| Literature DB >> 23891809 |
Y Deng1, X Zhang, X Zhao, Q Li, Z Ye, Z Li, Y Liu, Y Zhou, H Ma, G Pan, D Pei, J Fang, S Wei.
Abstract
Realization of the full potential of human induced pluripotent stem cells (hiPSC) in clinical applications requires the development of well-defined culture conditions for their long-term growth and directed differentiation. This paper describes a novel fully defined synthetic peptide-decorated substrate that supports self-renewal of hiPSC in commercially available xeno-free, chemically defined medium. The Au surface was deposited by a poly(OEGMA-co-HEMA) film, using the surface-initiated polymerization method (SIP) with the further step of carboxylation. The hiPSC generated from umbilical cord mesenchymal cells were successfully cultured for 10 passages on the peptide-tethered poly(OEGMA-co-HEMA) brushes for the first time. Cells maintained their characteristic morphology, proliferation and expressed high levels of markers of pluripotency, similar to the cells cultured on Matrigel™. Moreover, the cell adhesion could be tuned by the pattern and peptide concentration on the substrate. This well-defined, xeno-free and safe substrate, which supports long-term proliferation and self-renewal of hiPSC, will not only help to accelerate the translational perspectives of hiPSC, but also provide a platform to elucidate the underlying molecular mechanisms that regulate stem cell proliferation and differentiation via SIP technology.Entities:
Keywords: Human pluripotent stem cell; Long-term; Peptide; Self-renewal; Surface-initiated polymerization
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Year: 2013 PMID: 23891809 DOI: 10.1016/j.actbio.2013.07.017
Source DB: PubMed Journal: Acta Biomater ISSN: 1742-7061 Impact factor: 8.947