Long-term self-renewal of human pluripotent stem cells on peptide-decorated poly(OEGMA-co-HEMA) brushes under fully defined conditions

基质凝胶 诱导多能干细胞 干细胞 细胞生物学 组织工程 材料科学 间充质干细胞 细胞粘附 细胞生长 化学 纳米技术 细胞 生物医学工程 生物 生物化学 胚胎干细胞 医学 基因
作者
Xiaohua Deng,X. Y. Zhang,Xiu Song Zhao,Q. J. Li,Zhenyu Ye,Z. B. Li,Y. W. Liu,Y. Zhou,Hong Ma,Genhua Pan,Deqing Pei,J. Fang,Su-Huai Wei
出处
期刊:Acta Biomaterialia [Elsevier]
卷期号:9 (11): 8840-8850 被引量:45
标识
DOI:10.1016/j.actbio.2013.07.017
摘要

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.
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