The effect of dynamic compression on the response of articular cartilage to insulin-like growth factor-I

被引:184
作者
Bonassar, LJ
Grodzinsky, AJ
Frank, EH
Davila, SG
Bhaktav, NR
Trippel, SB [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Orthopaed Res Labs, Boston, MA 02114 USA
[2] MIT, Dept Elect Engn & Comp Sci, Ctr Biomed Engn, Cambridge, MA 02139 USA
关键词
D O I
10.1016/S0736-0266(00)00004-8
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
Articular cartilage is routinely subjected to mechanical farces and to cell-regulatory molecules, Previous studies have shown that mechanical stimuli can influence articular chondrocyte metabolic activity, and biochemical studies have shown that growth factors and cytokines control many of the same cell functions. Little is known, however, of the relationships or interplay, if any, between these two key components of the articular environment. This study investigated the comparative and interactive effects of low amplitude, sinusoidal. dynamic compression: and insulin-like growth factor-I (IGF-I) a polypeptide in synovial fluid that is anabolic for cartilage. In bovine patellofemoral cartilage explants, IGF-I increased protein and proteoglycan synthesis 90%, and 120%. respectively while dynamic compression increased protein and proteoglycan synthesis 40% and 90%, respectively. Stimulation by IC;FI was significantly greater than by dynamic compression for both protein and proteoglycan synthesis. When applied together, the two stimuli enhanced protein and proteoglycan synthesis by 180% and 290%, respectively, a degree greater than that achieved by either stimulus alone. IGF-I augmented protein synthesis with a time constant of 12.2 h. Dynamic compression increased protein synthesis with a time constant of 2.9 h, a rate significantly faster than that of IGF-I, suggesting that these signals act via distinct cell activation pathways. When used together, dynamic compression and IGF-I acted with a time constant of 5.6 h. Thus, dynamic compression accelerated the biosynthetic response to IGF-I and increased transport of IGF-I into the articular cartilage matrix, suggesting that, in addition to independently stimulating articular chondrocytes, cyclic compression may improve the access of soluble growth factors to these relatively isolated cells. (C) 2001 Orthopaedic Research Society. Published by Elsevier Science Ltd. All rights reserved.
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页码:11 / 17
页数:7
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