Controlled treadmill exercise eliminates chondroid deposits and restores tensile properties in a new murine tendinopathy model

被引:48
作者
Bell, Rebecca [1 ]
Li, Jun [2 ]
Gorski, Daniel J. [3 ]
Bartels, Anne K. [1 ]
Shewman, Elizabeth F. [1 ]
Wysocki, Robert W. [1 ]
Cole, Brian J. [1 ]
Bach, Bernard R., Jr. [1 ]
Mikecz, Katalin [1 ]
Sandy, John D. [3 ]
Plaas, Anna H. [2 ]
Wang, Vincent M. [1 ]
机构
[1] Rush Univ, Med Ctr, Dept Orthoped Surg, Chicago, IL 60612 USA
[2] Rush Univ, Med Ctr, Dept Rheumatol Internal Med, Chicago, IL 60612 USA
[3] Rush Univ, Med Ctr, Dept Biochem, Chicago, IL 60612 USA
关键词
Tendinopathy; Collagen; Aggrecan; Gene expression; Mechanical loading; 5-YEAR FOLLOW-UP; ACHILLES TENDINOPATHY; PATELLAR TENDINOPATHY; AGGRECAN ACCUMULATION; MESSENGER-RNA; JUMPERS KNEE; TENDON; ADAMTS5; DIFFERENTIATION; OSTEOARTHRITIS;
D O I
10.1016/j.jbiomech.2012.10.020
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Tendinopathy is a widespread and disabling condition characterized by collagen fiber disruption and accumulation of a glycosaminoglycan-rich chondroid matrix. Recent clinical reports have illustrated the potential of mechanical loading (exercise) therapies to successfully treat chronic tendinopathies. We have developed a new murine tendinopathy model which requires a single injection of TGF-beta 1 into the Achilles tendon midsubstance followed by normal cage activity for 2 weeks. At this time, tendon maximum stress showed a dramatic (66%) reduction relative to that of normal controls and this persisted at four weeks. Loss of material properties was accompanied by abundant chondroid cells within the tendon (closely resembling the changes observed in human samples obtained intra-operatively) and increased expression of Acan, Col1a1, Col2a1, Col3a1, Fn1 and Mmp3. Mice subjected to two weeks of daily treadmill exercise following TGF-beta 1 injection showed a similar reduction in tendon material properties as the caged group. However, in mice subjected to 4 weeks of treadmill exercise, tendon maximum stress values were similar to those of naive controls. Tendons from the mice exercised for 4 weeks showed essentially no chondroid cells and the expression of Acan, Col1a1, Col2a1, Col3a1, and Mmp3 was significantly reduced relative to the 4-week cage group. This technically simple murine tendinopathy model is highly amenable to detailed mechanistic and translational studies of the biomechanical and cell biological pathways, that could be targeted to enhance healing of tendinopathy. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:498 / 505
页数:8
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