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Osteogenic differentiation of human mesenchymal stem cells on poly(ethylene glycol)‐variant biomaterials
Author(s) -
Briggs Tonye,
Treiser Matthew D.,
Holmes Paul F.,
Kohn Joachim,
Moghe Prabhas V.,
Arinzeh Treena Livingston
Publication year - 2008
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.32310
Subject(s) - mesenchymal stem cell , peg ratio , ethylene glycol , materials science , alkaline phosphatase , tissue engineering , osteocalcin , microbiology and biotechnology , cell adhesion , adhesion , cell culture , protein adsorption , cellular differentiation , cell growth , motility , biomedical engineering , biophysics , chemistry , biochemistry , biology , polymer , medicine , enzyme , organic chemistry , genetics , finance , gene , economics , composite material
This study evaluated the osteogenic differentiation of human mesenchymal stem cells (MSCs), on tyrosine‐derived polycarbonates copolymerized with poly(ethylene glycol) (PEG) to determine their potential as a scaffold for bone tissue engineering applications. The addition of PEG in the backbone of polycarbonates has been shown to alter mechanical properties, degradation rates, degree of protein adsorption, and subsequent cell adhesion and motility in mature cell phenotypes. Its effect on MSC behavior is unknown. MSC morphology, motility, proliferation, and osteogenic differentiation were evaluated on polycarbonates containing 0–5% PEG over a 14 day culture. MSCs on polycarbonates containing 0% or 3% PEG content upregulated the expression of osteogenic markers as demonstrated by alkaline phosphatase activity and osteocalcin expression although at different stages in the 14 day culture. Cells on polycarbonates containing no PEG were characterized as having early onset of cell spreading and osteogenic differentiation. Cells on 3% PEG surfaces were delayed in cell spreading and osteogenic differentiation, but had the highest motility as compared with cells on substrates containing no PEG and substrates containing 5% PEG at early time points. Throughout the culture, cells on polycarbonates containing 5% PEG had the lowest levels of osteogenic markers, displayed poor cell‐substrate adhesion, and established cell‐cell aggregates. Thus, designing substrates with minute variations in PEG may serve as a tool to guide MSC adhesion and motility accompanying osteogenic differentiation, and may be beneficial for abundant bone tissue formation in vivo . © 2008 Wiley Periodicals, Inc. J Biomed Mater Res, 2009