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Adenovirus-mediated hepatocyte nuclear factor-4α overexpression maintains liver phenotype in cultured rat hepatocytes
被引:24
|作者:
Naiki, T
[1
]
Nagaki, M
[1
]
Asano, T
[1
]
Kimata, T
[1
]
Moriwaki, H
[1
]
机构:
[1] Gifu Univ, Grad Sch Med, Dept Gastroenterol, Gifu 5011194, Japan
关键词:
bioartificial liver;
hepatocyte differentiation;
transcription factor;
D O I:
10.1016/j.bbrc.2005.07.102
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Hepatocyte nuclear factor 4 alpha (HNF-4 alpha) is a transcription factor that controls embryonal liver development and that maintains and regulates gene expression in adult liver cells. We have previously demonstrated that transient overexpression of HNF-40 alpha upregulates a number of liver-specific genes in hepatoma cell lines. In this study, we extend these studies by assessing the functional role of HNF-4 alpha in regulating cellular viability and liver-specific functions of primary rat hepatocytes. In cells transfected with an adenovirus vector carrying rat HNF-4 alpha. cDNA, induction and maintenance of liver-specific genes and functions were observed over a long-term culture, which might be associated with the prevention of a rapid loss of the mitochondrial membrane potential. In addition, we demonstrated that transthyretin mRNA was up-regulated by HNF-4 alpha in primary hepatocytes, but not in hepatoma cells. These results indicate that HNF-4a plays a role in the maintenance of morphologically and biochemically functional hepatocytes and that the difference in expression of liver-specific genes induced by HNF-4 alpha may depend on a differentiation state of cells. (c) 2005 Elsevier Inc. All rights reserved.
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页码:496 / 500
页数:5
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