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Liver Stem Cells: Experimental Findings and Implications for Human Liver Disease
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Evidence from human histopathology and experimental studies with rodents and zebrafish has shown that hepatocytes and cholangiocytes may function as facultative stem cells for each other in conditions of impaired regeneration. The interpretation of the findings derived from these studies has generated considerable discussion and some controversies. This review examines the evidence obtained from the different experimental models and considers implications that these studies may have for human liver disease.
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“Notably, in chronic liver diseases, HHs with expression of progenitor-associated markers were also documented in regenerative nodules (Michalopoulos and Khan, 2015; Yoon et al., 2011”
From In Vitro Expansion of Primary Human Hepatocytes with Efficient Liver Repopulation Capacity (2018) · cites this paper as Michalopoulos and Khan, 2015
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“Cell plasticity has lately been recognized to play an important role in liver regeneration (Kopp et al., 2016; Li et al., 2016; Michalopoulos and Khan, 2015”
From In Vitro Expansion of Primary Human Hepatocytes with Efficient Liver Repopulation Capacity (2018) · cites this paper as Michalopoulos and Khan, 2015
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Song, Y., Lu, Z., Shu, W., Xiang, Z., Wang, Z., Wei, X., & Xu, X. (2023) · Cell Insight · doi:10.1016/j.cellin.2023.100115 · Cited by 2
TGF-β serves as a critical signaling determinant of liver progenitor cell fate and function
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Regulation of essential hepatocyte functions and identity by super-enhancers in health and diseasePreprint
Lin, T., Huang, C., Tong, C., Xu, W., Wang, H., Wu, S., Zhang, W., Li, Y., Liu, H., Shao, C., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.04.657826 · Cited by 2
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The many fates of tissue regeneration
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Metadata
- Authors
- Michalopoulos, G. K., & Khan, Z.
- Affiliations
- University of Pittsburgh (US)
- Venue
- Gastroenterology
- Publisher
- Elsevier BV
- Published
- 2015-10
- Volume
- 149
- Issue
- 4
- Pages
- 876-882
- ISSN
- 0016-5085 (ISSN-L)
- PMC
- PMC4584191
- OpenAlex
- W2112926558
- Cited by
- 109
- References
- 78
- Citations by year
- 2026: 5 · 2025: 4 · 2024: 6 · 2023: 13 · 2022: 10 · 2021: 11 · 2020: 11 · 2019: 10 · 2018: 18 · 2017: 8 · 2016: 10 · 2015: 3
- FWCI
- 1.86
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Gastroenterology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (2r01ca103958-06a1)
- National Cancer Institute (R01CA035373, R01-CA103958)
- National Institute of Diabetes and Digestive and Kidney Diseases (P01DK096990)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (T32HD071834, K12HD052892)
- Topics
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Keywords
- liver stem cells, cholangiocytes, hepatocytes, liver regeneration, liver disease, zebrafish model, rodent models
- MeSH terms
- Animals, Bile Ducts, Intrahepatic, Cell Differentiation, Gene Expression Regulation, Humans, Liver, Liver Diseases, Liver Regeneration, Stem Cells, Signal Transduction, Cell Lineage, Hepatocytes, Cell Proliferation
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