Phagocytosis and inflammatory stimuli induce GM-CSF mRNA in macrophages through posttranscriptional regulation

B Thorens, JJ Mermod, P Vassalli - Cell, 1987 - cell.com
B Thorens, JJ Mermod, P Vassalli
Cell, 1987cell.com
Summary Granulocyte-Macrophage Colony-Stimulating Factor (GM-C%) is a powerful
growth and differentiation factor which acts on hematopoietic progenitor cells and also
activates differentiated granulocytes and macrophages. This study shows that mouse
peritoneal macrophages can be induced to accumulate GM-CSF mRNA and to release GM-
CSF by inflammatory agents (lipopolysaccharide, fetal calf serum, thioglycolate broth);
phagocytosis; and adherence in the presence of fibronectin. GM-CSF mRNA accumulation …
Summary
Granulocyte-Macrophage Colony-Stimulating Factor (GM-C%) is a powerful growth and differentiation factor which acts on hematopoietic progenitor cells and also activates differentiated granulocytes and macrophages. This study shows that mouse peritoneal macrophages can be induced to accumulate GM-CSF mRNA and to release GM-CSF by inflammatory agents (lipopolysaccharide, fetal calf serum, thioglycolate broth); phagocytosis; and adherence in the presence of fibronectin. GM-CSF mRNA accumulation, which is totally prevented by the corticosteroid dexamethasone and by interferon-y, is not accompanied by changes in the gene’s transcriptional level. No interleukin 3 (multi-CSF) mRNA is detectable in induced macrophages. These findings have implications in the understanding of hematopoiesis and of the inflammation and repair process.
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