Magee D M, Wing E J, Ampel N M, Waheed A, Shadduck R K
Department of Medicine, Montefiore Hospital, University of Pittsburgh School of Medicine, PA 15213.
Immunology. 1987 Nov;62(3):373-8.
Experiments were performed to test the postulate that macrophage colony-stimulating factor (M-CSF) modulates the expression of specific membrane structures on mature murine macrophages. Resident peritoneal macrophages were incubated with M-CSF for 48-72 hr and analysed for Fc receptor and Ia antigen expression. M-CSF treatment of macrophages increased the expression of Fc receptors two- to three-fold over that of unstimulated macrophages. The effect was detected at 1 U/ml of M-CSF, with maximal expression between 100 and 500 U/ml. The specificity of the enhancement was indicated by two sets of experiments. Purified rabbit anti-M-CSF IgG, but not normal rabbit IgG, inhibited the M-CSF-mediated Fc receptor enhancement. Also, a highly purified M-CSF preparation, which was essentially free of endotoxin and interferon, was active in these assays. M-CSF augmented both major types of IgG Fc receptors, FcR I (recognizing IgG 2a) and FcR II (recognizing IgG 2b/IgG1). A second membrane marker, the Ia antigen, was induced by recombinant IFN-gamma (rIFN-gamma) but not by M-CSF. These results indicate that M-CSF is an inducer of two classes of IgG Fc receptors on mature tissue macrophages.
进行实验以检验巨噬细胞集落刺激因子(M-CSF)调节成熟小鼠巨噬细胞上特定膜结构表达的假设。将驻留腹膜巨噬细胞与M-CSF孵育48 - 72小时,并分析其Fc受体和Ia抗原表达。用M-CSF处理巨噬细胞后,其Fc受体的表达比未刺激的巨噬细胞增加了两到三倍。在1 U/ml的M-CSF时可检测到这种效应,在100至500 U/ml之间表达达到最大值。两组实验表明了这种增强作用的特异性。纯化的兔抗M-CSF IgG可抑制M-CSF介导的Fc受体增强,而正常兔IgG则无此作用。此外,一种高度纯化的M-CSF制剂,基本不含内毒素和干扰素,在这些实验中具有活性。M-CSF增强了两种主要类型的IgG Fc受体,即FcR I(识别IgG 2a)和FcR II(识别IgG 2b/IgG1)。第二种膜标记物Ia抗原由重组干扰素-γ(rIFN-γ)诱导,但不由M-CSF诱导。这些结果表明,M-CSF是成熟组织巨噬细胞上两类IgG Fc受体的诱导剂。