Kim Jynho, Ogata Yoshiyasu, Ali Humayra, Feldman Ricardo A
Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Blood Cells Mol Dis. 2004 Mar-Apr;32(2):302-8. doi: 10.1016/j.bcmd.2003.12.004.
The c-fps/fes protooncogene encodes a 92-kDa protein tyrosine kinase that is involved in myeloid cell development and immune responses of granulocytes and macrophages. To help define its biological role and mechanism of action, we have developed a gain of function allele of Fes that has potent biological activity in myeloid cells. Introduction of constitutively active Fes into myeloid progenitors induced the appearance of fully differentiated macrophages or granulocytes depending on the lineage commitment of the transduced cells. We found that Fes-induced macrophage differentiation correlated with activation of the ets family transcription factor PU.1, which is essential for macrophage development. On the other hand, granulocyte differentiation by Fes was mediated through activation of CCAAT/enhancer-binding protein alpha (C/EBP-alpha) and STAT3, two transcription factors that are critical for granulocytic differentiation. We postulate that Fes transduces inductive signals for terminal macrophage and granulocyte differentiation, and that this biological activity is mediated through the activation of lineage-specific transcription factors.
原癌基因c-fps/fes编码一种92 kDa的蛋白酪氨酸激酶,它参与髓样细胞发育以及粒细胞和巨噬细胞的免疫反应。为了帮助确定其生物学作用和作用机制,我们构建了一个Fes功能获得性等位基因,该等位基因在髓样细胞中具有强大的生物学活性。将组成型激活的Fes导入髓样祖细胞会诱导完全分化的巨噬细胞或粒细胞出现,这取决于转导细胞的谱系定向。我们发现Fes诱导的巨噬细胞分化与ets家族转录因子PU.1的激活相关,PU.1对巨噬细胞发育至关重要。另一方面,Fes诱导的粒细胞分化是通过CCAAT/增强子结合蛋白α(C/EBP-α)和STAT3的激活介导的,这两个转录因子对粒细胞分化至关重要。我们推测Fes转导终末巨噬细胞和粒细胞分化的诱导信号,并且这种生物学活性是通过谱系特异性转录因子的激活介导的。