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GluRδ2 Expression in the Mature Cerebellum of Hotfoot Mice Promotes Parallel Fiber Synaptogenesis and Axonal Competition

机译:热足小鼠成熟小脑中的GluRδ2表达促进平行纤维突触发生和轴突竞争。

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摘要

Glutamate receptor delta 2 (GluRδ2) is selectively expressed in the cerebellum, exclusively in the spines of the Purkinje cells (PCs) that are in contact with parallel fibers (PFs). Although its structure is similar to ionotropic glutamate receptors, it has no channel function and its ligand is unknown. The GluRδ2-null mice, such as knockout and hotfoot have profoundly altered cerebellar circuitry, which causes ataxia and impaired motor learning. Notably, GluRδ2 in PC-PF synapses regulates their maturation and strengthening and induces long term depression (LTD). In addition, GluRδ2 participates in the highly territorial competition between the two excitatory inputs to the PC; the climbing fiber (CF), which innervates the proximal dendritic compartment, and the PF, which is connected to spiny distal branchlets. Recently, studies have suggested that GluRδ2 acts as an adhesion molecule in PF synaptogenesis. Here, we provide in vivo and in vitro evidence that supports this hypothesis. Through lentiviral rescue in hotfoot mice, we noted a recovery of PC-PF contacts in the distal dendritic domain. In the proximal domain, we observed the formation of new spines that were innervated by PFs and a reduction in contact with the CF; ie, the pattern of innervation in the PC shifted to favor the PF input. Moreover, ectopic expression of GluRδ2 in HEK293 cells that were cocultured with granule cells or in cerebellar Golgi cells in the mature brain induced the formation of new PF contacts. Collectively, our observations show that GluRδ2 is an adhesion molecule that induces the formation of PF contacts independently of its cellular localization and promotes heterosynaptic competition in the PC proximal dendritic domain.
机译:谷氨酸受体δ2(GluRδ2)在小脑中选择性表达,仅在与平行纤维(PF)接触的Purkinje细胞(PC)的棘中表达。尽管其结构与离子型谷氨酸受体相似,但它不具有通道功能,并且其配体未知。 GluRδ2无效的小鼠,如基因敲除和热脚,已彻底改变了小脑回路,从而导致共济失调和运动学习障碍。值得注意的是,PC-PF突触中的GluRδ2调节其成熟和增强,并诱发长期抑郁症(LTD)。此外,GluRδ2参与了PC的两个兴奋性输入之间的高度领土竞争;支配近端树突状区室的攀爬纤维(CF)和与多刺的远端小枝相连的PF。最近,研究表明,GluRδ2在PF突触形成中起黏附分子的作用。在这里,我们提供了支持这一假设的体内和体外证据。通过热脚小鼠的慢病毒抢救,我们注意到远端树突域中PC-PF接触的恢复。在近端区域,我们观察到由PF支配的新棘的形成以及与CF接触的减少。也就是说,PC中的神经支配模式发生了变化,从而有利于PF输入。此外,在成熟的脑中与颗粒细胞或小脑高尔基细胞共培养的HEK293细胞中GluRδ2的异位表达诱导了新的PF接触的形成。总的来说,我们的观察结果表明,GluRδ2是一种粘附分子,可独立于其细胞定位而诱导PF接触的形成,并促进PC近端树突结构域中的异突触竞争。

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