The relationships among spatiotemporal collagen gene expression, histology, and biomechanics following full-length injury in the murine patellar tendon

被引:43
作者
Dyment, Nathaniel A. [1 ]
Kazemi, Namdar [2 ]
Aschbacher-Smith, Lindsey E. [3 ]
Barthelery, Nicolas J. [3 ]
Kenter, Keith [2 ]
Gooch, Cynthia [1 ]
Shearn, Jason T. [1 ]
Wylie, Christopher [3 ]
Butler, David L. [1 ]
机构
[1] Univ Cincinnati, Sch Energy Environm Biol & Med Engn, Biomed Engn Program, Cincinnati, OH 45221 USA
[2] Univ Cincinnati, Coll Med, Dept Orthopaed Surg, Cincinnati, OH USA
[3] Cincinnati Childrens Hosp Res Fdn, Div Dev Biol, Cincinnati, OH USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
tendon; collagen; murine; transgenic; healing; MECHANICAL STIMULATION; SPONGE CONSTRUCTS; BONE INSERTION; REPAIR; FORCES;
D O I
10.1002/jor.21484
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
100224 [整形外科学];
摘要
Tendon injuries are major orthopedic problems that worsen as the population ages. Type-I (Col1) and type-II (Col2) collagens play important roles in tendon midsubstance and tendon-to-bone insertion healing, respectively. Using double transgenic mice, this study aims to spatiotemporally monitor Col1 and Col2 gene expression, histology, and biomechanics up to 8 weeks following a full-length patellar tendon injury. Gene expression and histology were analyzed weekly for up to 5 weeks while mechanical properties were measured at 1, 2, 5, and 8 weeks. At week 1, the healing region displayed loose granulation tissue with little Col1 expression. Col1 expression peaked at 2 weeks, but the ECM was highly disorganized and hypercellular. By 3 weeks, Col1 expression had reduced and by 5 weeks, the ECM was generally aligned along the tendon axis. Col2 expression was not seen in the healing midsubstance or insertion at any time point. The biomechanics of the healing tissue was inadequate at all time points, achieving ultimate loads and stiffnesses of 48% and 63% of normal values by 8 weeks. Future studies will further characterize the cells within the healing midsubstance and insertion using tenogenic markers and compare these results to those of tendon cells during normal development. (c) 2011 Orthopaedic Research Society Published by Wiley Periodicals, Inc. J Orthop Res 30:2836, 2012
引用
收藏
页码:28 / 36
页数:9
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