Advances in Regenerative Orthopedics

被引:68
作者
Evans, Christopher H. [1 ,2 ]
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Ctr Adv Orthopaed Studies, Sch Med, Boston, MA 02215 USA
[2] AO Fdn, Collaborat Res Ctr, Davos, Switzerland
基金
美国国家卫生研究院;
关键词
MESENCHYMAL STEM-CELLS; ARTICULAR-CARTILAGE DEFECTS; RAAV-MEDIATED OVEREXPRESSION; REGIONAL GENE-THERAPY; IN-VIVO; PROGENITOR CELLS; TRANSFORMING GROWTH-FACTOR-BETA-1; EXTRACELLULAR-MATRIX; BONE REGENERATION; ANIMAL-MODELS;
D O I
10.1016/j.mayocp.2013.04.027
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Orthopedic injuries are common and a source of much misery and economic stress. Several relevant tissues, such as cartilage, meniscus, and intra-articular ligaments, do not heal. And even bone, which normally regenerates spontaneously, can fail to mend. The regeneration of orthopedic tissues requires 4 key components: cells, morphogenetic signals, scaffolds, and an appropriate mechanical environment. Although differentiated cells from the tissue in question can be used, most cellular research focuses on the use of mesenchymal stem cells. These can be retrieved from many different tissues, and one unresolved question is the degree to which the origin of the cells matters. Embryonic and induced pluripotent stem cells are also under investigation. Morphogenetic signals are most frequently supplied by individual recombinant growth factors or native mixtures provided by, for example, platelet-rich plasma; mesenchymal stem cells are also a rich source of trophic factors. Obstacles to the sustained delivery of individual growth factors can be addressed by gene transfer or smart scaffolds, but we still lack detailed, necessary information on which delivery profiles are needed. Scaffolds may be based on natural products, synthetic materials, or devitalized extracellular matrix. Strategies to combine these components to regenerate tissue can follow traditional tissue engineering practices, but these are costly, cumbersome, and not well suited to treating large numbers of individuals. More expeditious approaches make full use of intrinsic biological processes in vivo to avoid the need for ex vivo expansion of autologous cells and multiple procedures. Clinical translation remains a bottleneck. (C) 2013 Mayo Foundation for Medical Education and Research
引用
收藏
页码:1323 / 1339
页数:17
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