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神经退行性疾病和中枢神经系统损伤中的小胶质细胞程序性细胞死亡。

Microglia programmed cell death in neurodegenerative diseases and CNS injury.

作者信息

Cai Ling, Fan Qiuyue, Pang Rui, Chen Chen, Zhang Yueman, Xie Haiyi, Huang Jingyi, Wang Yu, Li Peiying, Huang Dan, Jin Xia, Zhou Yuxi, Li Yan

机构信息

Department of Anesthesiology, Key Laboratory of the Ministry of Education, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Clinical Research Center, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Apoptosis. 2025 Feb;30(1-2):446-465. doi: 10.1007/s10495-024-02041-5. Epub 2024 Dec 10.

Abstract

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.

摘要

程序性细胞死亡(PCD)已成为各种病理状况发生和发展过程中的关键调节机制。小胶质细胞中的PCD,包括坏死性凋亡、炎性小体介导的细胞焦亡、凋亡、铁死亡和自噬,发生在多种中枢神经系统(CNS)疾病中。小胶质细胞失调可导致中枢神经系统损伤时组织过度损伤或神经元死亡。各种损伤刺激触发小胶质细胞PCD途径的异常激活,进而进一步导致炎症级联反应,在恶性循环中加剧中枢神经系统病理变化。因此,靶向小胶质细胞中的PCD被认为是治疗各种神经退行性疾病和中枢神经系统损伤的重要途径。在本综述中,我们总结了主要的和最近的研究发现,重点关注小胶质细胞中PCD调节神经退行性疾病和中枢神经系统损伤功能的机制,并对目前针对各种PCD途径的抑制剂进行系统概述,这可能提供值得进一步研究的重要治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8047/11799081/fb4892aebf96/10495_2024_2041_Fig1_HTML.jpg

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