Hippocampal neuroligin-2 links early-life stress with impaired social recognition and increased aggression in adult mice

神经肽 神经科学 心理学 海马体 海马结构 自闭症 精神分裂症(面向对象编程) 精神科 抑制性突触后电位 兴奋性突触后电位
作者
Christopher Kohl,Xiao‐Dong Wang,Jocelyn Grosse,Céline Fournier,Daniela Harbich,Sören Westerholz,Jitao Li,Alexandre Bacq,Claudia Sippel,Felix Hausch,Carmen Sandi,Mathias V. Schmidt
出处
期刊:Psychoneuroendocrinology [Elsevier BV]
卷期号:55: 128-143 被引量:64
标识
DOI:10.1016/j.psyneuen.2015.02.016
摘要

Early-life stress is a key risk factor for the development of neuropsychiatric disorders later in life. Neuronal cell adhesion molecules have been strongly implicated in the pathophysiology of psychiatric disorders and in modulating social behaviors associated with these diseases. Neuroligin-2 is a synaptic cell adhesion molecule, located at the postsynaptic membrane of inhibitory GABAergic synapses, and is involved in synaptic stabilization and maturation. Alterations in neuroligin-2 expression have previously been associated with changes in social behavior linked to psychiatric disorders, including schizophrenia and autism. In this study, we show that early-life stress, induced by limited nesting and bedding material, leads to impaired social recognition and increased aggression in adult mice, accompanied by increased expression levels of hippocampal neuroligin-2. Viral overexpression of hippocampal neuroligin-2 in adulthood mimics early-life stress-induced alterations in social behavior and social cognition. Moreover, viral knockdown of neuroligin-2 in the adult hippocampus attenuates the early-life stress-induced behavioral changes. Our results highlight the importance of neuroligin-2 in mediating early-life stress effects on social behavior and social cognition and its promising role as a novel therapeutic target for neuropsychiatric disorders.
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