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Generation of functional ciliated cholangiocytes from human pluripotent stem cells

Author

Listed:
  • Mina Ogawa

    (University Health Network)

  • Jia-Xin Jiang

    (Programme in Molecular Medicine, Research Institute, Hospital for Sick Children)

  • Sunny Xia

    (Programme in Molecular Medicine, Research Institute, Hospital for Sick Children)

  • Donghe Yang

    (University Health Network)

  • Avrilynn Ding

    (University Health Network)

  • Onofrio Laselva

    (Programme in Molecular Medicine, Research Institute, Hospital for Sick Children)

  • Marcela Hernandez

    (University Health Network)

  • Changyi Cui

    (University Health Network)

  • Yuichiro Higuchi

    (Central Institute for Experimental Animals)

  • Hiroshi Suemizu

    (Central Institute for Experimental Animals)

  • Craig Dorrell

    (Oregon Health and Science University)

  • Markus Grompe

    (Oregon Health and Science University)

  • Christine E. Bear

    (Programme in Molecular Medicine, Research Institute, Hospital for Sick Children
    University of Toronto
    University of Toronto)

  • Shinichiro Ogawa

    (University Health Network
    University Health Network
    Shinshu University School of Medicine, Matsumoto
    University of Toronto)

Abstract

The derivation of mature functional cholangiocytes from human pluripotent stem cells (hPSCs) provides a model for studying the pathogenesis of cholangiopathies and for developing therapies to treat them. Current differentiation protocols are not efficient and give rise to cholangiocytes that are not fully mature, limiting their therapeutic applications. Here, we generate functional hPSC-derived cholangiocytes that display many characteristics of mature bile duct cells including high levels of cystic fibrosis transmembrane conductance regulator (CFTR) and the presence of primary cilia capable of sensing flow. With this level of maturation, these cholangiocytes are amenable for testing the efficacy of cystic fibrosis drugs and for studying the role of cilia in cholangiocyte development and function. Transplantation studies show that the mature cholangiocytes generate ductal structures in the liver of immunocompromised mice indicating that it may be possible to develop cell-based therapies to restore bile duct function in patients with biliary disease.

Suggested Citation

  • Mina Ogawa & Jia-Xin Jiang & Sunny Xia & Donghe Yang & Avrilynn Ding & Onofrio Laselva & Marcela Hernandez & Changyi Cui & Yuichiro Higuchi & Hiroshi Suemizu & Craig Dorrell & Markus Grompe & Christin, 2021. "Generation of functional ciliated cholangiocytes from human pluripotent stem cells," Nature Communications, Nature, vol. 12(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26764-0
    DOI: 10.1038/s41467-021-26764-0
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    1. Sonya A. MacParland & Jeff C. Liu & Xue-Zhong Ma & Brendan T. Innes & Agata M. Bartczak & Blair K. Gage & Justin Manuel & Nicholas Khuu & Juan Echeverri & Ivan Linares & Rahul Gupta & Michael L. Cheng, 2018. "Single cell RNA sequencing of human liver reveals distinct intrahepatic macrophage populations," Nature Communications, Nature, vol. 9(1), pages 1-21, December.
    2. Yuji Shiba & Sarah Fernandes & Wei-Zhong Zhu & Dominic Filice & Veronica Muskheli & Jonathan Kim & Nathan J. Palpant & Jay Gantz & Kara White Moyes & Hans Reinecke & Benjamin Van Biber & Todd Dardas &, 2012. "Human ES-cell-derived cardiomyocytes electrically couple and suppress arrhythmias in injured hearts," Nature, Nature, vol. 489(7415), pages 322-325, September.
    3. Johanna R. Schaub & Kari A. Huppert & Simone N. T. Kurial & Bernadette Y. Hsu & Ashley E. Cast & Bryan Donnelly & Rebekah A. Karns & Feng Chen & Milad Rezvani & Hubert Y. Luu & Aras N. Mattis & Anne-L, 2018. "De novo formation of the biliary system by TGFβ-mediated hepatocyte transdifferentiation," Nature, Nature, vol. 557(7704), pages 247-251, May.
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