A defined glycosaminoglycan-binding substratum for human pluripotent stem cells

被引:196
作者
Klim, Joseph R. [1 ]
Li, Lingyin [2 ]
Wrighton, Paul J. [3 ]
Piekarczyk, Marian S. [4 ]
Kiessling, Laura L. [1 ,2 ,3 ]
机构
[1] Univ Wisconsin, Cell & Mol Biol Program, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Biochem, Madison, WI 53705 USA
[4] WiCell Res Inst, Madison, WI USA
基金
美国国家卫生研究院;
关键词
SELF-ASSEMBLED MONOLAYERS; SYNTHETIC SURFACES; RENEWAL; GROWTH; DIFFERENTIATION; SURVIVAL; INTEGRIN; ADHESION; RECEPTOR; CULTURE;
D O I
10.1038/NMETH.1532
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
To exploit the full potential of human pluripotent stem cells for regenerative medicine, developmental biology and drug discovery, defined culture conditions are needed. Media of known composition that maintain human embryonic stem (hESES) cells have been developed, but finding chemically defined, robust substrata has proven difficult. We used an array of self-assembled monolayers to identify peptide surfaces that sustain pluripotent stem cell self-renewal. The effective substrates displayed heparin-binding peptides, which can interact with cell-surface glycosaminoglycans and could be used with a defined medium to culture hESES cells for more than 3 months. The resulting cells maintained a normal karyotype and had high levels of pluripotency markers. The peptides supported growth of eight pluripotent cell lines on a variety of scaffolds. Our results indicate that synthetic substrates that recognize cell-surface glycans can facilitate the long-term culture of pluripotent stem cells.
引用
收藏
页码:989 / U72
页数:8
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