Author/Authors :
Deng، نويسنده , , Y. and Zhang، نويسنده , , X. and Zhao، نويسنده , , X. and Li، نويسنده , , Q. and Ye، نويسنده , , Z. and Li، نويسنده , , Z. and Liu، نويسنده , , Y. and Zhou، نويسنده , , Y. and Ma، نويسنده , , H. and Pan، نويسنده , , G. and Pei، نويسنده , , D. and Fang، نويسنده , , J. and Wei، نويسنده , , S.، نويسنده ,
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.
Keywords :
long-term , Peptide , Self-Renewal , surface-initiated polymerization , Human pluripotent stem cell