神经退行性变
第一季
线粒体分裂
创伤性脑损伤
医学
慢性创伤性脑病
神经科学
线粒体
线粒体融合
生物
内科学
毒物控制
细胞生物学
精神科
脑震荡
疾病
线粒体DNA
医疗急救
伤害预防
生物化学
基因
作者
Preethy Sridharan,Yeojung Koh,Emiko Miller,Di Hu,Suwarna Chakraborty,Sunil Jamuna Tripathi,Teresa R. Kee,Kalyani Chaubey,Edwin Vázquez‐Rosa,Sarah Barker,Hui Liu,Rose A León-Alvarado,Kathryn Franke,Coral J. Cintrón-Pérez,Matasha Dhar,Min-Kyoo Shin,Margaret E. Flanagan,Rudolph J. Castellani,Tamar Gefen,Marina Bykova
标识
DOI:10.1016/j.xcrm.2024.101715
摘要
Progression of acute traumatic brain injury (TBI) into chronic neurodegeneration is a major health problem with no protective treatments. Here, we report that acutely elevated mitochondrial fission after TBI in mice triggers chronic neurodegeneration persisting 17 months later, equivalent to many human decades. We show that increased mitochondrial fission after mouse TBI is related to increased brain levels of mitochondrial fission 1 protein (Fis1) and that brain Fis1 is also elevated in human TBI. Pharmacologically preventing Fis1 from binding its mitochondrial partner, dynamin-related protein 1 (Drp1), for 2 weeks after TBI normalizes the balance of mitochondrial fission/fusion and prevents chronically impaired mitochondrial bioenergetics, oxidative damage, microglial activation and lipid droplet formation, blood-brain barrier deterioration, neurodegeneration, and cognitive impairment. Delaying treatment until 8 months after TBI offers no protection. Thus, time-sensitive inhibition of acutely elevated mitochondrial fission may represent a strategy to protect human TBI patients from chronic neurodegeneration.
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