Role of crosstalk between synovial cells and chondrocytes in osteoarthritis (Review)

被引:6
|
作者
Chen, Baisen [1 ,2 ]
Sun, Yuyu [3 ]
Xu, Guanhua [1 ,2 ]
Jiang, Jiawei [1 ,2 ]
Zhang, Wenhao [4 ]
Wu, Chunshuai [1 ,2 ]
Xue, Pengfei [1 ,2 ]
Cui, Zhiming [1 ,2 ]
机构
[1] Nantong Univ, Nantong City 1 Peoples Hosp, Dept Orthoped, 666 Shengli Rd, Nantong 226001, Jiangsu, Peoples R China
[2] Nantong Univ, Affiliated Hosp 2, 666 Shengli Rd, Nantong 226001, Jiangsu, Peoples R China
[3] Nantong Third Peoples Hosp, Dept Orthoped, Nantong 226003, Jiangsu, Peoples R China
[4] Nantong Univ, Med Sch, Nantong 226001, Jiangsu, Peoples R China
关键词
cellular interaction; OA; exosomes; chondrocytes; synovial cells; MESENCHYMAL STEM-CELLS; PATTERN-RECOGNITION RECEPTORS; KNEE OSTEOARTHRITIS; ARTICULAR-CARTILAGE; SUBCHONDRAL BONE; STROMAL CELLS; INFLAMMATION; PROGRESSION; MACROPHAGES; PATHOGENESIS;
D O I
10.3892/etm.2024.12490
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Osteoarthritis (OA) is a low-grade, nonspecific inflammatory disease that affects the entire joint. This condition is characterized by synovitis, cartilage erosion, subchondral bone defects, and subpatellar fat pad damage. There is mounting evidence demonstrating the significance of crosstalk between synovitis and cartilage destruction in the development of OA. To comprehensively explore the phenotypic alterations of synovitis and cartilage destruction, it is important to elucidate the crosstalk mechanisms between chondrocytes and synovial cells. Furthermore, the updated iteration of single-cell sequencing technology reveals the interaction between chondrocyte and synovial cells. In the present review, the histological and pathological alterations between cartilage and synovium during OA progression are described, and the mode of interaction and molecular mechanisms between synovial cells and chondrocytes in OA, both of which affect the OA process mainly by altering the inflammatory environment and cellular state, are elucidated. Finally, the current OA therapeutic approaches are summarized and emerging therapeutic targets are reviewed in an attempt to provide potential insights into OA treatment.
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收藏
页数:16
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