Bone-cartilage interface crosstalk in osteoarthritis: potential pathways and future therapeutic strategies

被引:222
|
作者
Yuan, X. L. [1 ]
Meng, H. Y. [1 ]
Wang, Y. C. [1 ]
Peng, J. [1 ]
Guo, Q. Y. [1 ]
Wang, A. Y. [1 ]
Lu, S. B. [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Inst Orthoped, Beijing, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
Osteoarthritis; Bone-cartilage interface; Subchondral bone; Crosstalk; Molecular interaction; HEPATOCYTE GROWTH-FACTOR; HYPOXIA-INDUCIBLE FACTOR-2-ALPHA; MESENCHYMAL STEM-CELLS; SUBCHONDRAL BONE; ARTICULAR-CARTILAGE; KNEE OSTEOARTHRITIS; STRONTIUM RANELATE; RAT MODEL; PARATHYROID-HORMONE; HIP OSTEOARTHRITIS;
D O I
10.1016/j.joca.2014.05.023
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Currently, osteoarthritis (OA) is considered a disease of the entire joint, which is not simply a process of wear and tear but rather abnormal remodelling and joint failure of an organ. The bone-cartilage interface is therefore a functioning synergistic unit, with a close physical association between subchondral bone and cartilage suggesting the existence of biochemical and molecular crosstalk across the OA interface. The crosstalk at the bone-cartilage interface may be elevated in OA in vivo and in vitro. Increased vascularisation and formation of microcracks associated with abnormal bone remodelling in joints during OA facilitate molecular transport from cartilage to bone and vice versa. Recent reports suggest that several critical signalling pathways and biological factors are key regulators and activate cellular and molecular processes in crosstalk among joint compartments. Therapeutic interventions including angiogenesis inhibitors, agonists/antagonists of molecules and drugs targeting bone remodelling are potential candidates for this interaction. This review summarised the premise for the presence of crosstalk in bone-cartilage interface as well as the current knowledge of the major signalling pathways and molecular interactions that regulate OA progression. A better understanding of crosstalk in bone-cartilage interface may lead to development of more effective strategies for treating OA patients. (C) 2014 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1077 / 1089
页数:13
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