Cryopreservation of Hepatocyte Organoid-Derived Cells Generated from Human iPS Cells

Hepatic organoids (iHOs) generated from human-induced pluripotent stem cell-derived hepatocyte-like cells (HLCs) have attracted attention as a new source of hepatocytes to replace primary human hepatocytes (PHHs) in drug discovery research. Recently, we established iHOs from HLCs, which proliferated for more than 10 passages, and developed a two-dimensional (2D) culture protocol for iHOs, by which the cells showed much higher hepatic functions. In this study, we examined the cryopreservation of iHOs for the purpose of improving their versatility. Cryopreserved iHOs had comparable cell proliferative capacity to fresh iHOs. Hepatocyte marker gene expression levels in the cryopreserved iHOs were comparable to those without cryopreservation. When cryopreserved iHOs were directly matured by our 2D culture protocol, they showed higher hepatocyte marker gene expression levels and higher CYP3A4 activity than HLCs. Some of the hepatic functions in 2D-cultured cryopreserved iHOs were at levels comparable to those in PHHs. These results suggest that cryopreserved iHOs also differentiated into mature hepatocytes by 2D culture. We expect cryopreserved iHOs to be used as a user-friendly cell source for drug discovery research in many laboratories.

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Publication Details

Journal
Biological and Pharmaceutical Bulletin
Published
2025-09-16
DOI
https://doi.org/10.1248/bpb.b25-00276
Primary Topic
Liver physiology and pathology
Type
article
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article

Cryopreservation of Hepatocyte Organoid-Derived Cells Generated from Human iPS Cells

Hiroyuki Mizuguchi, Yukiko Ueyama-Toba, Jumpei Inui, Rei Asano et al.
Biological and Pharmaceutical Bulletin
Liver physiology and pathology
article

Cryopreservation of Hepatocyte Organoid-Derived Cells Generated from Human iPS Cells

Hiroyuki Mizuguchi, Yukiko Ueyama-Toba, Jumpei Inui, Rei Asano, Wakana Nagai
article en

Abstract

Hepatic organoids (iHOs) generated from human-induced pluripotent stem cell-derived hepatocyte-like cells (HLCs) have attracted attention as a new source of hepatocytes to replace primary human hepatocytes (PHHs) in drug discovery research. Recently, we established iHOs from HLCs, which proliferated for more than 10 passages, and developed a two-dimensional (2D) culture protocol for iHOs, by which the cells showed much higher hepatic functions. In this study, we examined the cryopreservation of iHOs for the purpose of improving their versatility. Cryopreserved iHOs had comparable cell proliferative capacity to fresh iHOs. Hepatocyte marker gene expression levels in the cryopreserved iHOs were comparable to those without cryopreservation. When cryopreserved iHOs were directly matured by our 2D culture protocol, they showed higher hepatocyte marker gene expression levels and higher CYP3A4 activity than HLCs. Some of the hepatic functions in 2D-cultured cryopreserved iHOs were at levels comparable to those in PHHs. These results suggest that cryopreserved iHOs also differentiated into mature hepatocytes by 2D culture. We expect cryopreserved iHOs to be used as a user-friendly cell source for drug discovery research in many laboratories.

Biological and Pharmaceutical BulletinVol. 48(9)
National Institute of Biomedical Innovation, Health and Nutrition (JP), Osaka University Hospital (JP), Osaka University of Pharmaceutical Sciences (JP), The University of Osaka (JP)
Openalex Percentile: Top 66%
Liver physiology and pathology
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