Novel role for EKLF in megakaryocyte lineage commitment

被引:102
作者
Frontelo, Pilar
Manwani, Deepa
Galdass, Mariann
Karsunky, Holger
Lohmann, Felix
Gallagher, Patrick G.
Bieker, James J.
机构
[1] Mt Sinai Sch Med, Brookdale Dept Mol Cell & Dev Biol, New York, NY 10029 USA
[2] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[3] Yale Univ, Sch Med, New Haven, CT USA
关键词
D O I
10.1182/blood-2007-03-082065
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Megakaryocytes and erythroid cells are thought to derive from a common progenitor during hematopoietic differentiation. Although a number of transcriptional regulators are important for this process, they do not explain the bipotential result. We now show by gain- and loss-of-function studies that erythroid Kruppel-like factor (EKLF), a transcription factor whose role in erythroid gene regulation is well established, plays an unexpected directive role in the megakaryocyte lineage. EKLF inhibits the formation of megakaryocytes while at the same time stimulating erythroid differentiation. Quantitative examination of expression during hematopolesis shows that, unlike genes whose presence is required for establishment of both lineages, EKLF is uniquely down-regulated in megakaryocytes after formation of the megakaryocyte-erythroid progenitor. Expression profiling and molecular analyses support these observations and suggest that megakaryocytic inhibition is achieved, at least in part, by EKLF repression of Fli-1 message levels.
引用
收藏
页码:3871 / 3880
页数:10
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