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    Generation of small molecules

    derived hepatic stem cells
    Human primary hepatocytes were reprogrammed
    towards hepatic progenitor
    cells by a combined treatment with 2
    small molecules, A83-01 and CHIR99021,
    and HGF. Chemically derived hepatic progenitors
    exhibited a high proliferation
    potential and the ability to differentiate
    into hepatocytes and biliary epithelial
    cells both in vitro and in vivo. This
    approach enables the generation of
    patient-specific hepatic progenitors and
    provides a platform for personal and stem
    cell-based regenerative medicine.

    Skeletal Muscle

    Regeneration


    Pharmacological inhibition of myostatin/TGFb receptor/pSmad3

    signaling rescues muscle

    regnerative responses in mouse

    model of type 1 diabetes.

    Skeletal Muscle

    Atrophy


    Fbxw7b is an inducing mediator of dexamethasone-induced

    skeletal muscle atrophy

    in vivo with the axis of

    Fbxw7b-myogenin-atrogenes.

    Skeletal muscle

    Dystrophy


    Patient-tailored application

    for Duchene muscular dystrophy

    on mdx mice based induced

    mesenchymal stem cells

    3D bio-printing

    Three-dimensional (3D) bioprinting technology is a promising new technology in the field

    of bioartificial organ generation with regard to overcoming the limitations of organ supply. 

    Isolated primary hepatocytes from the liver are very similar to in vivo native liver
    hepatocytes, but they have the disadvantage of a limited lifespan in 2D culture. Although a sandwich
    culture and 3D organoids with mesenchymal stem cells (MSCs) as an attractive assistant cell source
    to extend lifespan can be used, it cannot fully reproduce the in vivo architecture. Moreover, longterm
    3D culture leads to cell death because of hypoxic stress. Therefore, to overcome the drawback
    of 2D and 3D organoids, we try to use a 3D printing technique using alginate hydrogels with primary
    hepatocytes and MSCs.

    Hepatocytes differentiation from hiPSCs

    Pluripotent stem cells can differentiate into many cell types including mature hepatocytes, and can be used in the development of new drugs, treatment of diseases,

    and in basic research. Producing hepatocytes using stem cells helps to avoid the need to purify primary hepatocytes from donor livers.

    We propose to generate HLCs from patients and normal individuals with the protocols.

    We have developed and examined their behavior when transplanted into a mouse liver damaged model.

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