STUDIES ON THE MECHANISM OF PLATELET-ACTIVATING FACTOR PRODUCTION IN GM-CSF PRIMED NEUTROPHILS - INVOLVEMENT OF PROTEIN-SYNTHESIS AND PHOSPHOLIPASE-A2 ACTIVATION

被引:19
作者
WIRTHMUELLER, U
DEWECK, AL
DAHINDEN, CA
机构
[1] Institute of Clinical Immunology, Inselspital
关键词
D O I
10.1016/0006-291X(90)92127-L
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
GM-CSF regulates the growth of hemopoietic progenitor cells, enhances the responsiveness of mature PMN and primes these cells for synthesis of leukotrienes and PAF in response to secondary stimuli. The biochemical requirements for PAF production in GM-CSF primed PMN was examined using different metabolic inhibitors. GM-CSF stimulates uridine incorporation into RNA and inhibitors for RNA and protein synthesis decrease PAF synthesis in our model. This suggests a role for gene expression and de novo synthesis of proteins in the action of GM-CSF. Different PLA2 inhibitors, including a 9 amino-acid peptide derived from a conserved region of hte calpactin superfamily, decrease PAF production, indicating that in GM-CSF primed PMN the chemotactic peptide fMLP triggers lipid mediator synthesis by activating PLA2. © 1990.
引用
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页码:556 / 562
页数:7
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