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在体外胚胎干细胞分化过程中,GATA-1调节终末红系谱系细胞的生长和分化。

GATA-1 regulates growth and differentiation of definitive erythroid lineage cells during in vitro ES cell differentiation.

作者信息

Suwabe N, Takahashi S, Nakano T, Yamamoto M

机构信息

Center for Tsukuba Advanced Research Alliance and Institute of Basic Medical Sciences, University of Tsukuba, Tsukuba, Japan.

出版信息

Blood. 1998 Dec 1;92(11):4108-18.

PMID:9834216
Abstract

Although the importance of GATA-1 in both primitive and definitive hematopoietic lineages has been shown in vivo, the precise roles played by GATA-1 during definitive hematopoiesis have not yet been clarified. In vitro differentiation of embryonic stem (ES) cells using OP9 stroma cells can generate primitive and definitive hematopoietic cells separately, and we have introduced a method that separates hematopoietic progenitors and differentiated cells produced in this system. Closer examination showed that the expression of erythroid transcription factors in this system is regulated in a differentiation stage-specific manner. Therefore, we examined differentiation of GATA-1 promoter-disrupted (GATA-1.05) ES cells using this system. Because the GATA-1.05 mice die by 12.5 embryonic days due to the lack of primitive hematopoiesis, the in vitro analysis is an important approach to elucidate the roles of GATA-1 in definitive hematopoiesis. Consistent with the in vivo observation, differentiation of GATA-1.05 mutant ES cells along both primitive and definitive lineages was arrested in this ES cell culture system. Although the maturation-arrested primitive lineage cells did not express detectable amounts of epsilony-globin mRNA, the blastlike cells accumulated in the definitive stage showed beta-globin mRNA expression at approximately 70% of the wild type. Importantly, the TER119 antigen was expressed and porphyrin was accumulated in the definitive cells, although the levels of both were reduced to approximately 10%, indicating that maturation of definitive erythroid cells is arrested by the lack of GATA-1 with different timing from that of the primitive erythroid cells. We also found that the hematopoietic progenitor fraction of GATA-1.05 cells contains more colony-forming activity, termed CFU-OP9. These results suggest that the GATA-1.05 mutation resulted in proliferation of proerythroblasts in the definitive lineage.

摘要

尽管GATA-1在原始造血谱系和定向造血谱系中的重要性已在体内得到证实,但其在定向造血过程中所起的确切作用尚未阐明。利用OP9基质细胞对胚胎干细胞(ES细胞)进行体外分化,可分别产生原始造血细胞和定向造血细胞,并且我们已经引入了一种方法来分离该系统中产生的造血祖细胞和分化细胞。进一步研究表明,该系统中红系转录因子的表达是以分化阶段特异性的方式进行调控的。因此,我们利用该系统研究了GATA-1启动子缺失(GATA-1.05)的ES细胞的分化情况。由于GATA-1.05小鼠因缺乏原始造血功能在胚胎第12.5天时死亡,因此体外分析是阐明GATA-1在定向造血中作用的重要方法。与体内观察结果一致,在这个ES细胞培养系统中,GATA-1.05突变型ES细胞沿原始和定向谱系的分化均被阻断。尽管成熟受阻的原始谱系细胞未表达可检测量的ε-珠蛋白mRNA,但在定向阶段积累的原始细胞样细胞显示β-珠蛋白mRNA表达水平约为野生型的70%。重要的是,TER119抗原在定向细胞中表达,卟啉在其中积累,尽管两者水平均降至约10%,这表明定向红系细胞的成熟因缺乏GATA-1而受阻,其时间与原始红系细胞不同。我们还发现,GATA-1.05细胞的造血祖细胞部分含有更多的集落形成活性,称为CFU-OP9。这些结果表明,GATA-1.05突变导致定向谱系中早幼红细胞增殖。

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