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

被引:228
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
100224 [整形外科学];
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
相关论文
共 125 条
[81]
Oral salmon calcitonin reduces cartilage and bone pathology in an osteoarthritis rat model with increased subchondral bone turnover [J].
Nielsen, R. H. ;
Bay-Jensen, A. -C. ;
Byrjalsen, I. ;
Karsdal, M. A. .
OSTEOARTHRITIS AND CARTILAGE, 2011, 19 (04) :466-473
[82]
Alendronate treatment for hip osteoarthritis: prospective randomized 2-year trial [J].
Nishii, Takashi ;
Tamura, Satoru ;
Shiomi, Toshiyuki ;
Yoshikawa, Hideki ;
Sugano, Nobuhiko .
CLINICAL RHEUMATOLOGY, 2013, 32 (12) :1759-1766
[83]
PTH [1-34]-induced alterations of the subchondral bone provoke early osteoarthritis [J].
Orth, P. ;
Cucchiarini, M. ;
Wagenpfeil, S. ;
Menger, M. D. ;
Madry, H. .
OSTEOARTHRITIS AND CARTILAGE, 2014, 22 (06) :813-821
[84]
Elevated cross-talk between subchondral bone and cartilage in osteoarthritic joints [J].
Pan, Jun ;
Wang, Bin ;
Li, Wen ;
Zhou, Xiaozhou ;
Scherr, Thomas ;
Yang, Yunyi ;
Price, Christopher ;
Wang, Liyun .
BONE, 2012, 51 (02) :212-217
[85]
In Situ Measurement of Transport between Subchondral Bone and Articular Cartilage [J].
Pan, Jun ;
Zhou, Xiaozhou ;
Li, Wen ;
Novotny, John E. ;
Doty, Stephen B. ;
Wang, Liyun .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2009, 27 (10) :1347-1352
[86]
Strontium ranelate reduces the progression of experimental dog osteoarthritis by inhibiting the expression of key proteases in cartilage and of IL-1β in the synovium [J].
Pelletier, Jean-Pierre ;
Kapoor, Mohit ;
Fahmi, Hassan ;
Lajeunesse, Daniel ;
Blesius, Alexia ;
Maillet, Juliette ;
Martel-Pelletier, Johanne .
ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 (02) :250-257
[87]
Hepatocyte growth factor in human osteoarthritic cartilage [J].
Pfander, D ;
Cramer, T ;
Weseloh, G ;
Pullig, O ;
Schuppan, D ;
Bauer, M ;
Swoboda, B .
OSTEOARTHRITIS AND CARTILAGE, 1999, 7 (06) :548-559
[88]
Impact of extracellular matrix derived from osteoarthritis subchondral bone osteoblasts on osteocytes: role of integrinβ1 and focal adhesion kinase signaling cues [J].
Prasadam, Indira ;
Farnaghi, Saba ;
Feng, Jian Q. ;
Gu, Wenyi ;
Perry, Samuel ;
Crawford, Ross ;
Xiao, Yin .
ARTHRITIS RESEARCH & THERAPY, 2013, 15 (05)
[89]
New findings in osteoarthritis pathogenesis: therapeutic implications [J].
Pulsatelli, Lia ;
Addimanda, Olga ;
Brusi, Veronica ;
Pavloska, Branka ;
Meliconi, Riccardo .
THERAPEUTIC ADVANCES IN CHRONIC DISEASE, 2013, 4 (01) :23-43
[90]
Maintenance of antifracture efficacy over 10 years with strontium ranelate in postmenopausal osteoporosis [J].
Reginster, J-Y. ;
Kaufman, J-M. ;
Goemaere, S. ;
Devogelaer, J. P. ;
Benhamou, C. L. ;
Felsenberg, D. ;
Diaz-Curiel, M. ;
Brandi, M-L. ;
Badurski, J. ;
Wark, J. ;
Balogh, A. ;
Bruyere, O. ;
Roux, C. .
OSTEOPOROSIS INTERNATIONAL, 2012, 23 (03) :1115-1122