Department of Joint Surgery, the Affiliated Hospital of Qingdao University, Qingdao, 266000, Shandong Province, China.
Arthritis Res Ther. 2022 Jul 22;24(1):174. doi: 10.1186/s13075-022-02859-x.
Osteoarthritis (OA) is an age-related cartilage degenerative disease, and chondrocyte senescence has been extensively studied in recent years. Increased numbers of senescent chondrocytes are found in OA cartilage. Selective clearance of senescent chondrocytes in a post-traumatic osteoarthritis (PTOA) mouse model ameliorated OA development, while intraarticular injection of senescent cells induced mouse OA. However, the means and extent to which senescence affects OA remain unclear. Here, we review the latent mechanism of senescence in OA and propose potential therapeutic methods to target OA-related senescence, with an emphasis on immunotherapies. Natural killer (NK) cells participate in the elimination of senescent cells in multiple organs. A relatively comprehensive discussion is presented in that section. Risk factors for OA are ageing, obesity, metabolic disorders and mechanical overload. Determining the relationship between known risk factors and senescence will help elucidate OA pathogenesis and identify optimal treatments.
骨关节炎(OA)是一种与年龄相关的软骨退行性疾病,近年来人们对软骨细胞衰老进行了广泛研究。OA 软骨中发现衰老软骨细胞数量增加。在创伤后骨关节炎(PTOA)小鼠模型中,选择性清除衰老软骨细胞可改善 OA 发生,而关节内注射衰老细胞可诱导小鼠 OA。然而,衰老对 OA 的影响方式和程度尚不清楚。本文综述了 OA 中衰老的潜在机制,并提出了针对 OA 相关衰老的潜在治疗方法,重点是免疫疗法。自然杀伤(NK)细胞参与多个器官中衰老细胞的清除。该部分进行了相对全面的讨论。OA 的危险因素包括年龄、肥胖、代谢紊乱和机械过载。确定已知危险因素与衰老之间的关系将有助于阐明 OA 的发病机制并确定最佳治疗方法。