the morphological analyses of synapses. This approach allowed us to estimate the precise number of excitatory and inhibitory synapses in the mouse hippocampal tissue. We discovered a region-specific increase in excitatory synapses in a model mouse of autism spectrum disorder, Neuroligin-3 KO, with this method. This type of analysis will open a new field in developmental neuroscience in the future.

摘要

化学突触是一种细胞粘附系统,在大脑复杂的神经元网络中,它能将信息从一个神经元传递到另一个神经元。突触传递是神经元网络信息处理过程中的限速步骤,其可塑性与认知功能有关。因此,对突触进行形态学和电生理学分析在神经科学研究中尤为重要。在本研究中,我们应用超分辨三维受激发射损耗(3D-STED)显微镜对突触进行形态学分析。这种方法使我们能够估计小鼠海马组织中兴奋性和抑制性突触的精确数量。通过这种方法,我们在自闭症谱系障碍模型小鼠Neuroligin-3基因敲除小鼠中发现了兴奋性突触的区域特异性增加。这种类型的分析将在未来为发育神经科学开辟一个新领域。

相似文献

1
Super-resolved 3D-STED microscopy identifies a layer-specific increase in excitatory synapses in the hippocampal CA1 region of Neuroligin-3 KO mice.超分辨3D-STED显微镜技术揭示了神经连接蛋白3基因敲除小鼠海马CA1区兴奋性突触的层特异性增加。
Biochem Biophys Res Commun. 2021 Dec 10;582:144-149. doi: 10.1016/j.bbrc.2021.10.003. Epub 2021 Oct 7.
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Conditional ablation of neuroligin-1 in CA1 pyramidal neurons blocks LTP by a cell-autonomous NMDA receptor-independent mechanism.在CA1锥体神经元中条件性敲除神经连接蛋白-1,可通过一种细胞自主的、不依赖N-甲基-D-天冬氨酸受体的机制阻断长时程增强。
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引用本文的文献

1
Insights into the structure and function of the hippocampus: implications for the pathophysiology and treatment of autism spectrum disorder.对海马体结构与功能的洞察:对自闭症谱系障碍病理生理学及治疗的启示
Front Psychiatry. 2024 Apr 23;15:1364858. doi: 10.3389/fpsyt.2024.1364858. eCollection 2024.
2
Region-Specific Phosphorylation Determines Neuroligin-3 Localization to Excitatory Versus Inhibitory Synapses.区域特异性磷酸化决定了神经黏连蛋白 3 定位到兴奋性突触还是抑制性突触。
Biol Psychiatry. 2024 Nov 15;96(10):815-828. doi: 10.1016/j.biopsych.2023.12.020. Epub 2023 Dec 27.
3
Complex spiking neural networks with synaptic time-delay based on anti-interference function.
基于抗干扰功能的具有突触时延的复杂脉冲神经网络。
Cogn Neurodyn. 2022 Dec;16(6):1485-1503. doi: 10.1007/s11571-022-09803-4. Epub 2022 Apr 15.