New Insights into Osteogenic and Chondrogenic Differentiation of Human Bone Marrow Mesenchymal Stem Cells and Their Potential Clinical Applications for Bone Regeneration in Pediatric Orthopaedics

Human mesenchymal stem cells (hMSCs) are pluripotent adult stem cells capable of being differentiated into osteoblasts, adipocytes, and chondrocytes. The osteogenic differentiation of hMSCs is regulated either by systemic hormones or by local growth factors able to induce specific intracellular sign...

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Published in:Stem Cells International Vol. 2013; no. 2013; pp. 137 - 147
Main Authors: Lisignoli, Gina, Giuliani, Nicola, Magnani, Marina, Racano, Costantina, Bolzoni, Marina, Dalla Palma, Benedetta, Spolzino, Angelica, Manferdini, Cristina, Abati, Caterina, Toscani, Denise, Facchini, Andrea, Aversa, Franco
Format: Journal Article
Language:English
Published: Cairo, Egypt Hindawi Limiteds 01-01-2013
Hindawi Puplishing Corporation
Hindawi Publishing Corporation
John Wiley & Sons, Inc
Hindawi Limited
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Summary:Human mesenchymal stem cells (hMSCs) are pluripotent adult stem cells capable of being differentiated into osteoblasts, adipocytes, and chondrocytes. The osteogenic differentiation of hMSCs is regulated either by systemic hormones or by local growth factors able to induce specific intracellular signal pathways that modify the expression and activity of several transcription factors. Runt-related transcription factor 2 (Runx2) and Wnt signaling-related molecules are the major factors critically involved in the osteogenic differentiation process by hMSCs, and SRY-related high-mobility-group (HMG) box transcription factor 9 (SOX9) is involved in the chondrogenic one. hMSCs have generated a great interest in the field of regenerative medicine, particularly in bone regeneration. In this paper, we focused our attention on the molecular mechanisms involved in osteogenic and chondrogenic differentiation of hMSC, and the potential clinical use of hMSCs in osteoarticular pediatric disease characterized by fracture nonunion and pseudarthrosis.
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Academic Editor: Paul T. Sharpe
ISSN:1687-966X
1687-9678
1687-9678
DOI:10.1155/2013/312501