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
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.