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Using Human Induced Pluripotent Stem Cell-derived Hepatocyte-like Cells for Drug Discovery
Published on: May 19, 2018
A preliminary study for constructing a bioartificial liver device with induced pluripotent stem cell-derived
Masaya Iwamuro1, Hidenori Shiraha, Shuhei Nakaji
1Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama, Japan. iwamuromasaya@yahoo.co.jp
Biomedical Engineering Online
|December 11, 2012
Summary
This study demonstrates that induced pluripotent stem (iPS) cells can be differentiated into functional hepatocyte-like cells for bioartificial liver systems, overcoming immunological rejection concerns and showing promise for liver failure treatment.
Area of Science:
- Biomedical Engineering
- Tissue Engineering
- Regenerative Medicine
Background:
- Bioartificial liver systems aim to support patients with liver failure using bioreactors and hepatocytes.
- Immunological rejection of hepatocytes is a major challenge, limiting device performance.
- Patient-derived induced pluripotent stem (iPS) cells offer a solution to immunological rejection in bioartificial liver systems.
Purpose of the Study:
- To evaluate the feasibility of a bioartificial liver system utilizing iPS cell-derived hepatocyte-like cells.
- To assess the differentiation potential and functionality of iPS cells into hepatocyte-like cells for liver support.
Main Methods:
- Mouse iPS cells were differentiated into hepatocyte-like cells through embryoid bodies and definitive endoderm.
- Differentiation was confirmed via morphology, PCR, and functional assays.
- iPS cell-derived hepatocytes were cultured in a 0.2 μm pore bioreactor for 7 days, with albumin secretion measured by ELISA.
Main Results:
- Differentiated iPS cells exhibited hepatocyte morphology, including glycogen deposition and microvilli.
- Increased albumin mRNA expression and functional albumin and urea production were observed.
- Albumin accumulated in the bioreactor medium over 7 days, indicating sustained function.
Conclusions:
- Combining a 0.2-μm pore bioreactor with iPS cell-derived hepatocytes is a promising strategy for bioartificial liver systems.
- This study provides foundational data for developing iPS cell-based bioartificial liver technologies.
- The approach addresses immunological rejection, paving the way for improved liver support devices.

