Muscle-bone interactions during fracture healing

被引:2
|
作者
Davis, K. M. [1 ]
Griffin, K. S. [1 ]
Chu, T-M. G. [2 ]
Wenke, J. C. [3 ]
Corona, B. T. [3 ]
McKinley, T. O. [1 ]
Kacena, M. A. [1 ]
机构
[1] Indiana Univ Sch Med, Dept Orthopaed Surg, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Dept Restorat Dent, Indianapolis, IN 46202 USA
[3] United States Army Inst Surg Res, Extrem Trauma & Regenerat Med Task Area, San Antonio, TX USA
关键词
Muscle; Bone; Fracture; Mesenchymal Stem Cells; Paracrine; MESENCHYMAL STEM-CELLS; HUMAN SKELETAL-MUSCLE; MYOSTATIN-DEFICIENT MICE; GROWTH-FACTOR GENE; FACTOR-I IGF-1; SATELLITE CELLS; FLAP COVERAGE; OSTEOBLASTIC DIFFERENTIATION; OSTEOGENIC DIFFERENTIATION; MORPHOGENETIC PROTEIN-2;
D O I
暂无
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although it is generally accepted that the rate and strength of fracture healing is intimately linked to the integrity of surrounding soft tissues, the contribution of muscle has largely been viewed as a vascular supply for oxygen and nutrient exchange. However, more is becoming known about the cellular and paracrine contributions of muscle to the fracture healing process. Research has shown that muscle is capable of supplying osteoprogenitor cells in cases where the periosteum is insufficient, and the muscular osteoprogenitors possess similar osteogenic potential to those derived from the periosteum. Muscle's secrotome includes proteins capable of inhibiting or enhancing osteogenesis and myogenesis following musculoskeletal injury and can be garnered for therapeutic use in patients with traumatic musculoskeletal injuries. In this review, we will highlight the current knowledge on muscle-bone interaction in the context of fracture healing as well as concisely present the current models to study such interactions.
引用
收藏
页码:1 / 9
页数:9
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