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Chemically defined and xeno-free culture condition for human extended pluripotent stem cells

Author

Listed:
  • Bei Liu

    (Peking University Health Science Center and the MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking-Tsinghua Center for Life Sciences, Peking University)

  • Shi Chen

    (Peking University Health Science Center and the MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking-Tsinghua Center for Life Sciences, Peking University)

  • Yaxing Xu

    (Peking University Health Science Center and the MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking-Tsinghua Center for Life Sciences, Peking University)

  • Yulin Lyu

    (Peking University)

  • Jinlin Wang

    (Peking University Health Science Center and the MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking-Tsinghua Center for Life Sciences, Peking University)

  • Yuanyuan Du

    (Peking University Health Science Center and the MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking-Tsinghua Center for Life Sciences, Peking University)

  • Yongcheng Sun

    (Bengbu Medical College)

  • Heming Liu

    (Peking University Health Science Center and the MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking-Tsinghua Center for Life Sciences, Peking University)

  • Haoying Zhou

    (Peking University Health Science Center and the MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking-Tsinghua Center for Life Sciences, Peking University)

  • Weifeng Lai

    (Peking University Health Science Center and the MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking-Tsinghua Center for Life Sciences, Peking University)

  • Anqi Xue

    (Peking University Health Science Center and the MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking-Tsinghua Center for Life Sciences, Peking University)

  • Ming Yin

    (Beijing Vitalstar Biotechnology)

  • Cheng Li

    (Peking University)

  • Yun Bai

    (Peking University Stem Cell Research Center, Peking University Health Science Center, Peking University)

  • Jun Xu

    (Peking University Stem Cell Research Center, Peking University Health Science Center, Peking University)

  • Hongkui Deng

    (Peking University Health Science Center and the MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking-Tsinghua Center for Life Sciences, Peking University)

Abstract

Extended pluripotent stem (EPS) cells have shown great applicative potentials in generating synthetic embryos, directed differentiation and disease modeling. However, the lack of a xeno-free culture condition has significantly limited their applications. Here, we report a chemically defined and xeno-free culture system for culturing and deriving human EPS cells in vitro. Xeno-free human EPS cells can be long-term and genetically stably maintained in vitro, as well as preserve their embryonic and extraembryonic developmental potentials. Furthermore, the xeno-free culturing system also permits efficient derivation of human EPS cells from human fibroblast through reprogramming. Our study could have broad utility in future applications of human EPS cells in biomedicine.

Suggested Citation

  • Bei Liu & Shi Chen & Yaxing Xu & Yulin Lyu & Jinlin Wang & Yuanyuan Du & Yongcheng Sun & Heming Liu & Haoying Zhou & Weifeng Lai & Anqi Xue & Ming Yin & Cheng Li & Yun Bai & Jun Xu & Hongkui Deng, 2021. "Chemically defined and xeno-free culture condition for human extended pluripotent stem cells," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-23320-8
    DOI: 10.1038/s41467-021-23320-8
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