cGAS-STING信号通路参与阿尔茨海默病的研究进展
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河南中医药大学第一附属医院

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国家科技重大专项;河南省博士后基金项目;河南省医学科技攻关计划省部共建项目;河南省科技发展计划项目;河南省卫生健康委国家中医药传承创新中心科研专项


Research Progress on the cGAS-STING Signalling Pathway in Alzheimer's Disease
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First Affiliated Hospital,Henan University of Chinese Medicine

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National Major Science and Technology Projects; Henan Provincial Postdoctoral Research Fund Programme; Henan Provincial Medical Science and Technology Research Programme: Provincial-Ministerial Jointly-Established Project; Henan Provincial Science and Technology Development Programme Project; Research Project of the National Centre for the Inheritance and Innovation of Traditional Chinese Medicine, Henan Provincial Health Commission

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    摘要:

    阿尔茨海默病(Alzheimer's disease,AD)是一种以认知功能障碍和执行功能损害为主的神经退行性疾病。作为至关重要的先天免疫通路,环磷酸鸟苷-磷酸腺苷合成酶(cyclic GMP-AMP synthase,cGAS)-干扰素基因刺激因子(stimulator of interferon genes,STING)信号通路在AD中的异常激活备受关注。本文讨论了cGAS-STING信号通路通过β-淀粉样蛋白(β-amyloid,Aβ)沉积和异常Tau蛋白聚集、氧化应激与线粒体功能障碍、神经炎症和神经胶质细胞异常、突触功能障碍、血管功能障碍、肠道菌群失调、自噬功能障碍等机制参与AD以及干预cGAS-STING信号通路治疗AD的相关研究,旨在揭示cGAS-STING信号通路的异常激活可能是AD发病的重要原因之一,并有望成为治疗AD的潜在干预靶点。

    Abstract:

    Alzheimer's disease(AD) is a neurodegenerative disorder characterized primarily by cognitive impairment and executive function deficits. As a crucial innate immune pathway, the abnormal activation of the cyclic GMP-AMP synthase-stimulator of interferon gene(cGAS-STING) signaling pathway in AD has drawn significant attention. This paper discusses the involvement of the cGAS-STING signalling pathway in Alzheimer's disease (AD) through mechanisms including Aβ deposition and abnormal Tau protein aggregation, oxidative stress and mitochondrial dysfunction, neuroinflammation and glial cell abnormalities, synaptic dysfunction, vascular dysfunction, gut microbiota dysbiosis, and autophagy dysfunction, as well as relevant research on intervening in the cGAS-STING signalling pathway for the treatment of AD.The aim is to reveal that the abnormal activation of the cGAS-STING signaling pathway is a significant cause of AD pathogenesis and may serve as a potential intervention target for the treatment of AD.

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  • 收稿日期:2025-10-28
  • 最后修改日期:2026-01-08
  • 录用日期:2026-03-09
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