Radomska H S, Huettner C S, Zhang P, Cheng T, Scadden D T, Tenen D G
Hematology/Oncology Division, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts, USA.
Mol Cell Biol. 1998 Jul;18(7):4301-14. doi: 10.1128/MCB.18.7.4301.
The transcription factor CCAAT/enhancer binding protein alpha (C/EBPalpha) regulates a number of myeloid cell-specific genes. To delineate the role of C/EBPalpha in human granulopoiesis, we studied its expression and function in human primary cells and bipotential (granulocytic/monocytic) myeloid cell lines. We show that the expression of C/EBPalpha initiates with the commitment of multipotential precursors to the myeloid lineage, is specifically upregulated during granulocytic differentiation, and is rapidly downregulated during the alternative monocytic pathway. Conditional expression of C/EBPalpha alone in stably transfected bipotential cells triggers neutrophilic differentiation, concomitant with upregulation of the granulocyte-specific granulocyte colony-stimulating factor receptor and secondary granule protein genes. Moreover, induced expression of C/EBPalpha in bipotential precursors blocks their monocytic differentiation program. These results indicate that C/EBPalpha serves as a myeloid differentiation switch acting on bipotential precursors and directing them to mature to granulocytes.
转录因子CCAAT/增强子结合蛋白α(C/EBPα)调控许多髓系细胞特异性基因。为了阐明C/EBPα在人类粒细胞生成中的作用,我们研究了其在人类原代细胞和双潜能(粒细胞/单核细胞)髓系细胞系中的表达及功能。我们发现,C/EBPα的表达始于多能前体细胞向髓系谱系的定向分化,在粒细胞分化过程中特异性上调,而在单核细胞分化途径中则迅速下调。在稳定转染的双潜能细胞中单独条件性表达C/EBPα可触发嗜中性粒细胞分化,同时上调粒细胞特异性粒细胞集落刺激因子受体和次级颗粒蛋白基因。此外,在双潜能前体细胞中诱导表达C/EBPα可阻断其单核细胞分化程序。这些结果表明,C/EBPα作为一种髓系分化开关,作用于双潜能前体细胞并引导它们成熟为粒细胞。