Krishnaraju K, Nguyen H Q, Liebermann D A, Hoffman B
Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
Mol Cell Biol. 1995 Oct;15(10):5499-507. doi: 10.1128/MCB.15.10.5499.
Previously we have shown that the zinc finger transcription factor Egr-1 is essential for and restricts differentiation of hematopoietic cells along the macrophage lineage, raising the possibility that Egr-1 actually plays a deterministic role in governing the development of hematopoietic precursor cells along the monocytic lineage. To test this hypothesis, we have taken advantage of interleukin-3-dependent 32Dcl3 hematopoietic precursor cells which, in addition to undergoing granulocytic differentiation in response to granulocyte colony-stimulating factor, were found to be induced for limited proliferation, but not differentiation, by granulocyte-macrophage colony-stimulating factor. It was shown that ectopic expression of Egr-1 blocked granulocyte colony-stimulating factor-induced terminal granulocytic differentiation, consistent with previous findings. In addition, ectopic expression of Egr-1 endowed 32Dcl3 cells with ability to be induced by granulocyte-macrophage colony-stimulating factor for terminal differentiation exclusively along the macrophage lineage. Thus, evidence that Egr-1 potentiates terminal macrophage differentiation has been obtained, suggesting that Egr-1 plays a deterministic role in governing the development of hematopoietic cells along the macrophage lineage.
此前我们已经表明,锌指转录因子Egr-1对造血细胞沿巨噬细胞谱系的分化至关重要且具有限制作用,这增加了Egr-1实际上在控制造血前体细胞沿单核细胞谱系发育中起决定性作用的可能性。为了验证这一假设,我们利用了依赖白细胞介素-3的32Dcl3造血前体细胞,这些细胞除了在粒细胞集落刺激因子的作用下进行粒细胞分化外,还被发现可被粒细胞-巨噬细胞集落刺激因子诱导进行有限的增殖,但不会分化。结果表明,Egr-1的异位表达阻断了粒细胞集落刺激因子诱导的终末粒细胞分化,这与之前的研究结果一致。此外,Egr-1的异位表达使32Dcl3细胞具有被粒细胞-巨噬细胞集落刺激因子诱导仅沿巨噬细胞谱系进行终末分化的能力。因此,已经获得了Egr-1增强终末巨噬细胞分化的证据,表明Egr-1在控制造血细胞沿巨噬细胞谱系发育中起决定性作用。