Liesveld J L, Abboud C N, Looney R J, Ryan D H, Brennan J K
Department of Medicine, University of Rochester School of Medicine and Dentistry, NY 14642.
J Immunol. 1988 Mar 1;140(5):1527-33.
Three classes of FcR have been defined on human myeloid cells by their reactivity with mAb; FcRI (mAb 32); FcRII (mAb IV3); and FcRIII (mAb 3G8). We have quantitated the expression of each FcR on human myeloid leukemia cells and cell lines (KG-1, HL-60, U937, and K562). Detailed analysis of FcR surface expression is provided for the U937 cell line after exposure to CSF and cytokines. Increased expression of FcRI and FcRII occurred at 72 h in cells exposed to GCT or Mo cell line-conditioned medium as well as to medium from PHA-treated mononuclear cells. The augmentation of FcRII required protein synthesis and was diminished by a neutralizing antibody to granulocyte-macrophage CSF. We also show that fractions containing natural granulocyte CSF or granulocyte-macrophage CSF as well as r-granulocyte and r-granulocyte-macrophage CSF are capable of inducing FcRII on these cells, whereas other cytokines such as IL-1 and IL-2, TNF-alpha, INF-gamma and macrophages CSF failed to do so.
根据与单克隆抗体的反应性,已在人髓细胞上定义了三类FcR;FcRI(单克隆抗体32);FcRII(单克隆抗体IV3);和FcRIII(单克隆抗体3G8)。我们已经对人髓性白血病细胞和细胞系(KG-1、HL-60、U937和K562)上每种FcR的表达进行了定量。在U937细胞系暴露于集落刺激因子(CSF)和细胞因子后,对FcR表面表达进行了详细分析。在暴露于GCT或Mo细胞系条件培养基以及PHA处理的单核细胞培养基中的细胞中,FcRI和FcRII的表达在72小时时增加。FcRII的增加需要蛋白质合成,并且被抗粒细胞-巨噬细胞集落刺激因子的中和抗体所减弱。我们还表明,含有天然粒细胞集落刺激因子或粒细胞-巨噬细胞集落刺激因子以及重组粒细胞和重组粒细胞-巨噬细胞集落刺激因子的组分能够在这些细胞上诱导FcRII,而其他细胞因子如IL-1、IL-2、TNF-α、INF-γ和巨噬细胞集落刺激因子则不能。