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伏隔核神经黏附素-2 在抑郁和应激易感性中的细胞类型特异性作用。

Cell-type-specific role for nucleus accumbens neuroligin-2 in depression and stress susceptibility.

机构信息

Fishberg Department of Neuroscience, Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.

Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.

出版信息

Proc Natl Acad Sci U S A. 2018 Jan 30;115(5):1111-1116. doi: 10.1073/pnas.1719014115. Epub 2018 Jan 16.

Abstract

Behavioral coping strategies are critical for active resilience to stress and depression; here we describe a role for neuroligin-2 (NLGN-2) in the nucleus accumbens (NAc). Neuroligins (NLGN) are a family of neuronal postsynaptic cell adhesion proteins that are constituents of the excitatory and inhibitory synapse. Importantly, NLGN-3 and NLGN-4 mutations are strongly implicated as candidates underlying the development of neuropsychiatric disorders with social disturbances such as autism, but the role of NLGN-2 in neuropsychiatric disease states is unclear. Here we show a reduction in NLGN-2 gene expression in the NAc of patients with major depressive disorder. Chronic social defeat stress in mice also decreases NLGN-2 selectively in dopamine D1-positive cells, but not dopamine D2-positive cells, within the NAc of stress-susceptible mice. Functional NLGN-2 knockdown produces bidirectional, cell-type-specific effects: knockdown in dopamine D1-positive cells promotes subordination and stress susceptibility, whereas knockdown in dopamine D2-positive cells mediates active defensive behavior. These findings establish a behavioral role for NAc NLGN-2 in stress and depression; provide a basis for targeted, cell-type specific therapy; and highlight the role of active behavioral coping mechanisms in stress susceptibility.

摘要

行为应对策略对于积极应对压力和抑郁至关重要;在这里,我们描述了神经黏附素-2 (NLGN-2) 在伏隔核 (NAc) 中的作用。神经黏附素 (NLGN) 是一组神经元突触后细胞黏附蛋白,是兴奋性和抑制性突触的组成部分。重要的是,NLGN-3 和 NLGN-4 突变被强烈认为是导致神经精神疾病发展的候选物,这些疾病伴有社交障碍,如自闭症,但 NLGN-2 在神经精神疾病状态中的作用尚不清楚。在这里,我们发现在患有重度抑郁症的患者的 NAc 中 NLGN-2 基因表达减少。慢性社交挫败应激也会选择性地减少应激易感小鼠 NAc 中多巴胺 D1 阳性细胞内的 NLGN-2,但不会减少多巴胺 D2 阳性细胞内的 NLGN-2。功能性 NLGN-2 敲低产生双向、细胞类型特异性的效应:在多巴胺 D1 阳性细胞内敲低会促进从属和应激易感性,而在多巴胺 D2 阳性细胞内敲低则介导主动防御行为。这些发现确立了 NAc NLGN-2 在应激和抑郁中的行为作用;为靶向、细胞类型特异性治疗提供了基础;并强调了积极行为应对机制在应激易感性中的作用。

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