Institute of Clinical Neuroanatomy, Dr. Senckenberg Anatomy, Neuroscience Center, D-60590 Frankfurt/Main, Germany.
Cereb Cortex. 2020 Apr 14;30(4):2185-2198. doi: 10.1093/cercor/bhz231.
The plasticity-related protein Synaptopodin (SP) has been implicated in neuronal plasticity. SP is targeted to dendritic spines and the axon initial segment, where it organizes the endoplasmic reticulum (ER) into the spine apparatus and the cisternal organelle, respectively. Here, we report an inducible third localization of SP in the somata of activated granule cell ensembles in mouse dentate gyrus. Using immunofluorescence and fluorescence in situ hybridization, we observed a subpopulation of mature granule cells (1-2%) exhibiting perinuclear SP protein and a strong somatic SP mRNA signal. Double immunofluorescence labeling for Arc demonstrated that ~ 75% of these somatic SP-positive cells are also Arc-positive. Placement of mice into a novel environment caused a rapid (2-4 h) induction of Arc, SP mRNA, and SP protein in exploration-induced granule cell ensembles. Lesion experiments showed that this induction requires input from the entorhinal cortex. Somatic SP colocalized with α-Actinin2, a known binding partner of SP. Finally, ultrastructural analysis revealed SP immunoprecipitate on dense plates linking cytoplasmic and perinuclear ER cisterns; these structures were absent in granule cells of SP-deficient mice. Our data implicate SP in the formation of contextual representations in the dentate gyrus and the behaviorally induced reorganization of cytoplasmic and perinuclear ER.
突触相关蛋白(Synaptopodin,SP)是一种与可塑性相关的蛋白,它与神经元可塑性有关。SP 靶向树突棘和轴突起始段,在这些部位,它分别将内质网(endoplasmic reticulum,ER)组织成棘器和 cisternal 细胞器。在这里,我们报告了 SP 在激活的颗粒细胞聚集体的胞体中的第三诱导定位。通过免疫荧光和荧光原位杂交,我们观察到成熟颗粒细胞的亚群(约 1-2%)表现出核周 SP 蛋白和强烈的体 SP mRNA 信号。Arc 的双重免疫荧光标记表明,这些体 SP 阳性细胞中约 75%也是 Arc 阳性的。将小鼠置于新环境中会导致探索诱导的颗粒细胞聚集体中快速(~2-4 h)诱导 Arc、SP mRNA 和 SP 蛋白。损伤实验表明,这种诱导需要来自内嗅皮层的输入。体 SP 与 α-Actinin2 共定位,后者是 SP 的已知结合伴侣。最后,超微结构分析显示 SP 免疫沉淀在连接细胞质和核周 ER 腔的致密板上;在 SP 缺陷型小鼠的颗粒细胞中不存在这些结构。我们的数据表明 SP 参与了齿状回中上下文表示的形成以及细胞质和核周 ER 的行为诱导重组。