Otsubo Keisuke, Sakashita Naoko, Nishimoto Yuki, Sato Yo, Tsutsui Takehisa, Kobayashi Katsunori, Suzuki Kanzo, Segi-Nishida Eri
Department of Biological Science and Technology, Faculty of Advanced Engineering, Tokyo University of Science, Tokyo, Japan.
Department of Pharmacology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Front Neurosci. 2024 Aug 8;18:1418058. doi: 10.3389/fnins.2024.1418058. eCollection 2024.
Desmoplakin (Dsp) is a component of desmosomal cell-cell junctions that interacts with the cadherin complex and cytoskeletal intermediate filaments. In addition to its function as an adhesion component, Dsp is involved in various biological processes, such as gene expression, differentiation, and migration. Dsp is specifically expressed in the hippocampal dentate gyrus (DG) in the central nervous system. However, it is unclear how Dsp impacts hippocampal function and its related behaviors. Using an adeno-associated virus knockdown system in mice, we provide evidence that Dsp in the DG maintains hippocampal functions, including neuronal activity and adult neurogenesis, and contributes to anxiolytic-like effects. Dsp protein is mostly localized in mature granule cells in the adult DG. Dsp knockdown in the DG resulted in a lowered expression of an activity-dependent transcription factor FosB, and an increased expression of mature neuronal markers, such as calbindin. In addition, the suppression of Dsp decreases serotonin responsiveness at the DG output mossy fiber synapses and alters adult neurogenic processes in the subgranular zone of the DG. Moreover, DG-specific Dsp knockdown mice showed an increase in anxiety-like behaviors. Taken together, this research uncovers an unexplored function for Dsp in the central nervous system and suggests that Dsp in the DG may function as a regulator to maintain proper neuronal activation and adult neurogenesis, and contribute to the adaptation of emotion-related behavior.
桥粒斑蛋白(Dsp)是桥粒细胞间连接的一个组成部分,它与钙黏蛋白复合体和细胞骨架中间丝相互作用。除了作为一种黏附成分发挥作用外,Dsp还参与多种生物学过程,如基因表达、分化和迁移。Dsp在中枢神经系统的海马齿状回(DG)中特异性表达。然而,尚不清楚Dsp如何影响海马功能及其相关行为。利用小鼠腺相关病毒敲低系统,我们提供证据表明,DG中的Dsp维持海马功能,包括神经元活动和成年神经发生,并有助于产生抗焦虑样效应。Dsp蛋白主要定位于成年DG中的成熟颗粒细胞。DG中Dsp的敲低导致活性依赖转录因子FosB的表达降低,以及成熟神经元标志物如钙结合蛋白的表达增加。此外,Dsp的抑制降低了DG输出苔藓纤维突触处的5-羟色胺反应性,并改变了DG颗粒下区的成年神经发生过程。此外,DG特异性Dsp敲低小鼠表现出焦虑样行为增加。综上所述,本研究揭示了Dsp在中枢神经系统中尚未被探索的功能,并表明DG中的Dsp可能作为一种调节因子,维持适当的神经元激活和成年神经发生,并有助于情绪相关行为的适应。