萧条(经济学)
扁桃形结构
医学
神经科学
内科学
内分泌学
生物
中枢神经系统
心理学
生物信息学
年轻人
疾病
基因
炎症
转录组
信号转导
基因表达
海马体
免疫学
作者
Yue You,Chang-Ting Lv,Peng-Tao Ni,Shi-Jie Wang,Le Liu,Yu-Tong Song,Ze Hui,Yao Huang,Yao Liu,Kun Tong,Jing‐Ru Hao,Nan Sun,Jun-Li Cao,Can Gao
出处
期刊:Cell Reports
[Cell Press]
日期:2026-04-01
卷期号:45 (4): 117281-117281
标识
DOI:10.1016/j.celrep.2026.117281
摘要
Adolescent stress increases susceptibility to adult depression, potentially by encoding negative memories in stress-responsive neuronal ensembles, though the mechanisms remain unclear. In this study, we use a social defeat stress model with Tet-off labeling to examine the effects of short-term stress during adolescence and adulthood on behavior and cellular changes. Adolescent stress generates denser, more excitable stress-responsive neuronal ensembles in the basolateral amygdala (BLA) compared to adult stress, suggesting persistent traces of early-life stress that heighten remote depression risk. Adolescent mice display underdeveloped, hypoactive parvalbumin (PV) interneurons in the BLA, further suppressed by microglial phagocytic activity. Bidirectional modulation of BLA stress-responsive neuronal ensembles or PV neurons significantly alters depression-like behaviors. Overall, our findings indicate that BLA stress-responsive neuronal ensembles mediate differences in depression susceptibility between adolescent and adult stressed mice, with microglial dysfunction impairing PV neuron inhibitory control. These insights offer potential targets for early intervention in adult depression.
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