Smith R J, Justen J M, Sam L M
Department of Hypersensitivity Diseases Research, Upjohn Company, Kalamazoo, Michigan 49008.
Inflammation. 1990 Feb;14(1):83-92. doi: 10.1007/BF00914032.
Exposure of human polymorphonuclear neutrophils (PMNs) to recombinant human granulocyte-macrophage colony-stimulating factor (GM-CSF) resulted in a time- and concentration-dependent (3-100 units/ml) extracellular release of a specific (vitamin B12-binding protein) but not azurophil granule constituent (myeloperoxidase). Negligible granule exocytosis occurred if PMNs were not preincubated with cytochalasin B prior to contact with GM-CSF. The extent of degranulation elicited with GM-CSF was reduced but not abolished when PMNs were incubated with EGTA in calcium-free medium. GM-CSF did not stimulate a rise in the cytosolic-free calcium concentration ([Ca2+]i), and it had no effect on PMN protein kinase C (PKC) activity.
将人多形核中性粒细胞(PMN)暴露于重组人粒细胞-巨噬细胞集落刺激因子(GM-CSF)会导致一种特异性物质(维生素B12结合蛋白)呈时间和浓度依赖性(3 - 100单位/毫升)地释放到细胞外,而嗜天青颗粒成分(髓过氧化物酶)则不会。如果PMN在与GM-CSF接触之前未用细胞松弛素B进行预孵育,则颗粒胞吐作用可忽略不计。当PMN在无钙培养基中与乙二醇双四乙酸(EGTA)一起孵育时,GM-CSF引发的脱颗粒程度降低但并未消除。GM-CSF不会刺激胞质游离钙浓度([Ca2+]i)升高,并且对PMN蛋白激酶C(PKC)活性没有影响。