Suh Hyung Chan, Gooya John, Renn Katie, Friedman Alan D, Johnson Peter F, Keller Jonathan R
Basic Research Program, Science Applications International Corporation-Frederick, National Cancer Institute at Frederick, MD 20702-1201, USA.
Blood. 2006 Jun 1;107(11):4308-16. doi: 10.1182/blood-2005-06-2216. Epub 2006 Feb 9.
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.
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。