Generation of a primitive erythroid cell line and promotion of its growth by basic fibroblast growth factor

被引:16
作者
Yuen, D
Mittal, L
Deng, CX
Choi, KH
机构
[1] Univ Maryland, Dept Pathol, Program Mol & Cell Biol, Baltimore, MD 21201 USA
[2] NIDDKD, Biochem & Metab Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1182/blood.V91.9.3202.3202_3202_3209
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
An immortalized cell line representing the primitive erythroid (EryP) lineage was established from in vitro-differentiated progeny (embryoid bodies [EBs]) of embryonic stem (ES) cells using a retroviral insertional mutation, and has been termed EB-PE for embryoid body-derived primitive erythroid. Even though EB-PE cells are immortalized, they show characteristics of normal EryP cells, such as gene expression and growth factor dependency. In addition, EB-PE cells can differentiate further in culture. Investigation of growth factor requirements of EB-PE cells showed that basic fibroblast growth factor (bFGF) and erythropoietin (Epo) play unique roles in EB-PE proliferation and differentiation. While bFGF was a strong mitogen, Epo was required for both proliferation and differentiation. The unique proliferative response to bFGF coincided with upregulation of its receptor, fibroblast growth factor receptor (fgfr-1), and downregulation of erythropoietin receptor (EpoR) gene expression. Studies of primary EryP cells derived from early EBs, when tested in a colony formation assay, also provided evidence for the mitogenic role of bFGF in concert with Epo, (C) 1998 by The American Society of Hematology.
引用
收藏
页码:3202 / 3209
页数:8
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