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Effects of matrix metalloproteinase-1 on the myogenic differentiation of bone marrow-derived mesenchymal stem cells in vitro

  • Zhenyang Zheng
    ,
  • Yan Leng
    ,
  • Chen Zhou
    ,
  • Zhenyu Ma
    ,
  • Zhigang Zhong
    ,
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Matrix metalloproteinase-1 (MMP-1) is a member of the family of zinc-dependent endopeptidases that are capable of degrading extracellular matrix (ECM) and certain non-matrix proteins. It has been shown that MMP-1 can enhance muscle regeneration by improving the differentiation and migration of myoblasts. However, it is still not known whether MMP-1 can promote the myogenesis of bone marrow-derived mesenchymal stem cells (BMSCs). To address this question, we isolated BMSCs from C57BL/6J mice and investigated the effects of MMP-1 on their proliferation and myogenic differentiation. Our results showed that MMP-1 treatment, which had no cytotoxic effects on BMSCs, increased the mRNA and protein levels of MyoD and desmin in a dose-dependent manner, indicating that MMP-1 promoted myogenic differentiation of BMSCs in vitro. These results suggest that BMSCs may have a therapeutic potential for treating muscular disorders.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 309-314 (6 pages)

Journal (Volume, Issue Number)

Biochemical and Biophysical Research Communications (Volume 428, Issue 2)

Publication milestones

  • Published - 11/16/2012

Publication status

Published - 11/16/2012

ISSN

0006-291X

Publication IDs

  • Scopus: 84869204630
  • PubMed: 23085232

Publication metrics

Metrics

SciVal
citations
7
SciVal
FWCI
0.26
SciVal
Author count
7
SciVal
Paper percentile
59
Scopus
citations
Fractional count
1
Fractional count
0.14
Fractional count
6
Fractional count
0.86
Fractional count
1
Fractional count
1

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Citation count
6
Captures
9

Funding Details

We thank Lei Wei and Dingbang Chen for their excellent technical assistance. This study was supported by the National Natural Science Foundation of China (Grant Nos. 30971026 and 30870852 ).
FunderFunding numbers
NSFC
30870852, 30971026