Mechanical Signaling for Bone Modeling and Remodeling

被引:250
|
作者
Robling, Alexander G. [1 ,2 ]
Turner, Charles H. [1 ,3 ]
机构
[1] Indiana Univ Purdue Univ, Dept Biomed Engn, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Anat & Cell Biol, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Orthopaed Surg, Indianapolis, IN 46202 USA
来源
基金
美国国家卫生研究院;
关键词
mechanical loading; bone mechanotransduction; bone strength; adaptation; osteoblasts; osteocytes; Wnt signaling; focal adhesion; bone turnover; bone modeling; nitric oxide; prostaglandin; desensitization; NITRIC-OXIDE SYNTHASE; FLUID SHEAR-STRESS; ESTROGEN-RECEPTOR-ALPHA; LOADING IN-VIVO; STROMAL CELLS; OSTEOCYTE APOPTOSIS; CORTICAL BONE; RAT ULNA; SKELETAL MECHANOTRANSDUCTION; RANKL EXPRESSION;
D O I
10.1615/CritRevEukarGeneExpr.v19.i4.50
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Proper development of the skeleton in utero and during growth requires mechanical stimulation. Loading results in adaptive changes in bone that strengthen bone structure. Bone's adaptive response is regulated by the ability of resident bone cells to perceive and translate mechanical energy into a cascade of structural and biochemical changes within the cells - a process known as mechanotransduction. Mechanotransduction pathways are among the most anabolic in bone, and consequently, there is great interest in elucidating how mechanical loading produces its observed effects, including increased bone formation, reduced bone loss, changes in bone cell differentiation and lifespan, among others. A molecular understanding of these processes is developing, and with it comes a profound new insight into the biology of bone. In this article, we review the nature of the physical stimulus to which bone cells mount an adaptive response, including the identity of the sensor cells, their attributes and physical environment, and putative mechanoreceptors they express. Particular attention is allotted to the focal adhesion and Wnt signaling, in light of their emerging role in bone mechanotransduction. The cellular mechanisms for increased bone loss during disuse, and reduced bone loss during loading a-re considered. Finally, we summarize the published data on bone cell accommodation, whereby bone cells stop responding to mechanical signaling events. Collectively, these data highlight the complex yet finely orchestrated process of mechanically regulated bone homeostasis.
引用
收藏
页码:319 / 338
页数:20
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