| Literature DB >> 31938418 |
Yang Tai1, Jin-Hang Gao1,2,3, Chong Zhao2,3, Huan Tong1, Shu-Ping Zheng4, Zhi-Yin Huang1, Rui Liu2,3, Cheng-Wei Tang1,2,3, Jing Li1.
Abstract
SK-Hep1 cells serve as a cell model of hepatocellular carcinoma and hepatocyte biology. However, SK-Hep1 cells are markedly different from normal hepatocytes and other hepatocellular carcinoma cells in their gene expression and protein levels. Furthermore, endothelial-specific makers and morphological characteristics are found in SK-Hep1 cells, indicating an endothelial origin. To confirm their cell phenotype, we investigated and compared the surface ultrastructure, endothelial function, and molecular markers of SK-Hep1 cells in vitro and in vivo. The results revealed that SK-Hep1 cells expressed endothelial-specific makers and exhibited the endothelial function of endocytosis and tubular formation. Capillary-like structures with CD31 expression were also observed in SK-Hep1 allografts in nude mice. Moreover, SK-Hep1 cells possessed fenestrae without diaphragms, consistent with liver sinusoidal endothelial cells, as seen by electron microscopy. In conclusion, SK-Hep1 cells would be better considered a cell model for liver sinusoidal endothelial cells instead of hepatocellular carcinoma cells. IJCEPEntities:
Keywords: Hepatocellular carcinoma; endocytosis; fenestration; liver sinusoidal endothelial cell; tubular formation
Year: 2018 PMID: 31938418 PMCID: PMC6958242
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625