The Clinical Medical College, Guizhou Medical University, Guiyang 550004, China.
The First Clinical Medical College, Lanzhou University, Lanzhou 730000, China.
Biomolecules. 2022 Dec 2;12(12):1804. doi: 10.3390/biom12121804.
Intervertebral disc degeneration (IDD), a progressive and multifactorial pathological process, is predominantly associated with low back pain and permanent disability. Pyroptosis is a type of lytic programmed cell death triggered by the activation of inflammasomes and caspases. Unlike apoptosis, pyroptosis is characterized by the rupture of the plasma membrane and the release of inflammatory mediators, accelerating the destruction of the extracellular matrix (ECM). Recent studies have shown that pyrin domain-containing 3 (NLRP3) inflammasome-mediated pyroptosis in nucleus pulposus (NP) cells is activated in the progression of IDD. Furthermore, targeting pyroptosis in IDD demonstrates the excellent capacity of ECM remodeling and its anti-inflammatory properties, suggesting that pyroptosis is involved in the IDD process. In this review, we briefly summarize the molecular mechanism of pyroptosis and the pathogenesis of IDD. We also focus on the role of pyroptosis in the pathological progress of IDD and its targeted therapeutic application.
椎间盘退变性疾病(IDD)是一种进行性的、多因素的病理过程,主要与下腰痛和永久性残疾有关。细胞焦亡是一种由炎性小体和半胱天冬酶激活引发的、有别于细胞凋亡的、溶酶体依赖性的程序性细胞死亡方式。细胞焦亡的特点是细胞膜破裂和炎症介质的释放,从而加速细胞外基质(ECM)的破坏。最近的研究表明,核髓核细胞中吡咯烷二硫代氨基甲酸盐(pyrin)域包含 3(NLRP3)炎性小体介导的细胞焦亡在 IDD 的进展中被激活。此外,针对 IDD 中的细胞焦亡显示出 ECM 重塑的出色能力及其抗炎特性,表明细胞焦亡参与了 IDD 过程。在这篇综述中,我们简要总结了细胞焦亡的分子机制和 IDD 的发病机制。我们还重点关注了细胞焦亡在 IDD 病理进展中的作用及其靶向治疗应用。