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细胞焦亡与椎间盘退变:机制洞察与治疗意义

Pyroptosis and Intervertebral Disc Degeneration: Mechanistic Insights and Therapeutic Implications.

作者信息

Ge Yuying, Chen Yuying, Guo Chijiao, Luo Huan, Fu Fangda, Ji Weifeng, Wu Chengliang, Ruan Hongfeng

机构信息

The First Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou, 310053, People's Republic of China.

The Fourth Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, People's Republic of China.

出版信息

J Inflamm Res. 2022 Oct 17;15:5857-5871. doi: 10.2147/JIR.S382069. eCollection 2022.


DOI:10.2147/JIR.S382069
PMID:36263145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9575467/
Abstract

Low back pain (LBP) is a common problem worldwide, resulting in great patient suffering and great challenges for the social health system. Intervertebral disc (IVD) degeneration (IVDD) is widely acknowledged as one of the key causes of LBP. Accumulating evidence suggests that aberrant pyroptosis of IVD cells is involved in the pathogenesis of IVDD progression, however, the comprehensive roles of pyroptosis in IVDD have not been fully established, leaving attempts to treat IVDD with anti-pyroptosis approaches questionable. In this review, we summarize the characteristics of pyroptosis and emphasize the effects of IVD cell pyroptosis on the pathological progression of IVDD, including secretion of cytokines, nucleus pulposus cell apoptosis and autophagy, accelerated extracellular matrix degradation, annulus fibrosus rupture, cartilage endplate calcification, vascularization, sensory and sympathetic fiber neoinnervation, and infiltrating lymphatic vessels. Finally, we discuss several interventions used to treat IVDD by targeting pyroptosis. This review provides novel insights into the crucial role of IVD cell pyroptosis in IVDD pathogenesis, and could be informative for developing novel therapeutic approaches for IVDD and LBP.

摘要

下腰痛(LBP)是全球范围内的常见问题,给患者带来巨大痛苦,也给社会卫生系统带来巨大挑战。椎间盘(IVD)退变(IVDD)被广泛认为是LBP的主要原因之一。越来越多的证据表明,IVD细胞异常焦亡参与了IVDD进展的发病机制,然而,焦亡在IVDD中的综合作用尚未完全明确,因此用抗焦亡方法治疗IVDD的尝试存在疑问。在本综述中,我们总结了焦亡的特征,并强调了IVD细胞焦亡对IVDD病理进展的影响,包括细胞因子分泌、髓核细胞凋亡和自噬、细胞外基质降解加速、纤维环破裂、软骨终板钙化、血管生成、感觉和交感神经纤维新生以及淋巴管浸润。最后,我们讨论了几种通过靶向焦亡来治疗IVDD的干预措施。本综述为IVD细胞焦亡在IVDD发病机制中的关键作用提供了新的见解,并可能为开发治疗IVDD和LBP的新方法提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a67f/9575467/2939ed5f88f8/JIR-15-5857-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a67f/9575467/8dc64097d8c8/JIR-15-5857-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a67f/9575467/2939ed5f88f8/JIR-15-5857-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a67f/9575467/8dc64097d8c8/JIR-15-5857-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a67f/9575467/2939ed5f88f8/JIR-15-5857-g0002.jpg

相似文献

[1]
Pyroptosis and Intervertebral Disc Degeneration: Mechanistic Insights and Therapeutic Implications.

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[2]
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引用本文的文献

[1]
Ipriflavone ameliorates intervertebral disc degeneration by inhibiting osteoporosis of vertebral body and pyroptosis of the nucleus pulposus in instability of lumbar spine and diabetic mice.

Front Bioeng Biotechnol. 2025-8-5

[2]
Subchronic Chlorpyrifos Exposure Induces Thyroid Follicular Cell Pyroptosis to Exacerbate Thyroid Toxicity by Modulating Nrf2/Keap1/NF-κB Pathway in Male Mice.

J Inflamm Res. 2025-7-15

[3]
Potential diagnostic and therapeutic gene in chronic low back pain through pyroptosis modulation: A silico study based on the dataset analysis.

Sci Rep. 2025-7-16

[4]
Single nuclear-spatial transcriptomic sequencing reveals distinct puncture-induced cell subpopulations in the intervertebral disc of a rat model.

Clin Transl Med. 2025-6

[5]
Exploring extracellular vesicles as novel therapeutic agents for intervertebral disc degeneration: delivery, applications, and mechanisms.

Stem Cell Res Ther. 2025-5-1

[6]
Novel anti-pyroptosis drug loaded on metal-organic framework for intervertebral disc degeneration therapy.

Mater Today Bio. 2025-4-5

[7]
Mechanism of lncRNA ZFAS1 mediating nucleus pulposus cell pyroptosis in intervertebral disc degeneration.

J Orthop Surg Res. 2025-2-25

[8]
Pyroptosis: candidate key targets for mesenchymal stem cell-derived exosomes for the treatment of bone-related diseases.

Stem Cell Res Ther. 2025-2-12

[9]
Gene-Silencing Therapeutic Approaches Targeting PI3K/Akt/mTOR Signaling in Degenerative Intervertebral Disk Cells: An In Vitro Comparative Study Between RNA Interference and CRISPR-Cas9.

Cells. 2024-12-9

[10]
Integrating bioinformatics and experimental validation to Investigate IRF1 as a novel biomarker for nucleus pulposus cells necroptosis in intervertebral disc degeneration.

Sci Rep. 2024-12-3

本文引用的文献

[1]
Iron overload promotes intervertebral disc degeneration via inducing oxidative stress and ferroptosis in endplate chondrocytes.

Free Radic Biol Med. 2022-9

[2]
MiR-1656 targets GPX4 to trigger pyroptosis in broilers kidney tissues by activating NLRP3 inflammasome under Se deficiency.

J Nutr Biochem. 2022-7

[3]
α-Mangostin protects lipopolysaccharide-stimulated nucleus pulposus cells against NLRP3 inflammasome-mediated apoptosis via the NF-κB pathway.

J Appl Toxicol. 2022-9

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Targeting Cell Death: Pyroptosis, Ferroptosis, Apoptosis and Necroptosis in Osteoarthritis.

Front Cell Dev Biol. 2022-1-18

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Kindlin-2 reduces IVD inflammation.

Nat Rev Rheumatol. 2022-3

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Kindlin-2 inhibits Nlrp3 inflammasome activation in nucleus pulposus to maintain homeostasis of the intervertebral disc.

Bone Res. 2022-1-10

[7]
Panax notoginseng saponins attenuate intervertebral disc degeneration by reducing the end plate porosity in lumbar spinal instability mice.

JOR Spine. 2021-11-30

[8]
Moderate-intensity exercise alleviates pyroptosis by promoting autophagy in osteoarthritis via the P2X7/AMPK/mTOR axis.

Cell Death Discov. 2021-11-10

[9]
MicroRNA‑200c‑3p suppresses intervertebral disc degeneration by targeting RAP2C/ERK signaling.

Mol Med Rep. 2021-12

[10]
Notoginsenoside R1 suppresses inflammatory response and the pyroptosis of nucleus pulposus cells via inactivating NF-κB/NLRP3 pathways.

Int Immunopharmacol. 2021-12

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