Shackelford R, Adams D O, Johnson S P
Department of Pathology, Duke University Medical Center, Durham, NC 27710.
J Immunol. 1995 Feb 1;154(3):1374-82.
The transcription factor PU.1, the Spi-1 oncogene product, is found principally in B cells and macrophages. PU.1 binds to a purine-rich sequence of DNA with a core consensus sequence of 5'-GAGGAA-3'. By using an electrophoretic mobility shift assay, we have been able to identify PU.1 in nuclear extracts of murine tissue macrophages. When macrophages are stimulated with IFN-gamma, an increase in PU.1 binding is observed. This increase is gradual, peaking at 6 to 9 h and decaying to basal levels 24 h after stimulation. The increase in PU.1 binding is unaffected by inhibiting protein synthesis, but is attenuated by either an inhibitor of the NA+/H+ antiporter or elevations in cAMP. In addition, we have found that low doses (1 ng/ml) of bacterial LPS induce PU.1 binding.
转录因子PU.1是Spi-1癌基因的产物,主要存在于B细胞和巨噬细胞中。PU.1与一段富含嘌呤的DNA序列结合,其核心共有序列为5'-GAGGAA-3'。通过电泳迁移率变动分析,我们已能够在小鼠组织巨噬细胞的核提取物中鉴定出PU.1。当巨噬细胞受到γ干扰素刺激时,观察到PU.1结合增加。这种增加是渐进性的,在刺激后6至9小时达到峰值,并在24小时后衰减至基础水平。PU.1结合的增加不受蛋白质合成抑制的影响,但可被Na+/H+反向转运体抑制剂或cAMP升高所减弱。此外,我们发现低剂量(1 ng/ml)的细菌脂多糖可诱导PU.1结合。