Zhou Daqian, Mei Yongliang, Song Chao, Cheng Kang, Cai Weiye, Guo Daru, Gao Silong, Lv Jiale, Liu Tao, Zhou Yang, Wang Liquan, Liu Bing, Liu Zongchao
Department of Orthopedics, The Affiliated Traditional Chinese Medicine Hospital, Southwest Medical University, Luzhou, Sichuan Province, China.
Luzhou Longmatan District People's Hospital, Luzhou, Sichuan, China.
Eur J Clin Invest. 2024 Sep;54(9):e14226. doi: 10.1111/eci.14226. Epub 2024 Apr 17.
Intervertebral disc degeneration (IVDD) is a common chronic orthopaedic disease in orthopaedics that imposes a heavy economic burden on people and society. Although it is well established that IVDD is associated with genetic susceptibility, ageing and obesity, its pathogenesis remains incompletely understood. Previously, IVDD was thought to occur because of excessive mechanical loading leading to destruction of nucleus pulposus cells (NPCs), but studies have shown that IVDD is a much more complex process associated with inflammation, metabolic factors and NPCs death and can involve all parts of the disc, characterized by causing NPCs death and extracellular matrix (ECM) degradation. The damage pattern of NPCs in IVDD is like that of some programmed cell death, suggesting that IVDD is associated with programmed cell death. Although apoptosis and pyroptosis of NPCs have been studied in IVDD, the pathogenesis of intervertebral disc degeneration can still not be fully elucidated by using only traditional cell death modalities. With increasing research, some new modes of cell death, PANoptosis, ferroptosis and senescence have been found to be closely related to intervertebral disc degeneration. Among these, PANoptosis combines essential elements of pyroptosis, apoptosis and necroptosis to form a highly coordinated and dynamically balanced programmed inflammatory cell death process. Furthermore, we believe that PANoptosis may also crosstalk with pyroptosis and senescence. Therefore, we review the progress of research on multiple deaths of NPCs in IVDD to provide guidance for clinical treatment.
椎间盘退变(IVDD)是骨科常见的慢性疾病,给个人和社会带来沉重的经济负担。尽管IVDD与遗传易感性、衰老和肥胖有关已得到充分证实,但其发病机制仍未完全明确。以前,人们认为IVDD是由于过度的机械负荷导致髓核细胞(NPCs)破坏而发生的,但研究表明,IVDD是一个更为复杂的过程,与炎症、代谢因素以及NPCs死亡有关,可累及椎间盘的各个部分,其特征是导致NPCs死亡和细胞外基质(ECM)降解。IVDD中NPCs的损伤模式类似于某些程序性细胞死亡,这表明IVDD与程序性细胞死亡有关。尽管在IVDD中已经对NPCs的凋亡和焦亡进行了研究,但仅使用传统的细胞死亡方式仍无法完全阐明椎间盘退变的发病机制。随着研究的不断深入,发现一些新的细胞死亡模式,如PANoptosis、铁死亡和衰老与椎间盘退变密切相关。其中,PANoptosis结合了焦亡、凋亡和坏死性凋亡的基本要素,形成了一个高度协调且动态平衡的程序性炎症细胞死亡过程。此外,我们认为PANoptosis也可能与焦亡和衰老相互作用。因此,我们综述了IVDD中NPCs多种死亡方式的研究进展,为临床治疗提供指导。