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Nanog蛋白在小鼠F9胚胎癌细胞及其内胚层分化对应细胞中的作用。

Roles of the Nanog protein in murine F9 embryonal carcinoma cells and their endoderm-differentiated counterparts.

作者信息

Chen Yanmei, Du Zhongwei, Yao Zhen

机构信息

Laboratory of Molecular and Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, Shanghai 200031, China.

出版信息

Cell Res. 2006 Jul;16(7):641-50. doi: 10.1038/sj.cr.7310067.

Abstract

Nanog is a recently discovered homeodomain transcription factor that sustains the pluripotency of embryonic stem (ES) cells and blocks their differentiation into endoderm. The murine F9 embryonal carcinoma cell line is a well-documented model system for endoderm cell lineage differentiation. Here, we examined the function of Nanog in F9 cell endoderm differentiation. Over-expression of Nanog returns the F9 cells to the early status of ES cells and represses the differentiation of primitive endoderm and parietal endoderm in F9 cells, whereas it has no effect on the differentiation of visceral endoderm. In contrast, the expression of C-terminal domain-truncated Nanog spontaneously promotes endoderm differentiation in F9 cells. These data suggest that Nanog is required to sustain the proper undifferentiated status of F9 cells, and the C-terminal domain of Nanog transduces the most effects in repressing primitive endoderm and parietal endoderm differentiation in F9 cells.

摘要

Nanog是最近发现的一种同源结构域转录因子,它维持胚胎干细胞(ES细胞)的多能性,并阻止其向内胚层分化。小鼠F9胚胎癌细胞系是内胚层细胞谱系分化的一个有充分文献记载的模型系统。在此,我们研究了Nanog在F9细胞内胚层分化中的功能。Nanog的过表达使F9细胞恢复到ES细胞的早期状态,并抑制F9细胞中原始内胚层和壁内胚层的分化,而对内胚层的分化没有影响。相反,C末端结构域截短的Nanog的表达在F9细胞中自发促进内胚层分化。这些数据表明,Nanog是维持F9细胞适当未分化状态所必需的,并且Nanog的C末端结构域在抑制F9细胞中原始内胚层和壁内胚层分化方面发挥了最大作用。

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