Wang Dong, He Xin, Zheng Chao, Wang Chengzhe, Peng Pandi, Gao Chu, Xu Xiaolong, Ma Yachao, Liu Mei, Yang Liu, Luo Zhuojing
Institute of Orthopedic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Pharmacy Department, Air Force Hospital of Eastern Theater Command, Nanjing, China.
Front Cell Dev Biol. 2022 Feb 1;9:819139. doi: 10.3389/fcell.2021.819139. eCollection 2021.
Low back pain (LBP) is a global health issue. Intervertebral disc degeneration (IDD) is a major cause of LBP. Although the explicit mechanisms underpinning IDD are unclear, endoplasmic reticulum (ER) stress caused by aberrant unfolded or misfolded proteins may be involved. The accumulation of unfolded/misfolded proteins may result in reduced protein synthesis and promote aberrant protein degradation to recover ER function, a response termed the unfolded protein response. A growing body of literature has demonstrated the potential relationships between ER stress and the pathogenesis of IDD, indicating some promising therapeutic targets. In this review, we summarize the current knowledge regarding the impact of ER stress on the process of IDD, as well as some potential therapeutic strategies for alleviating disc degeneration by targeting different pathways to inhibit ER stress. This review will facilitate understanding the pathogenesis and progress of IDD and highlights potential therapeutic targets for treating this condition.
下腰痛(LBP)是一个全球性的健康问题。椎间盘退变(IDD)是LBP的主要原因。尽管IDD背后的确切机制尚不清楚,但由异常未折叠或错误折叠的蛋白质引起的内质网(ER)应激可能与之有关。未折叠/错误折叠蛋白质的积累可能导致蛋白质合成减少,并促进异常蛋白质降解以恢复内质网功能,这种反应称为未折叠蛋白反应。越来越多的文献表明内质网应激与IDD发病机制之间存在潜在关系,这表明了一些有前景的治疗靶点。在本综述中,我们总结了关于内质网应激对IDD过程影响的当前知识,以及一些通过靶向不同途径抑制内质网应激来减轻椎间盘退变的潜在治疗策略。本综述将有助于理解IDD的发病机制和进展,并突出治疗该疾病的潜在治疗靶点。