Gao Tianyang, Guo Weimin, Chen Mingxue, Huang Jingxiang, Yuan Zhiguo, Zhang Yu, Wang Mingjie, Li Penghao, Peng Jiang, Wang Aiyuan, Wang Yu, Sui Xiang, Zhang Li, Xu Wenjing, Lu Shibi, Zhang Xifeng, Liu Shuyun, Guo Quanyi
Institute of Orthopaedics, Chinese PLA General Hospital, Beijing Key Lab of Regenerative Medicine in Orthopaedics, Key Laboratory of Musculoskeletal Trauma & War Injuries, 28 Fuxing Road, Haidian District, Beijing 100853, China; Shanxi Medical University, No. 56 XinJiannan Road, YingZe District, Taiyuan 030001, China.
Institute of Orthopaedics, Chinese PLA General Hospital, Beijing Key Lab of Regenerative Medicine in Orthopaedics, Key Laboratory of Musculoskeletal Trauma & War Injuries, 28 Fuxing Road, Haidian District, Beijing 100853, China.
Biomed Res Int. 2016;2016:2428915. doi: 10.1155/2016/2428915. Epub 2016 Dec 18.
Osteoarthritis (OA) is a type of chronic joint disease that is characterized by the degeneration and loss of articular cartilage and hyperplasia of the synovium and subchondral bone. There is reasonable knowledge about articular cartilage physiology, biochemistry, and chondrocyte metabolism. However, the etiology and pathogenesis of OA remain unclear and need urgent clarification to guide the early diagnosis and treatment of OA. Extracellular vesicles (EVs) are small membrane-linking particles that are released from cells. In recent decades, several special biological properties have been found in EV, especially in terms of cartilage. Autophagy plays a critical role in the regulation of cellular homeostasis. Likewise, more and more research has gradually focused on the effect of autophagy on chondrocyte proliferation and function in OA. The synthesis and release of EV are closely associated with autophagy. At the same time, both EV and autophagy play a role in OA development. Based on the mechanism of EV and autophagy in OA development, EV may be beneficial in the early diagnosis of OA; on the other hand, the combination of EV and autophagy-related regulatory drugs may provide insight into possible OA therapeutic strategies.
骨关节炎(OA)是一种慢性关节疾病,其特征在于关节软骨的退化和丧失以及滑膜和软骨下骨的增生。人们对关节软骨的生理学、生物化学和软骨细胞代谢有一定的了解。然而,OA的病因和发病机制仍不清楚,需要迫切阐明以指导OA的早期诊断和治疗。细胞外囊泡(EVs)是从细胞中释放出来的小的膜连接颗粒。近几十年来,在EV中发现了一些特殊的生物学特性,尤其是在软骨方面。自噬在细胞内稳态的调节中起关键作用。同样,越来越多的研究逐渐聚焦于自噬对OA中软骨细胞增殖和功能的影响。EV的合成和释放与自噬密切相关。同时,EV和自噬都在OA的发展中起作用。基于EV和自噬在OA发展中的机制,EV可能有助于OA的早期诊断;另一方面,EV与自噬相关调节药物的联合应用可能为OA的潜在治疗策略提供思路。