Differentiation of human adipose stromal cells into hepatic lineage in vitro and in vivo
Abstract
Embryonic stem cells (ES cells), bone marrow-derived mesenchymal stem cells, umbilical cord blood-derived mesenchymal stem cells, and hepatic stem cells in liver have been known as a useful source that can induce to differentiate into hepatocytes. In this study, we examined whether human adipose tissue-derived stromal cells (hADSC) can differentiate into hepatic lineage in vitro. hADSC, that were induced to differentiate into hepatocyte-like cells by the treatment of HGF and OSM, had morphology similar to hepatocytes. Addition of DMSO enhanced differentiation into hepatocytes. RT-PCR and immunocytochemical analysis showed that hADSC express albumin and alpha-fetoprotein during differentiation. Differentiated hADSC showed LDL uptake and production of urea. Additionally, transplanted hADSC to CCl4-injured SCID mouse model were able to be differentiated into hepatocytes and they expressed albumin in vivo. Mesenchymal stem cells isolated from human adipose tissue are immunocompatible and are easily isolated. Therefore, hADSC may become an alternative source to hepatocyte regeneration or liver cell transplantation.
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MSCs derived from various sources can differentiate into functional HLCs along the endodermal lineage under both in vitro and in vivo conditions in experimental animal models and humans.
“It has been reported in experimental animal models and humans that MSCs derived from various sources can differentiate into functional HLCs along the endodermal lineage under both in vitro and in vivo conditions [90–92].”
From Mechanisms, efficacy, and future perspectives of cellular-based therapies for liver fibrosis/cirrhosis: focusing on mesenchymal stromal cells (2025) · cites this paper as [92]
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“It has been reported in experimental animal models and humans that MSCs derived from various sources can differentiate into functional HLCs along the endodermal lineage under both in vitro and in vivo conditions [90–92].”
- Authors
- Seo, M. J., Suh, S. Y., Bae, Y. C., & Jung, J. S.
- Affiliations
- Pusan National University (KR)
- Dong-A University (KR)
- Corresponding author
- Jung, Jin Sup
- Venue
- Biochemical and Biophysical Research Communications
- Publisher
- Elsevier BV
- Published
- 2005-03
- Volume
- 328
- Issue
- 1
- Pages
- 258-264
- ISSN
- 0006-291X (ISSN-L)
- OpenAlex
- W2118458879
- Cited by
- 530
- References
- 0
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 12 · 2023: 9 · 2022: 13 · 2021: 10 · 2020: 18 · 2019: 22 · 2018: 22 · 2017: 19 · 2016: 20 · 2015: 31 · 2014: 39 · 2013: 44 · 2012: 40
- FWCI
- 15.19
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biochemical and Biophysical Research Communications (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Keywords
- adipose-derived stromal cells, hepatocyte differentiation, hepatocyte-like cells, hepatocyte regeneration, hepatocyte transplantation, hepatocyte growth factor, albumin, alpha-fetoprotein, LDL uptake, urea synthesis, carbon tetrachloride-induced liver injury, SCID mice, mesenchymal stem cells
- MeSH terms
- Adult, Animals, Cell Differentiation, Dimethyl Sulfoxide, Female, Humans, Lipoproteins, LDL, Male, Middle Aged, Peptides, Urea, Mice, SCID, Mice, Inbred NOD, Stromal Cells, Hepatocyte Growth Factor, Adipocytes, Hepatocytes, Cell Size, Mice, Oncostatin M
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