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C/EBPα 通过抑制红系分化并诱导髓系分化来决定多能祖细胞中的造血细胞命运。

C/EBPalpha determines hematopoietic cell fate in multipotential progenitor cells by inhibiting erythroid differentiation and inducing myeloid differentiation.

作者信息

Suh Hyung Chan, Gooya John, Renn Katie, Friedman Alan D, Johnson Peter F, Keller Jonathan R

机构信息

Basic Research Program, Science Applications International Corporation-Frederick, National Cancer Institute at Frederick, MD 20702-1201, USA.

出版信息

Blood. 2006 Jun 1;107(11):4308-16. doi: 10.1182/blood-2005-06-2216. Epub 2006 Feb 9.

Abstract

C/EBPalpha is an essential transcription factor required for myeloid differentiation. While C/EBPalpha can act as a cell fate switch to promote granulocyte differentiation in bipotential granulocyte-macrophage progenitors (GMPs), its role in regulating cell fate decisions in more primitive progenitors is not known. We found increased numbers of erythroid progenitors and erythroid cells in C/EBPalpha(-/-) fetal liver (FL). Also, enforced expression of C/EBPalpha in hematopoietic stem cells resulted in a loss of erythroid progenitors and an increase in myeloid cells by inhibition of erythroid development and inducing myeloid differentiation. Conditional expression of C/EBPalpha in murine erythroleukemia (MEL) cells induced myeloid-specific genes, while inhibiting erythroid-specific gene expression including erythropoietin receptor (EpoR), which suggests a novel mechanism to determine hematopoietic cell fate. Thus, C/EBPalpha functions in hematopoietic cell fate decisions by the dual actions of inhibiting erythroid and inducing myeloid gene expression in multipotential progenitors.

摘要

C/EBPα是髓系分化所必需的一种重要转录因子。虽然C/EBPα可作为细胞命运开关,促进双潜能粒细胞-巨噬细胞祖细胞(GMPs)向粒细胞分化,但其在调控更原始祖细胞的细胞命运决定中的作用尚不清楚。我们发现C/EBPα基因敲除小鼠胎肝(FL)中红系祖细胞和红细胞数量增加。此外,在造血干细胞中强制表达C/EBPα会导致红系祖细胞减少,通过抑制红系发育和诱导髓系分化使髓系细胞增加。在小鼠红白血病(MEL)细胞中条件性表达C/EBPα可诱导髓系特异性基因表达,同时抑制包括促红细胞生成素受体(EpoR)在内的红系特异性基因表达,这提示了一种决定造血细胞命运的新机制。因此,C/EBPα通过在多能祖细胞中抑制红系和诱导髓系基因表达的双重作用,在造血细胞命运决定中发挥作用。

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