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粒细胞巨噬细胞集落刺激因子增强视黄酸诱导的基因表达。

Granulocyte macrophage colony-stimulating factor enhances retinoic acid-induced gene expression.

作者信息

Shimizu Takahisa, Esaki Lisa, Mizuno Hiroko, Takeda Ken

机构信息

Department of Hygiene-Chemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba 278-8510, Japan.

出版信息

J Leukoc Biol. 2006 Oct;80(4):889-96. doi: 10.1189/jlb.0905502. Epub 2006 Aug 2.

Abstract

We reported previously that treatment of human myeloblastic leukemia ML-1 cells with all-trans retinoic acid (ATRA) in combination with GM-CSF enhances the granulocytic differentiation, which is induced only slightly by ATRA alone. To investigate the mechanism underlying this differentiation and the synergistic effect of ATRA and GM-CSF, we used cDNA microarray to examine gene expression profiles of ML-1 cells treated with ATRA and/or GM-CSF. We identified 22 up-regulated genes in ML-1 cells treated with both reagents and examined the expression of these genes in cells treated with ATRA and/or GM-CSF by Northern blot analysis. Comparison of cells treated with both reagents and cells treated with ATRA or GM-CSF alone revealed that expression of nine of the 19 genes was induced synergistically by combined treatment with ATRA and GM-CSF. Expression of most of these genes was increased only slightly by ATRA alone, and this induction was enhanced by the addition of GM-CSF. These results indicate that GM-CSF enhances ATRA-induced gene expression. Moreover, studies with inhibitors of signaling molecules suggested that activation of JAK2 is associated with the synergistic induction of several genes by ATRA and GM-CSF. JAK2 inhibitor suppressed induction of NBT-reducing activity in ML-1 cells treated with both reagents. It is likely that the enhancer effect of GM-CSF on ATRA-induced gene expression leads to the differentiation induced synergistically by ATRA combined with GM-CSF. Further studies of the mechanism underlying this effect may identify better approaches for the treatment of RA-insensitive leukemia.

摘要

我们先前报道,用全反式维甲酸(ATRA)联合粒细胞-巨噬细胞集落刺激因子(GM-CSF)处理人髓母细胞白血病ML-1细胞,可增强粒细胞分化,而单独使用ATRA时这种分化诱导作用微弱。为研究这种分化的潜在机制以及ATRA与GM-CSF的协同作用,我们使用cDNA微阵列检测经ATRA和/或GM-CSF处理的ML-1细胞的基因表达谱。我们鉴定出在用两种试剂处理的ML-1细胞中有22个上调基因,并通过Northern印迹分析检测了这些基因在经ATRA和/或GM-CSF处理的细胞中的表达。比较用两种试剂处理的细胞与单独用ATRA或GM-CSF处理的细胞发现,19个基因中的9个基因的表达在ATRA与GM-CSF联合处理时被协同诱导。这些基因中的大多数仅在单独使用ATRA时略有增加,而加入GM-CSF可增强这种诱导作用。这些结果表明GM-CSF增强了ATRA诱导的基因表达。此外,对信号分子抑制剂的研究表明,JAK2的激活与ATRA和GM-CSF对几个基因的协同诱导有关。JAK2抑制剂抑制了在用两种试剂处理的ML-1细胞中NBT还原活性的诱导。GM-CSF对ATRA诱导的基因表达的增强作用可能导致ATRA与GM-CSF联合协同诱导的分化。对这种作用潜在机制的进一步研究可能会找到治疗对RA不敏感白血病的更好方法。

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