星形胶质增生
中性粒细胞胞外陷阱
刺激
细胞外
神经科学
脂质运载蛋白
条件基因敲除
冲程(发动机)
心理学
小胶质细胞
基因剔除小鼠
串扰
免疫系统
星形胶质细胞
薄壁组织
机制(生物学)
共刺激
医学
血脑屏障
磁刺激
脑刺激
神经炎症
细胞内
信号转导
胶质增生
免疫失调
人脑
免疫学
刺激(心理学)
脑损伤
生物
炎症
细胞生物学
中枢神经系统
作者
Yuan Liu,Wei Lin,Zhongfei Bai,Yu‐Wei Ge,Yuanjie Xiao,Feifei Zhu,Jing Zhang,Bingying Wang,Qiyang Li,Li Gao,Yan Li,Chunlei Shan,Jun Nagai,Yiwen Wu,Tian‐Le Xu,Zhengrun Gao
出处
期刊:Neuron
[Cell Press]
日期:2025-10-10
卷期号:113 (24): 4199-4216.e8
被引量:6
标识
DOI:10.1016/j.neuron.2025.09.018
摘要
Patients with an ischemic stroke are often predisposed to emotional disorders. However, the mechanisms underlying post-stroke emotional disorders (PSEDs) remain unclear. Recent research highlights the role of neuroinflammation, driven primarily by infiltration of circulating immune cells within the brain parenchyma and accompanied by blood-brain barrier (BBB) disruption, in secondary emotional disorders. Combining human cohort and animal model data, we identified serum neutrophil extracellular traps (NETs) as significant contributors to PSEDs. Conditional knockout strategies and -omics analyses convergently identified central NETs as the specific modulator of PSEDs. We further elucidated that astrogliosis is catalyzed by lipocalin 2 (Lcn2) released from NETs, which constituted the core mechanism underlying PSEDs. Additionally, we provided proof-of-concept evidence that transcranial direct current stimulation (tDCS) can suppress Lcn2 release and alleviate PSEDs. Collectively, these findings delineated a distinct peripheral-central neuroimmune interaction pattern following BBB damage and highlighted the potential of non-invasive stimulation in effectively reshaping the neuroimmune environment.
科研通智能强力驱动
Strongly Powered by AbleSci AI