Helftenbein G, Krusekopf K, Just U, Cross M, Ostertag W, Niemann H, Tamura T
Institut für Virologie, Justus-Liebig Universität Giessen, Germany.
Oncogene. 1996 Feb 15;12(4):931-5.
Differentiation of blood cells is paralleled by a timely ordered expression of cytokine receptor genes. We show here that the expression of the c-fms gene which encodes the lineage-specific receptor for macrophage colony-stimulating factor (M-CSF or CSF-1) is directly linked to ligand-mediated activation of the receptor for the granulocyte/macrophage colony-stimulating factor (GM-CSF). In interleukin-3 (IL-3) dependent multipotent progenitor cells, FDC-Pmix GMV#2 cells, GM-CSF treatment results in the rapid formation of full-length c-fms transcripts. Surprisingly, this upregulation of c-fms transcripts is also observed in mouse NIH3T3 fibroblasts stably transfected with genes coding for the alpha- and beta-subunits of the GM-CSF receptor. These results indicate a direct control by the GM-CSF receptor that takes place regardless of cell differentiation. Furthermore, a 2.1 kb genomic fragment containing the c-fms proximal promoter directs GM-CSF-inducible expression of a reporter gene, suggesting a regulation of c-fms gene expression on the transcriptional level.
血细胞的分化与细胞因子受体基因的适时有序表达并行。我们在此表明,编码巨噬细胞集落刺激因子(M-CSF或CSF-1)谱系特异性受体的c-fms基因的表达与粒细胞/巨噬细胞集落刺激因子(GM-CSF)受体的配体介导激活直接相关。在依赖白细胞介素-3(IL-3)的多能祖细胞FDC-Pmix GMV#2细胞中,GM-CSF处理导致全长c-fms转录本迅速形成。令人惊讶的是,在稳定转染了编码GM-CSF受体α和β亚基基因的小鼠NIH3T3成纤维细胞中也观察到了c-fms转录本的这种上调。这些结果表明GM-CSF受体进行了直接调控,且这种调控与细胞分化无关。此外,一个包含c-fms近端启动子的2.1 kb基因组片段指导报告基因的GM-CSF诱导表达,这表明c-fms基因表达在转录水平上受到调控。