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微小RNA-124:神经疾病中小胶质细胞介导的炎症反应中的关键因子

MicroRNA-124: A Key Player in Microglia-Mediated Inflammation in Neurological Diseases.

作者信息

Zhao Jiuhan, He Zhenwei, Wang Jialu

机构信息

Department of Neurology, First Affiliated Hospital of China Medical University, Shenyang, China.

Department of Neurology, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.

出版信息

Front Cell Neurosci. 2021 Nov 2;15:771898. doi: 10.3389/fncel.2021.771898. eCollection 2021.

DOI:10.3389/fncel.2021.771898
PMID:34795564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8593194/
Abstract

Neurological disorders are mainly characterized by progressive neuron loss and neurological deterioration, which cause human disability and death. However, many types of neurological disorders have similar pathological mechanisms, including the neuroinflammatory response. Various microRNAs (miRs), such as miR-21, miR-124, miR-146a, and miR-132 were recently shown to affect a broad spectrum of biological functions in the central nervous system (CNS). Microglia are innate immune cells with important roles in the physiological and pathological activities of the CNS. Recently, abnormal expression of miR-124 was shown to be associated with the occurrence and development of various diseases in CNS via regulating microglia function. In addition, miR-124 is a promising biomarker and therapeutic target. Studies on the role of miR-124 in regulating microglia function involved in pathogenesis of neurological disorders at different stages will provide new ideas for the use of miR-124 as a therapeutic target for different CNS diseases.

摘要

神经疾病主要以进行性神经元丧失和神经功能恶化为特征,这会导致人类残疾和死亡。然而,许多类型的神经疾病具有相似的病理机制,包括神经炎症反应。最近研究表明,多种微小RNA(miR),如miR-21、miR-124、miR-146a和miR-132,会影响中枢神经系统(CNS)的广泛生物学功能。小胶质细胞是先天性免疫细胞,在中枢神经系统的生理和病理活动中发挥重要作用。最近研究表明,miR-124的异常表达通过调节小胶质细胞功能与中枢神经系统各种疾病的发生和发展相关。此外,miR-124是一种有前景的生物标志物和治疗靶点。研究miR-124在不同阶段调节参与神经疾病发病机制的小胶质细胞功能中的作用,将为把miR-124用作不同中枢神经系统疾病的治疗靶点提供新思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b92/8593194/83ac8028a097/fncel-15-771898-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b92/8593194/83ac8028a097/fncel-15-771898-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b92/8593194/83ac8028a097/fncel-15-771898-g001.jpg

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本文引用的文献

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Cells. 2021 Aug 12;10(8):2066. doi: 10.3390/cells10082066.
2
Expression of miR-1-3p, miR-16-5p and miR-122-5p as Possible Risk Factors of Secondary Cardiovascular Events.miR-1-3p、miR-16-5p和miR-122-5p的表达作为继发性心血管事件的潜在危险因素
Biomedicines. 2021 Aug 20;9(8):1055. doi: 10.3390/biomedicines9081055.
3
M2 microglial small extracellular vesicles reduce glial scar formation the miR-124/STAT3 pathway after ischemic stroke in mice.
Exosome-powered neuropharmaceutics: unlocking the blood-brain barrier for next-gen therapies.
外泌体驱动的神经药物:为下一代疗法开启血脑屏障。
J Nanobiotechnology. 2025 May 3;23(1):329. doi: 10.1186/s12951-025-03352-8.
4
Integrated transcriptomics of multiple sclerosis peripheral blood mononuclear cells explored potential biomarkers for the disease.多发性硬化症外周血单个核细胞的综合转录组学研究探索了该疾病的潜在生物标志物。
Biochem Biophys Rep. 2025 Apr 18;42:102022. doi: 10.1016/j.bbrep.2025.102022. eCollection 2025 Jun.
5
Alterations of circulating exosomal microRNAs in an LPS-induced depression model of male mice: Potential role in the anti-depressive effects of acupuncture.脂多糖诱导的雄性小鼠抑郁模型中循环外泌体微小RNA的变化:针刺抗抑郁作用的潜在机制
Physiol Rep. 2025 Apr;13(7):e70310. doi: 10.14814/phy2.70310.
6
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Cells. 2025 Mar 12;14(6):421. doi: 10.3390/cells14060421.
7
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Front Oncol. 2025 Mar 10;15:1534862. doi: 10.3389/fonc.2025.1534862. eCollection 2025.
8
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J Nanobiotechnology. 2024 Dec 2;22(1):747. doi: 10.1186/s12951-024-03019-w.
9
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Stem Cell Rev Rep. 2025 Jan;21(1):236-253. doi: 10.1007/s12015-024-10803-6. Epub 2024 Nov 6.
10
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Aging Cell. 2025 Feb;24(2):e14393. doi: 10.1111/acel.14393. Epub 2024 Oct 25.
M2 小胶质细胞外囊泡通过 miR-124/STAT3 通路减少缺血性脑卒中后小鼠的神经胶质瘢痕形成。
Theranostics. 2021 Jan 1;11(3):1232-1248. doi: 10.7150/thno.48761. eCollection 2021.
4
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Ann Clin Transl Neurol. 2020 Sep;7(9):1594-1607. doi: 10.1002/acn3.51146. Epub 2020 Aug 29.
5
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Int J Mol Sci. 2020 Jul 29;21(15):5381. doi: 10.3390/ijms21155381.
6
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J Nanobiotechnology. 2020 Jul 25;18(1):105. doi: 10.1186/s12951-020-00665-8.
7
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J Neuroinflammation. 2020 Jul 14;17(1):209. doi: 10.1186/s12974-020-01882-6.
8
MicroRNA alterations in neuropathologic cognitive disorders with an emphasis on dementia: Lessons from animal models.神经病理认知障碍中微小 RNA 的改变,重点是痴呆症:来自动物模型的教训。
J Cell Physiol. 2021 Feb;236(2):806-823. doi: 10.1002/jcp.29908. Epub 2020 Jun 30.
9
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Front Mol Neurosci. 2020 Jun 5;13:90. doi: 10.3389/fnmol.2020.00090. eCollection 2020.
10
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Brain Inj. 2020 Jun 6;34(7):965-974. doi: 10.1080/02699052.2020.1764102. Epub 2020 Jun 4.