下调和上调
环境富集
社会压力
成纤维细胞生长因子
体育锻炼
慢性应激
心情
应对(心理学)
社会失败
免疫系统
炎症
医学
身体压力
内分泌学
萧条(经济学)
心理学
内科学
肿瘤坏死因子α
社会支持
神经科学
氧化应激
体力活动
促炎细胞因子
血脑屏障
神经可塑性
热应力
心理压力
生长因子
免疫失调
免疫学
生物
战斗或逃跑反应
重性抑郁障碍
作者
Sam E. J. Paton,José L. Solano,Alice Cadoret,Adeline Collignon,Luisa Bandeira Binder,Béatrice Daigle,Laura Menegatti Bevilacqua,Émanuelle Richer,François Coulombe-Rozon,Laurence Dion-Albert,Katarzyna Dudek,Philippe Beauchamp-Kerr,Felix-Antoine Berube,Janick Boissonneault,François Borgeat,Lionel Cailhol,Pierre David,Simon Ducharme,Alexandre Dumais,Helen Findlay
标识
DOI:10.1038/s41467-025-68058-9
摘要
Chronic stress promotes blood-brain barrier (BBB) integrity loss leading to passage of inflammatory mediators in mood-regulating brain areas and establishment of depressive behaviors. Conversely, neurovascular adaptations favoring stress resilience and preventive strategies to promote them are undetermined. We report that environmental enrichment dampens stress-induced loss of endothelial tight junction Claudin-5 (Cldn5) along with anxiety- and depression-like behaviors in male mice via an increase in fibroblast growth factor 2 (Fgf2). Coping with voluntary physical exercise also protects the BBB from stress deleterious effects by increasing Fgf2. Fgf2 is mostly expressed by glial cells, and viral-mediated astrocyte-specific Fgf2 upregulation prevents stress-induced social avoidance while downregulation increases stress susceptibility and blunts physical exercise benefits. Treatment of mouse and human endothelial cells with Fgf2 prior an immune challenge reduces BBB dysfunction, Cldn5 loss, and altered signaling supporting its protective role. Circulating FGF2 level is linked with depression severity and symptomatology in men and women reinforcing involvement of this growth factor in mood disorders.
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