Thorens B, Mermod J J, Vassalli P
Cell. 1987 Feb 27;48(4):671-9. doi: 10.1016/0092-8674(87)90245-5.
Granulocyte-Macrophage Colony-Stimulating Factor (GM-CSF) 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-gamma, 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.
粒细胞-巨噬细胞集落刺激因子(GM-CSF)是一种强大的生长和分化因子,作用于造血祖细胞,还能激活分化的粒细胞和巨噬细胞。本研究表明,炎性因子(脂多糖、胎牛血清、巯基乙酸盐肉汤)、吞噬作用以及在纤连蛋白存在下的黏附作用可诱导小鼠腹腔巨噬细胞积累GM-CSF mRNA并释放GM-CSF。GM-CSF mRNA的积累完全被皮质类固醇地塞米松和干扰素-γ所抑制,且其基因转录水平未发生变化。在诱导的巨噬细胞中未检测到白细胞介素3(多集落刺激因子)mRNA。这些发现对于理解造血作用以及炎症和修复过程具有重要意义。