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中华神经创伤外科电子杂志 ›› 2026, Vol. 12 ›› Issue (01) : 52 -56. doi: 10.3877/cma.j.issn.2095-9141.2026.01.008

综述

miRNAs通过NF-κB信号通路调节炎症反应影响脊髓损伤预后的研究进展
刘晨龙1, 肖以磊2, 邢晓辉2, 李学元2,()   
  1. 1261053 山东潍坊,山东第二医科大学临床医学院
    2252000 山东聊城,聊城市人民医院神经外科
  • 收稿日期:2025-03-02 出版日期:2026-02-15
  • 通信作者: 李学元

Research progress of miRNAs in modulating inflammatory responses via the NF-κB pathway to implicate for spinal cord injury prognosis

Chenlong Liu1, Yilei Xiao2, Xiaohui Xing2, Xueyuan Li2,()   

  1. 1School of Clinical Medicine, Shandong Second Medical University, Weifang 261053, China
    2Department of Neurosurgery, Liaocheng People's Hospital, Liaocheng 252000, China
  • Received:2025-03-02 Published:2026-02-15
  • Corresponding author: Xueyuan Li
  • Supported by:
    Taishan Scholar Project of Shandong Province(202103200)
引用本文:

刘晨龙, 肖以磊, 邢晓辉, 李学元. miRNAs通过NF-κB信号通路调节炎症反应影响脊髓损伤预后的研究进展[J/OL]. 中华神经创伤外科电子杂志, 2026, 12(01): 52-56.

Chenlong Liu, Yilei Xiao, Xiaohui Xing, Xueyuan Li. Research progress of miRNAs in modulating inflammatory responses via the NF-κB pathway to implicate for spinal cord injury prognosis[J/OL]. Chinese Journal of Neurotraumatic Surgery(Electronic Edition), 2026, 12(01): 52-56.

脊髓损伤(SCI)是神经外科的常见疾病,目前临床治疗手段(如手术解压、高压氧治疗)存在局限性,难以突破疗效瓶颈。微小核糖核酸(miRNAs)可调控炎症反应、神经元凋亡和轴突再生,给SCI的治疗提供了新思路,现已成为目前神经外科领域研究的热点之一。但miRNAs具有个体差异性、自身及靶点多样性,通过调控炎症反应作用于SCI的具体机制尚不明确。基于此,本文主要围绕miRNAs通过核转录因子κB(NF-κB)通路调控小胶质细胞表型及SCI炎症微环境等方面展开综述,探讨不同的miRNAs作用于SCI的NF-κB信号通路及其下游靶点的研究进展,旨在为SCI的治疗策略提供新的研究思路及潜在靶点。

Spinal cord injury (SCI) is a common disease in Neurosurgery, and current clinical treatment methods (such as surgical decompression and hyperbaric oxygen therapy) have limitations, making it difficult to break through the therapeutic bottleneck. In recent years, the emergence of microRNAs (miRNAs) has provided new therapeutic approaches for SCI by modulating inflammatory responses, neuronal apoptosis, and axonal regeneration, making them a hotpoint in neurosurgical research. However, due to the individual variability of miRNAs and their own diversity and target diversity, the specific mechanism by which they act on SCI by regulating inflammatory responses is still unclear. Therefore this study mainly focuses on the regulation of microglial phenotype and SCI inflammatory microenvironment by miRNAs through the nuclear factor κB (NF-κB) pathway, and explores the research progress of different miRNAs acting on the NF-κB signaling pathway and downstream targets of SCI, aiming to provide new research ideas and potential targets for the treatment strategy of SCI.

[1]
Singh A, Tetreault L, Kalsi-Ryan S, et al. Global prevalence and incidence of traumatic spinal cord injury[J]. Clin Epidemiol, 2014, 6: 309-331. DOI: 10.2147/clep.S68889.
[2]
Hagen EM, Rekand T, Gilhus NE, et al. Traumatic spinal cord injuries: incidence, mechanisms and course[J]. Tidsskr Nor Laegeforen, 2012, 132(7): 831-837. DOI: 10.4045/tidsskr.10.0859.
[3]
Barbiellini Amidei C, Salmaso L, Bellio S, et al. Epidemiology of traumatic spinal cord injury: a large population-based study[J]. Spinal Cord, 2022, 60(9): 812-819. DOI: 10.1038/s41393-022-00795-w.
[4]
Ding W, Hu S, Wang P, et al. Spinal cord injury: the global incidence, prevalence, and disability from the global burden of disease study 2019[J]. Spine (Phila Pa 1976), 2022, 47(21): 1532-1540. DOI: 10.1097/brs.0000000000004417.
[5]
McDonald JW, Sadowsky C. Spinal-cord injury[J]. Lancet, 2002, 359(9304): 417-425. DOI: 10.1016/s0140-6736(02)07603-1.
[6]
Quadri SA, Farooqui M, Ikram A, et al. Recent update on basic mechanisms of spinal cord injury[J]. Neurosurg Rev, 2020, 43(2): 425-441. DOI: 10.1007/s10143-018-1008-3.
[7]
Ahuja CS, Nori S, Tetreault L, et al. Traumatic spinal cord injury-repair and regeneration[J]. Neurosurgery, 2017, 80(3s): S9-S22. DOI: 10.1093/neuros/nyw080.
[8]
Anwar MA, Al Shehabi TS, Eid AH. Inflammogenesis of secondary spinal cord injury[J]. Front Cell Neurosci, 2016, 10: 98. DOI: 10.3389/fncel.2016.00098.
[9]
郭莉丽,高谋,徐如祥.脊髓损伤的治疗新进展[J].中华神经创伤外科电子杂志, 2023, 9(6): 321-324. DOI: 10.3877/cma.j.issn.2095-9141.2023.06.001.
[10]
Hellenbrand DJ, Quinn CM, Piper ZJ, et al. Inflammation after spinal cord injury: a review of the critical timeline of signaling cues and cellular infiltration[J]. J Neuroinflammation, 2021, 18(1): 284. DOI: 10.1186/s12974-021-02337-2.
[11]
Liu X, Zhang Y, Wang Y, et al. Inflammatory response to spinal cord injury and its treatment[J]. World Neurosurg, 2021, 155: 19-31. DOI: 10.1016/j.wneu.2021.07.148.
[12]
Ge X, Zhou Z, Yang S, et al. Exosomal USP13 derived from microvascular endothelial cells regulates immune microenvironment and improves functional recovery after spinal cord injury by stabilizing IκBα[J]. Cell Biosci, 2023, 13(1): 55. DOI: 10.1186/s13578-023-01011-9.
[13]
Fan B, Wei Z, Yao X, et al. Microenvironment imbalance of spinal cord injury[J]. Cell Transplant, 2018, 27(6): 853-866. DOI: 10.1177/0963689718755778.
[14]
Hu X, Xu W, Ren Y, et al. Spinal cord injury: molecular mechanisms and therapeutic interventions[J]. Signal Transduct Target Ther, 2023, 8(1): 245. DOI: 10.1038/s41392-023-01477-6.
[15]
Silvestro S, Mazzon E. Mirnas as promising translational strategies for neuronal repair and regeneration in spinal cord injury[J]. Cells, 2022, 11(14): 2177. DOI: 10.3390/cells11142177.
[16]
Almurshidi B, Carver W, Scott G, et al. Roles of miRNAs in spinal cord injury and potential therapeutic interventions[J]. Neuroimmunol Neuroinflamm, 2019, 6: 11. DOI: 10.20517/2347-8659.2019.19.
[17]
Zhang C, Talifu Z, Xu X, et al. MicroRNAs in spinal cord injury: a narrative review[J]. Front Mol Neurosci, 2023, 16: 1099256. DOI: 10.3389/fnmol.2023.1099256.
[18]
Deng ZZ, Chen YH. Research progress of microRNAs in spinal cord injury[J]. J Integr Neurosci, 2023, 22(2): 31. DOI: 10.31083/j.jin2202031.
[19]
Fu SP, Chen SY, Pang QM, et al. Advances in the research of the role of macrophage/microglia polarization-mediated inflammatory response in spinal cord injury[J]. Front Immunol, 2022, 13: 1014013. DOI: 10.3389/fimmu.2022.1014013.
[20]
Liu WZ, Ma ZJ, Li JR, et al. Mesenchymal stem cell-derived exosomes: therapeutic opportunities and challenges for spinal cord injury[J]. Stem Cell Res Ther, 2021, 12(1): 102. DOI: 10.1186/s13287-021-02153-8.
[21]
Akhmetzyanova E, Kletenkov K, Mukhamedshina Y, et al. Different approaches to modulation of microglia phenotypes after spinal cord injury[J]. Front Syst Neurosci, 2019, 13: 37. DOI: 10.3389/fnsys.2019.00037.
[22]
He R, Tang GL, Niu L, et al. Quietness Circ 0000962 promoted nerve cell inflammation through PIK3CA/Akt/NF-κB signaling by miR-302b-3p in spinal cord injury[J]. Ann Palliat Med, 2020, 9(2): 190-198. DOI: 10.21037/apm.2020.02.13.
[23]
Chen J, Wang Z, Zheng Z, et al. Neuron and microglia/macrophage-derived FGF10 activate neuronal FGFR2/PI3K/Akt signaling and inhibit microglia/macrophages TLR4/NF-κB-dependent neuroinflammation to improve functional recovery after spinal cord injury[J]. Cell Death Dis, 2017, 8(10): e3090. DOI: 10.1038/cddis.2017.490.
[24]
Lin ZH, Wang SY, Chen LL, et al. Methylene blue mitigates acute neuroinflammation after spinal cord injury through inhibiting NLRP3 inflammasome activation in microglia[J]. Front Cell Neurosci, 2017, 11: 391. DOI: 10.3389/fncel.2017.00391.
[25]
Tao GJ, Qian DF, Li LW, et al. Parthenolide promotes the repair of spinal cord injury by modulating M1/M2 polarization via the NF-κB and STAT 1/3 signaling pathway[J]. Cell Death Discov, 2020, 6(1): 97. DOI: 10.1038/s41420-020-00333-8.
[26]
Liu C, Hu F, Jiao G, et al. DDental pulp stem cell-derived exosomes suppress M1 macrophage polarization through the ROS-MAPK-NFκB P65 signaling pathway after spinal cord injury[J]. J Nanobiotechnology, 2022, 20(1): 65. DOI: 10.1186/s12951-022-01273-4.
[27]
Zhao H, Wang X, Liu S, et al. Paeonol regulates NLRP3 inflammasomes and pyroptosis to alleviate spinal cord injury of rat[J]. BMC Neurosci, 2022, 23(1): 16. DOI: 10.1186/s12868-022-00698-9.
[28]
Feng X, Chen X, Zaeem M, et al. Sesamol attenuates neuroinflammation by regulating the AMPK/SIRT1/NF-κB signaling pathway after spinal cord injury in mice[J]. Oxid Med Cell Longev, 2022, 2022: 8010670. DOI: 10.1155/2022/8010670.
[29]
Liang W, Han B, Hai Y, et al. The role of microglia/macrophages activation and TLR4/NF-κB/MAPK pathway in distraction spinal cord injury-induced inflammation[J]. Front Cell Neurosci, 2022, 16: 926453. DOI: 10.3389/fncel.2022.926453.
[30]
Liu NK, Wang XF, Lu QB, et al. Altered microRNA expression following traumatic spinal cord injury[J]. Exp Neurol, 2009, 219(2): 424-429. DOI: 10.1016/j.expneurol.2009.06.015.
[31]
Yuan Y, Tong L, Wu S. microRNA and NF-kappa B[J]. Adv Exp Med Biol, 2015, 887: 157-170. DOI: 10.1007/978-3-319-22380-3_9.
[32]
Zhang P, Li LQ, Zhang D, et al. Over-expressed miR-27a-3p inhibits inflammatory response to spinal cord injury by decreasing TLR4[J]. Eur Rev Med Pharmacol Sci, 2018, 22(17): 5416-5423. DOI: 10.26355/eurrev_201809_15800.
[33]
Wang B, Shen PF, Qu YX, et al. miR-940 promotes spinal cord injury recovery by inhibiting TLR4/NF-κB pathway-mediated inflammation[J]. Eur Rev Med Pharmacol Sci, 2019, 23(8): 3190-3197. DOI: 10.26355/eurrev_201904_17677.
[34]
Wang X, Yang Y, Li W, et al. Umbilical mesenchymal stem cell-derived exosomes promote spinal cord functional recovery through the miR-146b/TLR4 -mediated NF-κB p65 signaling pathway in rats[J]. Biochem Biophys Rep, 2023, 35: 101497. DOI: 10.1016/j.bbrep.2023.101497.
[35]
Jiang Z, Zhang J. Mesenchymal stem cell-derived exosomes containing miR-145-5p reduce inflammation in spinal cord injury by regulating the TLR4/NF-κB signaling pathway[J]. Cell Cycle, 2021, 20(10): 993-1009. DOI: 10.1080/15384101.2021.1919825.
[36]
Xue H, Ran B, Li J, et al. Bone marrow mesenchymal stem cell exosomes-derived microRNA-216a-5p on locomotor performance, neuronal injury, and microglia inflammation in spinal cord injury[J]. Front Cell Dev Biol, 2023, 11: 1227440. DOI: 10.3389/fcell.2023.1227440.
[37]
Lv ZC, Cao XY, Guo YX, et al. Effects of miR-146a on repair and inflammation in rats with spinal cord injury through the TLR/NF-κB signaling pathway[J]. Eur Rev Med Pharmacol Sci, 2019, 23(11): 4558-4563. DOI: 10.26355/eurrev_201906_18031.
[38]
Tan Y, Yu L, Zhang C, et al. miRNA-146a attenuates inflammation in an in vitro spinal cord injury model via inhibition of TLR4 signaling[J]. Exp Ther Med, 2018, 16(4): 3703-3709. DOI: 10.3892/etm.2018.6645.
[39]
Li XH, Fu NS, Xing ZM. MiR-100 suppresses inflammatory activation of microglia and neuronal apoptosis following spinal cord injury via TLR4/NF-κB pathway[J]. Eur Rev Med Pharmacol Sci, 2019, 23(20): 8713-8720. DOI: 10.26355/eurrev_201910_19265.
[40]
Liu W, Rong Y, Wang J, et al. Exosome-shuttled miR-216a-5p from hypoxic preconditioned mesenchymal stem cells repair traumatic spinal cord injury by shifting microglial M1/M2 polarization[J]. J Neuroinflammation, 2020, 17(1): 47. DOI: 10.1186/s12974-020-1726-7.
[41]
Fei M, Li Z, Cao Y, et al. MicroRNA-182 improves spinal cord injury in mice by modulating apoptosis and the inflammatory response via IKKβ/NF-κB[J]. Lab Invest, 2021, 101(9): 1238-1253. DOI: 10.1038/s41374-021-00606-5.
[42]
Gao F, Shen J, Zhao L, et al. Curcumin alleviates lipopolysaccharide (LPS)-activated neuroinflammation via modulation of miR-199b-5p/IκB Kinase β (IKKβ)/Nuclear Factor Kappa B (NF-κB) Pathway in Microglia[J]. Med Sci Monit, 2019, 25: 9801-9810. DOI: 10.12659/msm.918237.
[43]
Li L, Qi C, Liu Y, et al. MicroRNA miR-27b-3p regulate microglial inflammation response and cell apoptosis by inhibiting A20 (TNF-α-induced protein 3)[J]. Bioengineered, 2021, 12(2): 9902-9913. DOI: 10.1080/21655979.2021.1969195.
[44]
Li XZ, Lv CL, Shi JG, et al. MiR-543-3p promotes locomotor function recovery after spinal cord injury by inhibiting the expression of tumor necrosis factor superfamily member 15 in rats[J]. Eur Rev Med Pharmacol Sci, 2019, 23(7): 2701-2709. DOI: 10.26355/eurrev_201904_17540.
[45]
Zhou X, Chen J, Zhang H, et al. MicroRNA-23b attenuates the H2O2-induced injury of microglial cells via TAB3/NF-κB signaling pathway[J]. Int J Clin Exp Pathol, 2018, 11(12): 5765-5773.
[46]
Sun F, Li SG, Zhang HW, et al. MiRNA-411 attenuates inflammatory damage and apoptosis following spinal cord injury[J]. Eur Rev Med Pharmacol Sci, 2020, 24(2): 491-498. DOI: 10.26355/eurrev_202001_20022.
[47]
Jiang D, Gong F, Ge X, et al. Neuron-derived exosomes-transmitted miR-124-3p protect traumatically injured spinal cord by suppressing the activation of neurotoxic microglia and astrocytes[J]. J Nanobiotechnology, 2020, 18(1): 105. DOI: 10.1186/s12951-020-00665-8.
[48]
Jia D, Niu Y, Li D, et al. MicroRNA-223 alleviates lipopolysaccharide-induced PC-12 cells apoptosis and autophagy by targeting RPH1 in spinal cord injury[J]. Int J Clin Exp Pathol, 2017, 10(9): 9223-9232.
[49]
Sha W, Zhang X, Zhou Z, et al. The inhibition of microRNA-31 weakens acute spinal cord injury through nuclear factor-κB and TGF-β/Smad 2 in rat[J]. Int J Clin Exp Pathol, 2017, 10(9): 9122-9131.
[50]
Deng G, Gao Y, Cen Z, et al. miR-136-5p regulates the inflammatory response by targeting the IKKβ/NF-κB/A20 pathway after spinal cord injury[J]. Cell Physiol Biochem, 2018, 50(2): 512-524. DOI: 10.1159/000494165.
[51]
Diener C, Keller A, Meese E. Emerging concepts of miRNA therapeutics: from cells to clinic[J]. Trends Genet, 2022, 38(6): 613-626. DOI: 10.1016/j.tig.2022.02.006.
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