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去氢木香内酯通过抑制STING-TBK1/NF-κB和MAPK信号通路减轻髓核细胞衰老并改善椎间盘退变。

Dehydrocostus Lactone Attenuates the Senescence of Nucleus Pulposus Cells and Ameliorates Intervertebral Disc Degeneration via Inhibition of STING-TBK1/NF-κB and MAPK Signaling.

作者信息

Chen Zhiqian, Yang Xiao, Zhou Yifan, Liang Zhihao, Chen Chen, Han Chen, Cao Xiankun, He Wenxin, Zhang Kai, Qin An, Zhou Tangjun, Zhao Jie

机构信息

Shanghai Key Laboratory of Orthopaedic Implant, Shanghai Ninth People's Hospital, Shanghai, China.

Department of Orthopedics, Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.

出版信息

Front Pharmacol. 2021 Apr 14;12:641098. doi: 10.3389/fphar.2021.641098. eCollection 2021.

DOI:10.3389/fphar.2021.641098
PMID:33935734
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8079987/
Abstract

The progression of intervertebral disc degeneration (IDD) is multifactorial with the senescence of nucleus pulposus (NP) cells and closely related to inflammation in NP cells. Dehydrocostus lactone (DHE) is a natural sesquiterpene lactone isolated from medicinal plants that has anti-inflammatory properties. Thus, DHE may have a therapeutic effect on the progression of IDD. In this study, NP cells were used to determine the appropriate concentration of DHE . The role of DHE in tumor necrosis factor-α (TNF-α)-induced activation of inflammatory signaling pathways and cellular senescence, together with anabolism and catabolism of extracellular matrix (ECM) in NP cells, was examined . The therapeutic effect of DHE was determined using a spinal instability model of IDD in mice. The TNF-α-induced ECM degradation and the senescence of NP cells were partially attenuated by DHE. Mechanistically, DHE inhibited the activation of NF-κB and MAPK inflammatory signaling pathways and ameliorated the senescence of NP cells caused by the activation of STING-TBK1/NF-κB signaling induced by TNF-α. Furthermore, a spinal instability model in mice demonstrated that DHE treatment could ameliorate progression of IDD. Together, our findings indicate that DHE can alleviate IDD changes and has a potential therapeutic function for the treatment of IDD.

摘要

椎间盘退变(IDD)的进展是多因素的,与髓核(NP)细胞的衰老有关,并且与NP细胞中的炎症密切相关。脱氢木香内酯(DHE)是一种从具有抗炎特性的药用植物中分离出的天然倍半萜内酯。因此,DHE可能对IDD的进展具有治疗作用。在本研究中,使用NP细胞来确定DHE的合适浓度。研究了DHE在肿瘤坏死因子-α(TNF-α)诱导的炎症信号通路激活和细胞衰老以及NP细胞中细胞外基质(ECM)合成代谢和分解代谢中的作用。使用小鼠IDD的脊柱不稳定模型确定DHE的治疗效果。DHE部分减轻了TNF-α诱导的ECM降解和NP细胞衰老。机制上,DHE抑制NF-κB和MAPK炎症信号通路的激活,并改善了由TNF-α诱导的STING-TBK1/NF-κB信号激活引起的NP细胞衰老。此外,小鼠脊柱不稳定模型表明DHE治疗可以改善IDD的进展。总之,我们的研究结果表明DHE可以减轻IDD变化,对IDD的治疗具有潜在的治疗作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0500/8079987/1a0e8007af5e/fphar-12-641098-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0500/8079987/f126070385f3/fphar-12-641098-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0500/8079987/f126070385f3/fphar-12-641098-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0500/8079987/2da7b5884cda/fphar-12-641098-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0500/8079987/87ee77fbef05/fphar-12-641098-g003.jpg
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本文引用的文献

1
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Biomed Pharmacother. 2020 Nov;131:110660. doi: 10.1016/j.biopha.2020.110660. Epub 2020 Aug 24.
2
Molecular mechanisms and cellular functions of cGAS-STING signalling.cGAS-STING 信号转导的分子机制和细胞功能。
Nat Rev Mol Cell Biol. 2020 Sep;21(9):501-521. doi: 10.1038/s41580-020-0244-x. Epub 2020 May 18.
3
TBK1 and IKKε Act Redundantly to Mediate STING-Induced NF-κB Responses in Myeloid Cells.TBK1 和 IKKε 冗余性地介导 STING 诱导的髓系细胞中的 NF-κB 反应。
控释褪黑素纳米颗粒促进髓核细胞稳态的恢复以减轻椎间盘退变。
Mater Today Bio. 2025 Jun 16;33:101994. doi: 10.1016/j.mtbio.2025.101994. eCollection 2025 Aug.
4
Exploring the Causes of Intervertebral Disc Annulus Fibrosus Impairment.探索椎间盘纤维环损伤的原因。
Cell Mol Bioeng. 2025 Mar 16;18(2):109-121. doi: 10.1007/s12195-025-00844-3. eCollection 2025 Apr.
5
Homoplantaginin exerts therapeutic effects on intervertebral disc degeneration by alleviating TNF-α-induced nucleus pulposus cell senescence and inflammation.高车前素通过减轻肿瘤坏死因子-α诱导的髓核细胞衰老和炎症,对椎间盘退变发挥治疗作用。
Front Pharmacol. 2025 Mar 27;16:1526107. doi: 10.3389/fphar.2025.1526107. eCollection 2025.
6
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Cell Rep. 2020 Apr 7;31(1):107492. doi: 10.1016/j.celrep.2020.03.056.
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5
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6
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DNA Repair (Amst). 2019 Nov;83:102673. doi: 10.1016/j.dnarep.2019.102673. Epub 2019 Jul 25.
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