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Volume 6, Issue 8, Pages 2920-2931 (August 2010)


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Effects of TGF-β3 and preculture period of osteogenic cells on the chondrogenic differentiation of rabbit marrow mesenchymal stem cells encapsulated in a bilayered hydrogel composite

X. Guoa, J. Liaob, H. Parkb, A. Sarafb, R.M. Raphaelb, Y. Tabatac, F.K. Kasperb, A.G. MikosabCorresponding Author Informationemail address

Received 17 November 2009; received in revised form 23 February 2010; accepted 24 February 2010. published online 02 March 2010.

Abstract 

In this work, injectable, biodegradable hydrogel composites of crosslinked oligo(poly(ethylene glycol) fumarate) and gelatin microparticles (MPs) were used to fabricate a bilayered osteochondral construct. Rabbit marrow mesenchymal stem cells (MSCs) were encapsulated with transforming growth factor-β3 (TGF-β3)-loaded MPs in the chondrogenic layer and cocultured with cells of different periods of osteogenic preculture (0, 3, 6 and 12days) in the osteogenic layer to investigate the effects of TGF-β3 delivery and coculture on the proliferation and differentiation of cells in both layers. The results showed that, in the chondrogenic layer, TGF-β3 significantly stimulated chondrogenic differentiation of MSCs. In addition, cells of various osteogenic preculture periods in the osteogenic layer, along with TGF-β3, enhanced gene expression for MSC chondrogenic markers to different extents. In the osteogenic layer, cells maintained their alkaline phosphatase activity during the coculture; however, mineralization was delayed by the presence of TGF-β3. Overall, this study demonstrated the fabrication of bilayered hydrogel composites which mimic the structure and function of osteochondral tissue, along with the application of these composites as cell and growth factor carriers, while illustrating that encapsulated cells of different degrees of osteogenic differentiation can significantly influence the chondrogenic differentiation of cocultured progenitor cells in both the presence and absence of chondrogenic growth factors.

a Department of Chemical and Biomolecular Engineering, Rice University, MS-362, PO Box 1892, Houston, TX 77251-1892, USA

b Department of Bioengineering, Rice University, MS-142, PO Box 1892, Houston, TX 77251-1892, USA

c Department of Biomaterials, Field of Tissue Engineering, Institute for Frontier Medical Sciences, Kyoto University, 53 Kawara-cho Shogoin, Sakyo-ku, Kyoto 606-8507, Japan

Corresponding Author InformationCorresponding author. Address: Department of Bioengineering, Rice University, MS-142, PO Box 1892, Houston, TX 77251-1892, USA. Tel.: +1 713 3485355; fax: +1 713 3484244.

PII: S1742-7061(10)00120-0

doi:10.1016/j.actbio.2010.02.046


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