Fukutomi M, Enjoji M, Iguchi H, Yokota M, Iwamoto H, Nakamuta M, Sakai H, Nawata H
Department of Internal Medicine, National Kyushu Cancer Center, Fukuoka, Japan.
Cell Biochem Funct. 2001 Mar;19(1):65-8. doi: 10.1002/cbf.891.
Recent investigations indicate that telomerase activity regulates the life span of cells by compensating for telomere shortening during DNA replication. In addition, as differentiation progresses, telomerase activity is reduced in several different cell lineages. These findings lend support to the theory that more immature cells have greater remaining proliferative capacity and longer life span. However, it has not been directly demonstrated that the differentiation along a hepatocytic or a bile ductal lineage is accompanied by reduction of telomerase activity. In this study, we present direct evidence that telomerase activity is reduced during hepatocytic and biliary epithelial differentiation by using our unique cell lines including a stem-like cell line, ETK-1. When hepatocytic differentiation was induced in ETK-1 by 5-azacytidine, telomerase activity decreased significantly. Similarly, when we compared the telomerase activity on SSP-25 and RBE cell lines from the same origin but representing different maturation stages of cholangiocarcinoma, more mature cells were found to possess significantly lower activity. These results indicate that the generally accepted relationship between telomerase activity and differentiation stage also applies in the hepatocytic and biliary epithelial lineages.
最近的研究表明,端粒酶活性通过补偿DNA复制过程中端粒的缩短来调节细胞寿命。此外,随着分化的进行,几种不同细胞谱系中的端粒酶活性会降低。这些发现支持了这样一种理论,即更不成熟的细胞具有更大的剩余增殖能力和更长的寿命。然而,尚未直接证明沿肝细胞或胆管谱系的分化伴随着端粒酶活性的降低。在本研究中,我们通过使用我们独特的细胞系,包括一种干细胞样细胞系ETK-1,提供了直接证据表明在肝细胞和胆管上皮分化过程中端粒酶活性降低。当用5-氮杂胞苷诱导ETK-1中的肝细胞分化时,端粒酶活性显著降低。同样,当我们比较来自同一来源但代表胆管癌不同成熟阶段的SSP-25和RBE细胞系的端粒酶活性时,发现更成熟的细胞具有显著更低的活性。这些结果表明,端粒酶活性与分化阶段之间普遍接受的关系也适用于肝细胞和胆管上皮谱系。