THE EFFECTS OF GM-CSF ON MYELOPEROXIDASE RELEASE IN NORMAL AND MYELODYSPLASTIC NEUTROPHILS

被引:11
作者
DANG, Y
LOWE, GM
EDWARDS, SW
GALVANI, DW
机构
[1] ROYAL LIVERPOOL UNIV,TEACHING HOSP,DEPT HAEMATOL,POB 147,LIVERPOOL L69 3BX,ENGLAND
[2] ROYAL LIVERPOOL UNIV,TEACHING HOSP,DEPT BIOCHEM,LIVERPOOL L69 3BX,ENGLAND
关键词
GM-CSF; MYELOPEROXIDASE; MYELODYSPLASTIC NEUTROPHILS;
D O I
10.1016/0145-2126(93)90160-M
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
When purified control neutrophils were primed with GM-CSF, a significant increase in FMLP-induced MPO release was observed (mean +/- S.E.M., 3.4 +/- 0.8 mU/10(7) unprimed cells compared to 6.5 +/- 1.1 mU/10(7) primed cells, p < 0.001). This MPO release was greatly augmented by Cytochalasin B (Cy B), but after the addition of Cy B the priming effects of GM-CSF became less obvious. Exposure to GM-CSF without FMLP did not enhance MPO release. Within whole blood, FMLP produced negligible MPO release, but priming with GM-CSF prior to FMLP always resulted in a significant increase in MPO release. Myelodysplastic neutrophils released similar amounts of MPO in response to FMLP, compared with control cells (3.4 +/- 0.8 mU/10(7) control cells compared to 2.7 +/- 0.3 mU/10(7) MDS cells, p > 0.05). Priming with GM-CSF produced an increase in FMLP-stimulated MPO release comparable with control cells. In terms of total MPO content, although some MDS patients exhibited low levels, as a group there was no significant difference from controls (169 +/- 21 MU/10(7) control cells compared with 157 +/- 19 mU/10(7) MDS cells). These findings suggest that MPO activity is not a universal defect in MDS and cannot account for the defects in respiratory burst activity in these neutrophils.
引用
收藏
页码:1037 / 1044
页数:8
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