Extracellular Vesicles and Autophagy in Osteoarthritis

Author:

Gao Tianyang12ORCID,Guo Weimin1,Chen Mingxue1,Huang Jingxiang1,Yuan Zhiguo1,Zhang Yu1,Wang Mingjie1,Li Penghao1,Peng Jiang1ORCID,Wang Aiyuan1,Wang Yu1,Sui Xiang1,Zhang Li1,Xu Wenjing1,Lu Shibi1,Zhang Xifeng3ORCID,Liu Shuyun1ORCID,Guo Quanyi1ORCID

Affiliation:

1. 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

2. Shanxi Medical University, No. 56 XinJiannan Road, YingZe District, Taiyuan 030001, China

3. Minimal Invasive Spine Surgery Center, Spine Division of Orthopaedic Department, Chinese PLA General Hospital, 28 Fuxing Road, Haidian District, Beijing 100853, China

Abstract

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.

Funder

National High Technology Research and Development Program of China

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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