Biocompatibility of synthetic poly(ester urethane)/polyhedral oligomeric silsesquioxane matrices with embryonic stem cell proliferation and differentiation
- 8 March 2010
- journal article
- research article
- Published by Hindawi Limited in Journal of Tissue Engineering and Regenerative Medicine
- Vol. 4 (7) , 553-564
- https://doi.org/10.1002/term.272
Abstract
Incorporation of polyhedral oligomeric silsesquioxanes (POSS) into poly(ester urethanes) (PEU) as a building block results in a PEU/POSS hybrid polymer with increased mechanical strength and thermostability. An attractive feature of the new polymer is that it forms a porous matrix when cast in the form of a thin film, making it potentially useful in tissue engineering. In this study, we present detailed microscopic analysis of the PEU/POSS matrix and demonstrate its biocompatibility with cell culture. The PEU/POSS polymer forms a continuous porous matrix with open pores and interconnected grooves. From SEM image analysis, it is calculated that there are about 950 pores/mm2 of the matrix area with pore diameter size in the range 1–15 µm. The area occupied by the pores represents approximately 7.6% of the matrix area. Using mouse embryonic stem cells (ESCs), we demonstrate that the PEU/POSS matrix provides excellent support for cell proliferation and differentiation. Under the cell culture condition optimized to maintain self‐renewal, ESCs grown on a PEU/POSS matrix exhibit undifferentiated morphology, express pluripotency markers and have a similar growth rate to cells grown on gelatin. When induced for differentiation, ESCs underwent dramatic morphological change, characterized by the loss of clonogenecity and increased cell size, with well‐expanded cytoskeleton networks. Differentiated cells are able to form a continuous monolayer that is closely embedded in the matrix. The excellent compatibility between the PEU/POSS matrix and ESC proliferation/differentiation demonstrates the potential of using PEU/POSS polymers in future ESC‐based tissue engineering. Copyright © 2010 John Wiley & Sons, Ltd.Keywords
This publication has 30 references indexed in Scilit:
- Mouse embryonic stem cells lacking p38α and p38δ can differentiate to endothelial cells, smooth muscle cells, and epithelial cellsDifferentiation, 2009
- Biomaterials for stem cell differentiationAdvanced Drug Delivery Reviews, 2007
- Controlled differentiation of stem cellsAdvanced Drug Delivery Reviews, 2007
- Hyaluronic acid hydrogel for controlled self-renewal and differentiation of human embryonic stem cellsProceedings of the National Academy of Sciences, 2007
- Biomaterials Approach to Expand and Direct Differentiation of Stem CellsMolecular Therapy, 2007
- Altered Cell Adhesion and Cell Viability in a p38αMitogen-Activated Protein Kinase-Deficient Mouse Embryonic Stem Cell LineStem Cells and Development, 2006
- The Role of Biomaterials in Stem Cell Differentiation: Applications in the Musculoskeletal SystemStem Cells and Development, 2006
- Effects of Three-Dimensional Culture and Growth Factors on the Chondrogenic Differentiation of Murine Embryonic Stem CellsThe International Journal of Cell Cloning, 2005
- Effects of adsorbed heat labile serum proteins and fibrinogen on adhesion and apoptosis of monocytes/macrophages on biomaterialsJournal of Materials Science: Materials in Medicine, 2003
- Deficiency of the Stress Kinase P38α Results in Embryonic LethalityThe Journal of Experimental Medicine, 2000