The osteoarthritic niche and modulation of skeletal stem cell function for regenerative medicine

被引:3
|
作者
Williams, E. L. [1 ,2 ]
Edwards, C. J. [1 ,2 ]
Cooper, C. [2 ,3 ]
Oreffo, R. O. C. [1 ]
机构
[1] Univ Southampton, Bone & Joint Res Grp, Sch Med, Southampton SO9 5NH, Hants, England
[2] Univ Hosp Southampton NHS Fdn Trust, Dept Rheumatol, Southampton SO16 6YD, Hants, England
[3] Univ Hosp Southampton NHS Fdn Trust, MRC Lifecourse Epidemiol Unit, Southampton SO16 6YD, Hants, England
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会; 英国医学研究理事会;
关键词
osteoarthritis; mesenchymal stem cell; tissue engineering; epigenetics; skeletal stem cell; TUMOR-NECROSIS-FACTOR; HUMAN ARTICULAR CHONDROCYTES; SUBCHONDRAL BONE OSTEOBLASTS; TISSUE-ENGINEERED BONE; NF-KAPPA-B; SYNOVIAL LINING MACROPHAGES; CYCLIC MECHANICAL STRAIN; MARROW STROMAL CELLS; GROWTH-FACTOR-BETA; FACTOR-ALPHA;
D O I
10.1002/term.1455
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Osteoarthritis (OA) is the most common cause of arthritis worldwide and represents a significant healthcare burden, particularly in the context of an ageing population. Traditionally, painkillers, injections and physiotherapy have been the mainstay of treatment, with patients being referred for joint replacement surgery (arthroplasty) when these options fail. Whilst effective in reducing pain and improving joint function, these approaches are not without potential complications. With the development of tissue-engineering techniques over recent years there has been considerable interest in applying these strategies to provide new, innovative, alternative effective means of treating OA. This review explores the unique microenvironment present within an osteoarthritic joint, highlighting the features that comprise the osteoarthritic niche and could be modulated in the development of novel treatments for OA. Existing tissue-engineering strategies for repairing bone and cartilage defects are discussed, with particular reference to how these might be modified, both to improve existing treatments, such as impaction bone grafting, as well as in the development of future treatments for OA. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:589 / 608
页数:20
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