Späth G F, Weiss M C
Unité de Génétique de la Différenciation, URA 1149, Centre National de la Recherche Scientifique, Institut Pasteur, Paris, France.
Mol Cell Biol. 1997 Apr;17(4):1913-22. doi: 10.1128/MCB.17.4.1913.
The capacity of the liver-enriched transcription factor hepatocyte nuclear factor 4 (HNF4) to direct redifferentiation of dedifferentiated rat hepatoma cells was investigated by stable transfection of epitope-tagged HNF4 cDNA into H5 variant cells. HNF4-producing cells expressed the previously silent HNF1 gene and showed activation of some hepatic functions, including alpha1-antitrypsin, beta-fibrinogen, and transthyretin, but not of the endogenous HNF4 gene. Expression of the other hepatocyte-enriched transcription factors was not modified. Treatment of the HNF4tag-expressing cells with dexamethasone induced expression of the transgene by 10-fold, resulting in enhanced expression of target genes of both glucocorticoid hormones and HNF4. The set of activated hepatic genes was extended by treatment of cells with the demethylating agent 5-azacytidine followed by selection in dexamethasone-containing glucose-free medium. Some of the colonies that developed reexpressed the entire set of hepatic functions tested. Fusion of HNF4tag-producing H5 cells with well-differentiated Fao cells showed that only those hybrids which maintained expression of HNF4tag were protected from complete extinction, including that of the Fao HNF4 gene. Thus, H5 cells must produce an extinguisher of the HNF4 gene. In addition, this result implies that HNF4 itself, or its target HNF1, is a positive regulator of HNF4. In conclusion, HNF4tag expression overcomes repression of the hepatic phenotype of the H5 cell without abolishing its potential to extinguish an active genome. Taken together, these results predict that expression of HNF4 should be sufficient to establish heritable expression of many parameters of the hepatic differentiated state.
通过将表位标记的HNF4 cDNA稳定转染到H5变异细胞中,研究了肝脏富集转录因子肝细胞核因子4(HNF4)指导去分化大鼠肝癌细胞再分化的能力。产生HNF4的细胞表达了之前沉默的HNF1基因,并显示出一些肝功能的激活,包括α1-抗胰蛋白酶、β-纤维蛋白原和甲状腺素运载蛋白,但内源性HNF4基因未被激活。其他肝脏富集转录因子的表达未发生改变。用地塞米松处理表达HNF4标签的细胞可使转基因表达增加10倍,导致糖皮质激素和HNF4的靶基因表达增强。用去甲基化剂5-氮杂胞苷处理细胞,随后在含地塞米松的无葡萄糖培养基中进行筛选,可扩展激活的肝脏基因集。形成的一些集落重新表达了所测试的全套肝功能。将产生HNF4标签的H5细胞与分化良好的Fao细胞融合,结果表明只有那些维持HNF4标签表达的杂种细胞才能避免完全灭绝,包括Fao HNF4基因的灭绝。因此,H5细胞必定产生了一种HNF4基因的抑制因子。此外,这一结果意味着HNF4本身或其靶标HNF1是HNF4的正向调节因子。总之,HNF4标签的表达克服了H5细胞肝表型的抑制,同时又没有消除其使活跃基因组沉默的潜力。综上所述,这些结果预示HNF4的表达应该足以建立肝脏分化状态许多参数的可遗传表达。