Lehtonen Anne, Matikainen Sampsa, Miettinen Minja, Julkunen Ilkka
Laboratory of Viral and Molecular Immunology, Department of Microbiology, National Public Health Institute, Mannerheimintie 166, FIN-0300 Helsinki, Finland.
J Leukoc Biol. 2002 Mar;71(3):511-9.
GM-CSF signals through JAK2 and STAT5 and stimulates the expression of STAT5 target genes, such as pim-1 and CIS. Analyzed by EMSA, GM-CSF stimulation led to much stronger STAT5 DNA-binding to pim-1 or CIS GAS elements in primary human monocytes compared with mature macrophages. Similarly, GM-CSF-induced expression of pim-1 and CIS mRNAs was much stronger in monocytes. These differencies were not a result of downregulation of the GM-CSF receptor system or STAT5 expression, because monocytes and macrophages readily expressed GM-CSF receptor, JAK2, STAT5A, and STAT5B mRNAs and proteins. Monocytes expressed significant amounts of truncated STAT5 forms that took part in STAT5-DNA complex formation in GM-CSF-stimulated monocytes. This resulted in faster moving STAT5 complexes compared with macrophages in EMSA. Our results demonstrate that STAT5 isoform expression, GM-CSF-induced STAT5 activation, and STAT5 target-gene expression are altered significantly during monocyte/macrophage differentiation.
粒细胞-巨噬细胞集落刺激因子(GM-CSF)通过JAK2和STAT5发出信号,并刺激STAT5靶基因的表达,如pim-1和CIS。通过电泳迁移率变动分析(EMSA)检测,与成熟巨噬细胞相比,GM-CSF刺激导致原代人单核细胞中STAT5与pim-1或CIS的γ干扰素激活位点(GAS)元件的DNA结合能力更强。同样,GM-CSF诱导的pim-1和CIS mRNA表达在单核细胞中也更强。这些差异并非GM-CSF受体系统或STAT5表达下调所致,因为单核细胞和巨噬细胞均能轻易表达GM-CSF受体、JAK2、STAT5A和STAT5B的mRNA及蛋白质。单核细胞表达大量截短的STAT5形式,其参与GM-CSF刺激的单核细胞中STAT5-DNA复合物的形成。这导致在EMSA中与巨噬细胞相比,STAT5复合物迁移更快。我们的结果表明,在单核细胞/巨噬细胞分化过程中,STAT5异构体表达、GM-CSF诱导的STAT5激活及STAT5靶基因表达均发生显著改变。