Chondrocyte hypertrophy and osteoarthritis: role in initiation and progression of cartilage degeneration?

被引:539
作者
van der Kraan, P. M. [1 ]
van den Berg, W. B. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Rheumatol, NL-6525 Nijmegen, Netherlands
关键词
Chondrocyte; Hypertrophy; Terminal differentiation; Calcification; Transcription factors; HUMAN ARTICULAR-CARTILAGE; GROWTH-FACTOR-BETA; DOMAIN RECEPTOR 2; KNEE-JOINT INSTABILITY; MESENCHYMAL STEM-CELLS; AGE-RELATED-CHANGES; GENE-EXPRESSION; TGF-BETA; ENDOCHONDRAL OSSIFICATION; TERMINAL DIFFERENTIATION;
D O I
10.1016/j.joca.2011.12.003
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
Objective: To review the literature on the role and regulation of chondrocyte terminal differentiation (hypertrophy-like changes) in osteoarthritis (OA) and to integrate this in a conceptual model of primary OA development. Methods: Papers investigating chondrocyte terminal differentiation in human OA cartilage and experimental models of OA were recapitulated and discussed. Focus has been on the occurrence of hypertrophy-like changes in chondrocytes and the factors described to play a role in regulation of chondrocyte hypertrophy-like changes in OA. Results: Chondrocyte hypertrophy-like changes are reported in both human OA and experimental OA models by most investigators. These changes play a crucial part in the OA disease process by protease-mediated cartilage degradation. We propose that altered chondrocyte behavior and concomitant cartilage degradation result in a disease-amplifying loop, leading to a mixture of disease stages and cellular responses within an OA joint. Conclusion: Chondrocyte hypertrophy-like changes play a role in early and late stage OA. Since not all cells in an OA joint are synchronized, inhibition of hypertrophy-like changes might be a therapeutic target to slow down further OA progression. (C) 2011 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:223 / 232
页数:10
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