外胚层
同源盒蛋白纳米
生物
白血病抑制因子
雷克斯1
纳米同源盒蛋白
内细胞团
胚胎干细胞
细胞生物学
诱导多能干细胞
内胚层
干细胞
SOX2
重编程
胚状体
细胞分化
胚泡
转录因子
遗传学
原肠化
胚胎
胚胎发生
基因
作者
Kiyofumi Mitsui,Yoshimi Tokuzawa,Hiroaki Itoh,Kohichi Segawa,Masanaka Murakami,Kazutoshi Takahashi,Masayoshi Maruyama,Masayuki Maeda,Shinya Yamanaka
出处
期刊:Cell
[Elsevier]
日期:2003-05-01
卷期号:113 (5): 631-642
被引量:2990
标识
DOI:10.1016/s0092-8674(03)00393-3
摘要
Embryonic stem (ES) cells derived from the inner cell mass (ICM) of blastocysts grow infinitely while maintaining pluripotency. Leukemia inhibitory factor (LIF) can maintain self-renewal of mouse ES cells through activation of Stat3. However, LIF/Stat3 is dispensable for maintenance of ICM and human ES cells, suggesting that the pathway is not fundamental for pluripotency. In search of a critical factor(s) that underlies pluripotency in both ICM and ES cells, we performed in silico differential display and identified several genes specifically expressed in mouse ES cells and preimplantation embryos. We found that one of them, encoding the homeoprotein Nanog, was capable of maintaining ES cell self-renewal independently of LIF/Stat3. nanog-deficient ICM failed to generate epiblast and only produced parietal endoderm-like cells. nanog-deficient ES cells lost pluripotency and differentiated into extraembryonic endoderm lineage. These data demonstrate that Nanog is a critical factor underlying pluripotency in both ICM and ES cells.
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