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a Interdisciplinary Center for Clinical Research on Biomaterials, IZKF BIOMAT, Aachen, Germany;
b Institute of Pathology, University Hospital, Aachen, Germany
Key Words. HGF • Mesenchymal stem cells • Cell migration • Mobilization
Willi Jahnen-Dechent, Ph.D., IZKF BIOMAT, University Hospital, Pauwelsstrasse 30, D-52074 Aachen, Germany. Telephone: 49-241-80-80163; Fax: 49-241-80-82573; e-mail: willi.jahnen{at}rwth-aachen.de
Human mesenchymal stem cells (hMSC) are adult stem cells with multipotent capacities. The ability of mesenchymal stem cells to differentiate into many cell types, as well as their high ex vivo expansion potential, makes these cells an attractive therapeutic tool for cell transplantation and tissue engineering. hMSC are thought to contribute to tissue regeneration, but the signals governing their mobilization, diapedesis into the bloodstream, and migration into the target tissue are largely unknown. Here we report that hepatocyte growth factor (HGF) and the cognate receptor HGFR/c-met are expressed in hMSC, on both the RNA and the protein levels. The expression of HGF was downregulated by transforming growth factor beta. HGF stimulated chemotactic migration but not proliferation of hMSC. Therefore the HGF/c-met signaling system may have an important role in hMSC recruitment sites of tissue regeneration. The controlled regulation of HGF/c-met expression may be beneficial in tissue engineering and cell therapy employing hMSC.
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