Matrix metalloproteinase-1 therapy improves muscle healing

被引:45
作者
Bedair, Hany
Liu, T. Thomas
Kaar, Joel L.
Badlani, Shawn
Russell, Alan J.
Li, Yong
Huard, Johnny
机构
[1] Univ Pittsburgh, Childrens Hosp Pittsburgh, Stem Cell Res Ctr, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Orthopaed Surg, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, McGowan Inst Regenerat Med, Dept Surg, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Dept Pathol, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Dept Mol Genet & Biochem, Pittsburgh, PA 15213 USA
关键词
muscle injury; fibrosis; regeneration;
D O I
10.1152/japplphysiol.00670.2006
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Muscle undergoes time-dependent phases of healing after injury, which ultimately results in residual fibrosis in the injured area. The use of exogenous matrix metalloproteinases (MMPs) may improve recovery after muscle injury by promoting the digestion of existing fibrous tissue and releasing local growth factors. In the current experiment, bilateral gastrocnemius (GM) lacerations were created in severe combined immunodeficient mice. Twenty-five days after injury (peak posttraumatic fibrosis), C2C12 cells (myoblasts) transduced with the LacZ reporter gene were injected with exogenous MMP-1 into the right GMs at the site of injury; the cells were also injected along with PBS (control) at the site of injury in the left GMs. The muscle tissues were examined histologically via X-gal, hemotoxylin and eosin, and Masson's trichrome staining. The MMP-treated limbs contained more regenerating myofibers than did the control limbs (MMP 170 +/- 96 fibers, control 62 51 fibers; P < 0.001). Less fibrous tissue was observed within MMP-treated muscles (MMP: 24 +/- 11%, control: 35 +/- 15%; P < 0.01). These results suggest that the direct injection of MMP-1 into the zone of injury during fibrosis can enhance muscle regeneration by increasing the number of myofibers and decreasing the amount of fibrous tissue.
引用
收藏
页码:2338 / 2345
页数:8
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