4.3 Article

Cyclic loading inhibits expression of MMP-3 but not MMP-1 in an in vitro rabbit flexor tendon model

期刊

CLINICAL BIOMECHANICS
卷 23, 期 1, 页码 117-121

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.clinbiomech.2007.08.007

关键词

tendinopathy; overuse injury; organ culture; dynamic tissue loading; matrix metalloproteinase

资金

  1. NIOSH CDC HHS [R01 OH007359-04, OH007359-04] Funding Source: Medline
  2. NATIONAL INSTITUTE FOR OCCUPATIONAL SAFETY AND HEALTH [R01OH007359] Funding Source: NIH RePORTER

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Background. Gene expression analysis is useful for assessing cellular behavior and may improve our understanding of the initial cellular response to mechanical load leading to tendon degeneration. This study assessed gene expression of MMP-1 and MMP-3, genes associated with matrix degradation, in tendons exposed to cyclic loads within physiologic range. Methods. Six flexor tendons from each of ten New Zealand White rabbits were harvested and randomly assigned to one of the following six groups: load deprived for 18 h; cyclically loaded for 18 h to a peak stress of 2 MPa; 3 MPa; 4 MPa; 5 MPa; or snap frozen in liquid nitrogen. MMP-1, MMP-3 and 18 s mRNA expression was measured by qRT-PCR. Findings. No significant differences in MMP-1 mRNA expression levels were found between loading groups. MMP-3 expression was significantly inhibited (57%) in tendons cyclically loaded to a peak stress of 4 MPa in comparison to load deprived tendons, however, when peak stress was increased to 5 MPa, expression was no longer significantly lower compared to stress shielded tendons. Interpretation. The results suggest a 'U' shape relationship between load and MMP-3 expression. The lack of change in MMP-1 expression with loading was unexpected as inhibition of MMP-1 in response to mechanical load has been demonstrated in previous studies. In conclusion, we demonstrate that MMP-3 expression is modulated by cyclic load and is sensitive to load magnitude. MMP-1 mRNA expression is not significantly modulated by cyclic load in this model. (C) 2007 Elsevier Ltd. All rights reserved.

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