In vitro development of erythroid and megakaryocytic cells from a UT-7 subline, UT-7/GM

被引:37
作者
Komatsu, N [1 ]
Kirito, K [1 ]
Shimizu, R [1 ]
Kunitama, M [1 ]
Yamada, M [1 ]
Uchida, M [1 ]
Takatoku, M [1 ]
Eguchi, M [1 ]
Miura, Y [1 ]
机构
[1] DOKKYO MED SCH,DEPT PEDIAT 2,MIBU,TOCHIGI,JAPAN
关键词
D O I
10.1182/blood.V89.11.4021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
UT-7 is a human megakaryoblastic leukemia cell line with absolute dependence on interleukin-3, granulocyte-macrophage colony-stimulating factor (GM-CSF), or erythropoietin (EPO) for growth and survival. We isolated a novel subline, UT-7/GM after long-term culture of UT-7 with GM-CSF. The hemoglobin concentration and gamma-globin and EPO-receptor mRNA levels were significantly higher in EPO-treated UT-7/GM cells than in untreated cells. In contrast, the platelet factor 4 and glycoprotein IIb mRNA levels were much higher in thrombopoietin (TPO)-treated UT-7/GM cells than in untreated cells, Some TPO-treated cells had morphologically mature megakaryocytic characteristics such as a developed demarcation membrane in the cytoplasm and multilobular nuclei. These findings indicate that UT-7/GM is a bipotential cell line that can be induced to differentiate into erythroid and megakaryocytic lineages by EPO and TPO, respectively, Moreover, a minority of UT-7/GM cells acquired a high hemoglobin concentration by treatment with TPO, suggesting that TPO in part induced the erythroid differentiation of the UT-7/GM cells. Interestingly, GM-CSF inhibited the EPO- or TPO-induced erythroid differentiation and the TPO-induced megakaryocytic differentiation of UT-7/GM cells. These results support the hypothesis that cytokines influence the programming of gene expression required for lineage commitment or differentiation. (C) 1997 by The American Society of Hematology.
引用
收藏
页码:4021 / 4033
页数:13
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