Evidence map›Paper›PMID 42759067›Full record

ArticleStem cells translational medicine2026

Fate of long-term culture on hepatocyte-like cells generated from human adipose-derived mesenchymal stem cells.

Mengling Ji, Yu Saito, Yuhei Waki, Shuhai Chen, Tetsuya Ikemoto, Takayuki Noma, Hiroki Teraoku, Shinichiro Yamada, Yuji Morine, Mitsuo Shimada

Abstract read
In one paragraph

Article in Stem cells translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Mengling JiDepartment of Surgery, Tokushima University, Tokushima, 770-8503, Japan.ORCID 0009-0004-3554-5542
Yu SaitoDepartment of Surgery, Tokushima University, Tokushima, 770-8503, Japan.ORCID 0000-0001-6349-1669
Yuhei WakiDepartment of Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Shuhai ChenDepartment of Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Tetsuya IkemotoDepartment of Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Takayuki NomaDepartment of Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Hiroki TeraokuDepartment of Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Shinichiro YamadaDepartment of Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Yuji MorineDepartment of Surgery, Tokushima University, Tokushima, 770-8503, Japan.
Mitsuo ShimadaDepartment of Surgery, Tokushima University, Tokushima, 770-8503, Japan.

Funding

AMED S0-424003-00Center for Clinical and Translational Research of Kyushu University
6 · The paper itself

Abstract

backgroundWe previously established a 21-day protocol to generate hepatocyte-like cells (HLCs) from adipose-derived stem cells and are conducting preclinical studies toward their clinical application in liver failure. This study examined how long HLCs maintain viability and hepatocyte-specific functions after differentiation.

methodsAdipose-derived stem cells (2.0 × 106) were differentiated into HLCs using a 3-step protocol for 21 days. After differentiation, cells were either transferred to transplantation medium (TM), used clinically, or maintained in step-3 differentiation medium (DM). Cell viability, hepatocyte-specific gene expression, and functional assays were performed on days 24 and 28. Because bile acid synthesis may induce cytotoxicity during extended culture, the expression of bile acid-related genes and transporters was evaluated on day 35.

resultsViability markedly decreased when HLCs were transferred to TM, whereas cells maintained in DM preserved viability up to day 28. The expression of mature hepatocyte markers (AAT, ALB, CPS1, and OTC) remained comparable between days 21 and 28. Hepatocyte functions, including CYP3A4 activity and ammonia metabolism, were also sustained in DM-cultured HLCs. Importantly, genes involved in bile acid synthesis and transport, which could contribute to cytotoxicity during prolonged culture, were undetectable even after 28 days.

conclusionHLCs generated using our protocol maintained viability and hepatocyte-specific functions for at least 28 days when cultured in DM, without detectable bile acid-related gene expression. These findings suggest that transplantation timing can be flexibly adjusted for at least 1 week after the completion of differentiation.

Indexed as

Adipose TissueCell Culture TechniquesCell DifferentiationHepatocytesMesenchymal Stem CellsBile Acids and SaltsCells, CulturedCell SurvivalHumansBile Acids and Saltsadipose-derived mesenchymal stem cellsbile acidhepatocyte-like cellslong-term culture

Identifiers

PMID42759067
PMCPMC13588577

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.