坏死性下垂
上睑下垂
小胶质细胞
程序性细胞死亡
自噬
神经科学
神经炎症
中枢神经系统
神经退行性变
生物
细胞凋亡
医学
炎症
免疫学
病理
疾病
生物化学
作者
Ling Cai,Qiuyue Fan,Rui Pang,Chen Chen,Yueman Zhang,Haiyi Xie,Jingyi Huang,Yu Wang,Peiying Li,Dan Huang,Xia Jin,Yuxi Zhou,Yan Li
出处
期刊:Apoptosis
[Springer Nature]
日期:2024-12-10
标识
DOI:10.1007/s10495-024-02041-5
摘要
Programmed cell death (PCD) has emerged as a critical regulatory mechanism in the initiation and progression of various pathological conditions. PCD in microglia, including necroptosis, pyroptosis, apoptosis, ferroptosis, and autophagy, occurs in a variety of central nervous system (CNS) diseases. Dysregulation of microglia can lead to excessive tissue damage or neuronal death in CNS injury. Various injury stimuli trigger aberrant activation of the PCD pathway of microglia, which then further leads to inflammatory cascades that exacerbates CNS pathology in a vicious cycle. Therefore, targeting PCD in microglia is considered an important avenue for the treatment of various neurodegenerative diseases and CNS injury. In this review, we summarize the major and recent findings focusing on the mechanisms of PCD in microglia modulating functions in neurodegenerative diseases and CNS injury and provide a systematic overview of the current inhibitors targeting various PCD pathways, which may provide important therapeutic targets that merit further investigation.
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