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TISSUE-SPECIFIC STEM CELLS

Matrix Metalloprotease Activity Is an Essential Link Between Mechanical Stimulus and Mesenchymal Stem Cell Behavior

^aMusculoskeletal Research Center Berlin, Charité - Universitätsmedizin, Berlin, Germany;
^bBerlin-Brandenburg Center for Regenerative Therapies, Charité - Universitätsmedizin, Berlin, Germany;
^cFree University Berlin, Department of Biology, Chemistry, Pharmacy, Berlin, Germany

Key Words. Matrix metalloproteinases • Adult stem cells • Regeneration • Mechanical stimulation

Correspondence: Grit Kasper, Ph.D., Musculoskeletal Research Center Berlin, Charité - Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany. Telephone: ++49-30-450 615116; Fax: ++49-30-450 559969; e-mail: Grit.Kasper{at}charite.de

Received on October 23, 2006; accepted for publication on April 27, 2007.

First published online in STEM CELLS EXPRESS  May 10, 2007.


Progenitor cells are involved in the regeneration of the musculoskeletal system, which is known to be influenced by mechanical boundary conditions. Furthermore, matrix metalloproteases (MMPs) and tissue-specific inhibitors of metalloproteases (TIMPs) are crucial for matrix remodelling processes that occur during regeneration of bone and other tissues. This study has therefore investigated whether MMP activity affects mesenchymal stem cell (MSC) behavior and how MMP activity is influenced by the mechanical stimulation of these cells. Broad spectrum inhibition of MMPs altered the migration, proliferation, and osteogenic differentiation of MSCs. Expression analysis detected MMP-2, -3, -10, -11, -13, and -14, as well as TIMP-2, in MSCs at the mRNA and protein levels. Mechanical stimulation of MSCs led to an upregulation of their extracellular gelatinolytic activity, which was consistent with the increased protein levels seen for MMP-2, -3, -13, and TIMP-2. However, mRNA expression levels of MMPs/TIMPs showed no changes in response to mechanical stimulation, indicating an involvement of post-transcriptional regulatory processes such as alterations in MMP secretion or activation. One potential regulatory molecule might be the furin protease. Specific inhibition of MMP-2, -3, and -13 showed MMP-13 to be involved in osteogenic differentiation. The results of this study suggest that MSC function is controlled by MMP activity, which in turn is regulated by mechanical stimulation of cells. Thus, MMP/TIMP balance seems to play an essential role in transferring mechanical signals into MSC function.

Disclosure of potential conflicts of interest is found at the end of this article.

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