线粒体 DAMPs:神经炎症和神经退行性疾病发病机制的关键媒介。

IF 4.6 2区 医学 Q1 NEUROSCIENCES Neuropharmacology Pub Date : 2024-11-16 DOI:10.1016/j.neuropharm.2024.110217
Haihan Yu, Kaidi Ren, Yage Jin, Li Zhang, Hui Liu, Zhen Huang, Ziheng Zhang, Xing Chen, Yang Yang, Ziqing Wei
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引用次数: 0

摘要

阿尔茨海默病(AD)、帕金森病(PD)、亨廷顿病(HD)和肌萎缩侧索硬化症(ALS)等神经退行性疾病越来越多地与线粒体功能障碍和神经炎症有关。这种联系的核心是线粒体损伤相关分子模式(mtDAMPs),包括线粒体 DNA、ATP 和活性氧,它们在线粒体应激或损伤过程中释放出来。这些 mtDAMPs 会激活炎症通路,如 NLRP3 炎症小体和 cGAS-STING,从而导致神经退行性疾病的恶化。本综述深入探讨了 mtDAMPs 驱动神经炎症的机制,并讨论了针对这些通路的潜在治疗策略,以缓解神经退行性变。此外,它还探讨了线粒体与免疫系统之间的交叉对话,强调了加剧神经元损伤的复杂相互作用。了解 mtDAMPs 的作用可以为旨在调节神经炎症和减缓疾病进展的新型疗法铺平道路,最终改善患者的预后。
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Mitochondrial DAMPs: Key Mediators in Neuroinflammation and Neurodegenerative Disease Pathogenesis.

Neurodegenerative diseases such as Alzheimer's disease (AD), Parkinson's disease (PD), Huntington's disease (HD), and amyotrophic lateral sclerosis (ALS) are increasingly linked to mitochondrial dysfunction and neuroinflammation. Central to this link are mitochondrial damage-associated molecular patterns (mtDAMPs), including mitochondrial DNA, ATP, and reactive oxygen species, released during mitochondrial stress or damage. These mtDAMPs activate inflammatory pathways, such as the NLRP3 inflammasome and cGAS-STING, contributing to the progression of neurodegenerative diseases. This review delves into the mechanisms by which mtDAMPs drive neuroinflammation and discusses potential therapeutic strategies targeting these pathways to mitigate neurodegeneration. Additionally, it explores the cross-talk between mitochondria and the immune system, highlighting the complex interplay that exacerbates neuronal damage. Understanding the role of mtDAMPs could pave the way for novel treatments aimed at modulating neuroinflammation and slowing disease progression, ultimately improving patient outcome.

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来源期刊
Neuropharmacology
Neuropharmacology 医学-神经科学
CiteScore
10.00
自引率
4.30%
发文量
288
审稿时长
45 days
期刊介绍: Neuropharmacology publishes high quality, original research and review articles within the discipline of neuroscience, especially articles with a neuropharmacological component. However, papers within any area of neuroscience will be considered. The journal does not usually accept clinical research, although preclinical neuropharmacological studies in humans may be considered. The journal only considers submissions in which the chemical structures and compositions of experimental agents are readily available in the literature or disclosed by the authors in the submitted manuscript. Only in exceptional circumstances will natural products be considered, and then only if the preparation is well defined by scientific means. Neuropharmacology publishes articles of any length (original research and reviews).
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