ArticleThe American journal of pathology2000
The in vitro differentiating capacity of nonparenchymal epithelial cells derived from adult porcine livers.
Article in The American journal of pathology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 29 citations in OpenAlex.
- "Small Hepatocytes" in the Liver.Cells · 2023Review
- Side Population Cells From an Immortalized Human Liver Epithelial Cell Line Exhibit Hepatic Stem-Like Cell Properties.Cell medicine · 2012Article
- Activation, isolation, identification and culture of hepatic stem cells from porcine liver tissues.Cell proliferation · 2011Article
- Culture of newborn monkey liver epithelial progenitor cells in chemical defined serum-free medium.In vitro cellular & developmental biology. Animal · 2010Article
- Hepatic reconstruction from fetal porcine liver cells using a radial flow bioreactor.World journal of gastroenterology · 2008Article
- Epithelial cells with hepatobiliary phenotype: is it another stem cell candidate for healthy adult human liver?World journal of gastroenterology · 2007Article
- Hepatic stem cells: from inside and outside the liver?Cell proliferation · 2004Review
- Presence of side-population cells in an immortalized nontumorigenic human liver epithelial cell line.In vitro cellular & developmental biology. AnimalArticle
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Specific nonparenchymal epithelial cell (NPEC) clusters derived from normal adult porcine livers demonstrate a characteristic developmental pattern in the presence of other types of nonparenchymal cells in vitro. This pattern includes scattering, colonial growth, and an emergence of duct-like structures (DLSs) in the colonies. It has been confirmed that 96% of the scattered cell clusters in these cultures develop into colonies containing DLSs. In this study, we examine the differentiation of NPEC clusters using the scattered formation as a marker of the DLS-emerged colonies. We report that the NPECs expressed albumin, alpha-fetoprotein, transferrin, cytokeratin (CK) 18, CK7, and c-met, but not alpha-1-antitrypsin (AAT), at the scattering stage. In addition, at the same stage, NPECs expressed oval-cell-related markers such as OV6, but not biliary epithelial cell (BEC) markers such as gamma-glutamyltransferase, CK19, and CK14. At the DLS emerging stage, hepatocyte markers, including AAT, were detectable in the cells either at the periphery of colonies or in the cells surrounded by the DLSs. On the other hand, the cells constituting DLSs expressed BEC markers, suggesting a bile duct nature of the DLSs. Furthermore, the cells in the colonies possessed an ultrastructural appearance of differentiated hepatocytes and BECs. These results suggest that certain NPECs are bipotent, and that, in culture, they mimic hepatoblast development in vivo.
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