Suppr超能文献

软骨终板炎症所致椎间盘退变的发病机制及靶向治疗

The pathogenesis and targeted therapies of intervertebral disc degeneration induced by cartilage endplate inflammation.

作者信息

Yang Hantao, Chen Xuandu, Chen Jun, Dong Yansong, Huang Yafang, Qin Lei, Tan Jie, Yi Weihong

机构信息

Department of Spine Surgery and Innovative Laboratory of Orthopedics, Shenzhen Nanshan People's Hospital, Shenzhen, Guangdong, China.

Orthopedic Laboratory, Orthopedic Department and Hubei Sports Medicine Center, Wuhan Fourth Hospital, Wuhan, China.

出版信息

Front Cell Dev Biol. 2024 Dec 2;12:1492870. doi: 10.3389/fcell.2024.1492870. eCollection 2024.

Abstract

Intervertebral disc degeneration (IVDD) is the leading cause of low back pain, where degeneration and death of nucleus pulposus cells within the intervertebral disc (IVD) can be obviously revealed. This degeneration can result in an imbalance in the extracellular matrix due to the loss of proteoglycans and water content, which can further lead to catabolic and anabolic dysfunction of the IVD. Recently, the dysfunction of cartilage endplate (CEP) during aging has drawn large attention due to its essential functions in contributing nutrient exchange and maintaining IVD homeostasis. Furthermore, the inflammation and disturbed homeostasis of CEP not only accelerate the degradation of nucleus pulposus extracellular matrix, but also exacerbate IVDD by causing nucleus pulposus cell death through other pathological factors. Here in this review, we summarized the possible pathological factors and the underlying mechanisms of the CEP inflammation-induced IVDD, including exosomes degeneration, CEP calcification, ferroptosis, mechanical changes, and cell senescence. Besides, changes of miRNAs, pain-related neural reflex arc and pathways associated with CEP inflammation-induced IVDD are also reviewed. In addition, new strategies specifically designed for CEP inflammation-induced IVDD are also discussed in the last section. We hope this paper can not only offer some new insights for advancing novel strategies for treating IVDD, but also serve as a valuable reference for researchers in this field.

摘要

椎间盘退变(IVDD)是腰痛的主要原因,其中椎间盘(IVD)内髓核细胞的退变和死亡可明显显现。这种退变会因蛋白聚糖和水分含量的丧失导致细胞外基质失衡,进而导致IVD的分解代谢和合成代谢功能障碍。近年来,软骨终板(CEP)在衰老过程中的功能障碍因其在营养物质交换和维持IVD内环境稳态中的重要作用而备受关注。此外,CEP的炎症和内环境稳态紊乱不仅加速了髓核细胞外基质的降解,还通过其他病理因素导致髓核细胞死亡,从而加剧IVDD。在本综述中,我们总结了CEP炎症诱导IVDD的可能病理因素及潜在机制,包括外泌体退变、CEP钙化、铁死亡、力学变化和细胞衰老。此外,还综述了与CEP炎症诱导IVDD相关的miRNA变化、疼痛相关神经反射弧及信号通路。此外,最后一部分还讨论了专门针对CEP炎症诱导IVDD的新策略。我们希望本文不仅能为推进IVDD治疗新策略提供一些新见解,也能为该领域的研究人员提供有价值的参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9072/11647014/a385e44aba62/fcell-12-1492870-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验