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

被引:4
作者
Shimizu, Takahisa [1 ]
Esaki, Lisa [1 ]
Mizuno, Hiroko [1 ]
Takeda, Ken [1 ]
机构
[1] Tokyo Univ Sci, Fac Pharmaceut Sci, Dept Hyg Chem, Noda, Chiba 2788510, Japan
关键词
leukemia; differentiation; retinoic acid; GM-CSF; cDNA microarray; LEUKEMIA ML-1 CELLS; ACUTE PROMYELOCYTIC LEUKEMIA; PROTEIN-KINASE-C; GM-CSF; MESSENGER-RNA; THYROID-HORMONE; HL-60; CELLS; DIFFERENTIATION; INDUCTION; NEUTROPHILS;
D O I
10.1189/jlb.0905502
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 Northen 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.
引用
收藏
页码:889 / 896
页数:8
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