Lv Xiaoman, Zhao Ting, Dai Youwu, Shi Mingqin, Huang Xiaoyi, Wei Yuanyuan, Shen Jiayan, Zhang Xiaoyu, Xie Zhaohu, Wang Qi, Li Zhaofu, Qin Dongdong
School of Basic Medical Sciences, Yunnan University of Chinese Medicine, Kunming, China.
The First School of Clinical Medicine, Yunnan University of Chinese Medicine, Kunming, China.
Front Cell Dev Biol. 2022 Dec 5;10:1089668. doi: 10.3389/fcell.2022.1089668. eCollection 2022.
Autophagy is an intracellular degradation system that maintains the stable state of cell energy metabolism. Some recent findings have indicated that autophagy dysfunction is an important driving factor for the occurrence and development of osteoarthritis (OA). The decrease of autophagy leads to the accumulation of damaged organelles and macromolecules in chondrocytes, which affects the survival of chondrocytes and ultimately leads to OA. An appropriate level of autophagic activation may be a new method to prevent articular cartilage degeneration in OA. This minireview discussed the mechanism of autophagy and OA, key autophagy targets regulating OA progression, and evaluated therapeutic applications of drugs targeting autophagy in preclinical and clinical research. Some critical issues worth paying attention to were also raised to guide future research efforts.
自噬是一种维持细胞能量代谢稳定状态的细胞内降解系统。最近的一些研究结果表明,自噬功能障碍是骨关节炎(OA)发生发展的重要驱动因素。自噬的减少导致软骨细胞中受损细胞器和大分子的积累,这影响软骨细胞的存活并最终导致OA。适当水平的自噬激活可能是预防OA中关节软骨退变的一种新方法。这篇综述讨论了自噬与OA的机制、调节OA进展的关键自噬靶点,并评估了靶向自噬的药物在临床前和临床研究中的治疗应用。还提出了一些值得关注的关键问题,以指导未来的研究工作。