Exploration of the mode of death and potential death mechanisms of nucleus pulposus cells

上睑下垂 程序性细胞死亡 坏死性下垂 变性(医学) 衰老 生物 椎间盘 细胞凋亡 死因 炎症 细胞生物学 生物信息学 神经科学 医学 疾病 病理 免疫学 遗传学 解剖
作者
Daqian Zhou,Yongliang Mei,Chao Song,Kang Cheng,Weiye Cai,Daru Guo,Silong Gao,Jiale Lv,Tao Liu,Yang Zhou,Liquan Wang,Bing Liu,Zongchao Liu
出处
期刊:European Journal of Clinical Investigation [Wiley]
卷期号:54 (9): e14226-e14226 被引量:31
标识
DOI:10.1111/eci.14226
摘要

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.
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