Dorsal CA1 NECTIN3 Reduction Mediates Early-Life Stress-Induced Object Recognition Memory Deficits in Adolescent Female Mice  

作　　者：Yu-Nu Ma Chen-Chen Zhang Ya-Xin Sun Xiao Liu Xue-Xin Li Han Wang Ting Wang Xiao-Dong Wang Yun-Ai Su Ji-Tao Li Tian-Mei Si 

机构地区：[1]Peking University Sixth Hospital,Peking University Institute of Mental Health,NHC Key Laboratory of Mental Health(Peking University),National Clinical Research Center for Mental Disorders(Peking University Sixth Hospital),Beijing,100191,China [2]Department of Neurobiology,Key Laboratory of Medical Neurobiology of Ministry of Health of China,Zhejiang Province Key Laboratory of Neurobiology,Zhejiang University School of Medicine,Hangzhou,310058,China

出　　处：《Neuroscience Bulletin》2025年第2期243-260,共18页神经科学通报(英文版)

基　　金：supported by the National Natural Science Foundation of China(82271569,82001418,82371530,82171529,and 82071528);the Beijing Natural Science Foundation(7222236);the Capital Medical Development Research Fund(2022-1-4111)。

摘　　要：Early-life stress(ES)leads to cognitive dysfunction in female adolescents,but the underlying neural mechanisms remain elusive.Recent evidence suggests that the cell adhesion molecules NECTIN1 and NECTIN3 play a role in cognition and ES-related cognitive deficits in male rodents.In this study,we aimed to investigate whether and how nectins contribute to ES-induced cognitive dysfunction in female adolescents.Applying the well-established limited bedding and nesting material paradigm,we found that ES impairs recognition memory,suppresses prefrontal NECTIN1 and hippocampal NECTIN3 expression,and upregulates corticotropin-releasing hormone(Crh)and its receptor 1(Crhr1)mRNA levels in the hippocampus of adolescent female mice.Genetic experiments revealed that the reduction of dorsal CA1(dCA1)NECTIN3 mediates ES-induced object recognition memory deficits,as knocking down dCA1 NECTIN3 impaired animals’performance in the novel object recognition task,while overexpression of dCA1 NECTIN3 successfully reversed the ES-induced deficits.Notably,prefrontal NECTIN1 knockdown did not result in significant cognitive impairments.Furthermore,acute systemic administration of antalarmin,a CRHR1 antagonist,upregulated hippocampal NECTIN3 levels and rescued object and spatial memory deficits in stressed mice.Our findings underscore the critical role of dCA1 NECTIN3 in mediating ES-induced object recognition memory deficits in adolescent female mice,highlighting it as a potential therapeutic target for stress-related psychiatric disorders in women.

关 键 词：Early-life stress COGNITION NECTIN3 HIPPOCAMPUS FEMALE 

分 类 号：R749.92[医药卫生—神经病学与精神病学]