Kulessa H, Frampton J, Graf T
Differentiation Programme, European Molecular Biology Laboratory, Heidelberg, Germany.
Genes Dev. 1995 May 15;9(10):1250-62. doi: 10.1101/gad.9.10.1250.
The transcription factor GATA-1 is expressed in early hematopoietic progenitors and specifically down-regulated in myelomonocytic cells during lineage determination. Our earlier observation that the differentiation of Myb-Ets-transformed chicken hematopoietic progenitors into myeloblasts likewise involves a GATA-1 down-regulation, whereas expression is maintained in erythroid, thrombocytic, and eosinophilic derivatives, prompted us to study the effect of forced GATA-1 expression in Myb-Ets-transformed myeloblasts. We found that the factor rapidly suppresses myelomonocytic markers and induces a reprogramming of myeloblasts into cells resembling either transformed eosinophils or thromboblasts. In addition, we observed a correlation between the level of GATA-1 expression and the phenotype of the cell, intermediate levels of the factor being expressed by eosinophils and high levels by thromboblasts, suggesting a dosage effect of the factor. GATA-1 can also induce the formation of erythroblasts when expressed in a myelomonocytic cell line transformed with a Myb-Ets mutant containing a lesion in Ets. These cells mature into erythrocytes following temperature-inactivation of the Ets protein. Finally, the factor can reprogram a v-Myc-transformed macrophage cell line into myeloblasts, eosinophils, and erythroblasts, showing that the effects of GATA-1 are not limited to Myb-Ets-transformed myeloblasts. Our results suggest that GATA-1 is a lineage-determining transcription factor in transformed hematopoietic cells, which not only activates lineage-specific genetic programs but also suppresses myelomonocytic differentiation. They also point to a high degree of plasticity of transformed hematopoietic cells.
转录因子GATA-1在早期造血祖细胞中表达,并在谱系确定过程中在髓单核细胞中特异性下调。我们早期的观察结果表明,Myb-Ets转化的鸡造血祖细胞向成髓细胞的分化同样涉及GATA-1的下调,而在红系、血小板系和嗜酸性粒细胞衍生物中其表达得以维持,这促使我们研究在Myb-Ets转化的成髓细胞中强制表达GATA-1的效果。我们发现该因子能迅速抑制髓单核细胞标志物,并诱导成髓细胞重编程为类似转化嗜酸性粒细胞或血小板母细胞的细胞。此外,我们观察到GATA-1的表达水平与细胞表型之间存在相关性,嗜酸性粒细胞表达该因子的中间水平,血小板母细胞表达高水平,这表明该因子存在剂量效应。当在由含有Ets损伤的Myb-Ets突变体转化的髓单核细胞系中表达时,GATA-1还能诱导成红细胞的形成。在Ets蛋白经温度失活后,这些细胞成熟为红细胞。最后,该因子能将v-Myc转化的巨噬细胞系重编程为成髓细胞、嗜酸性粒细胞和成红细胞,表明GATA-1的作用不限于Myb-Ets转化的成髓细胞。我们的结果表明,GATA-1是转化造血细胞中的谱系决定转录因子,它不仅激活谱系特异性遗传程序,还抑制髓单核细胞分化。这些结果还表明转化造血细胞具有高度的可塑性。