Li Shangze, Jiang Wenli, Chen Fei, Qian Jiao, Yang Jun
Department of Orthopedics, The Second Affiliated Hospital (Shanghai Changzheng Hospital), Naval Medical University, Shanghai, China.
Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Naval Medical University, Shanghai, China.
Front Cell Dev Biol. 2025 Feb 6;13:1525073. doi: 10.3389/fcell.2025.1525073. eCollection 2025.
Intervertebral disc degeneration (IVDD) is a leading cause of chronic back pain, contributing significantly to reduced quality of life and global public health burdens. The TRIM (Tripartite Motif-containing) protein family, with its diverse regulatory roles, has emerged as a key player in critical cellular processes such as inflammation, cell death, and extracellular matrix (ECM) metabolism. Recent findings underscore the involvement of TRIM proteins in IVDD pathogenesis, where they regulate stress responses, maintain cellular homeostasis, and influence the functional integrity of nucleus pulposus (NP) and annulus fibrosus (AF) cells. This review explores the multifaceted roles of TRIM proteins in IVDD, highlighting their contributions to pathological pathways and their potential as therapeutic targets. Advancing our understanding of TRIM protein-mediated mechanisms may pave the way for innovative and precise therapeutic strategies to combat IVDD.
椎间盘退变(IVDD)是慢性背痛的主要原因,对生活质量下降和全球公共卫生负担有重大影响。TRIM(含三重基序)蛋白家族具有多种调节作用,已成为炎症、细胞死亡和细胞外基质(ECM)代谢等关键细胞过程中的关键参与者。最近的研究结果强调了TRIM蛋白在IVDD发病机制中的作用,它们在其中调节应激反应、维持细胞稳态,并影响髓核(NP)和纤维环(AF)细胞的功能完整性。本综述探讨了TRIM蛋白在IVDD中的多方面作用,强调了它们对病理途径的贡献及其作为治疗靶点的潜力。加深我们对TRIM蛋白介导机制的理解可能为对抗IVDD的创新和精确治疗策略铺平道路。