MECHANISMS OF DIFFERENTIATION OF U937-LEUKEMIC CELLS INDUCED BY GM-CSF AND 1,25(OH)2 VITAMIN-D3

被引:34
作者
KIM, YR
ABRAHAM, NG
LUTTON, JD
机构
[1] NEW YORK MED COLL,DEPT CELL BIOL & ANAT,VALHALLA,NY 10595
[2] NEW YORK MED COLL,DEPT MED,VALHALLA,NY 10595
关键词
U937; GM-CSF; 1,25(OH)2VITAMIN-D3; C-MYC; C-FOS; CELL CYCLE; MONOCYTE-ANTIGENS; DIFFERENTIATION;
D O I
10.1016/0145-2126(91)90050-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The human monoblast cell line, U937, was employed to elucidate early events associated with differentiation induced by granulocyte-macrophage colony-stimulating factor (GM-CSF) and 1,25-dihydroxy-Vitamin D3 (VD3). Exposure of cells to a combination of GM-CSF and VD3 resulted in an up-regulation of c-fos mRNA within 1 h and a marked down-regulation of c-myc mRNA by 24 h and this was associated with a shift of cell population from the S phase to the G0 + G1 phase of the cell cycle by 18%. This was followed by a marked enhancement of monocyte-associated cell surface antigens [OKM1 (CD11b), LeuM3 (CD14), M77.7], as determined by monoclonal antibodies and flow cytometry. Functional characteristics such as nitrobule-tetrazolium reduction, alpha-naphthyl butyrate esterase activity, and phagocytic capability occurred. Cells treated with GM-CSF or VD3 alone showed only minor changes. These results demonstrate a potent synergistic effect of GM-CSF and VD3 on induction of U937 differentiation. This differentiation was partially blocked by H7, a protein kinase C (PKC) inhibitor. Changes in c-myc and c-fos mRNA expressions and a shift in cell cycle were shown to be early events in this process.
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页码:409 / &
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