Ceredig R, Robins T, Campbell H D, Young I G, Hapel A J
Department of Medicine and Clinical Science, John Curtin School of Medical Research, Australian National University, Canberra.
J Natl Cancer Inst. 1988 Apr 6;80(3):165-70. doi: 10.1093/jnci/80.3.165.
An autocrine leukemia (FDC-P1-IL3) has been developed using a retroviral vector containing the interleukin-3 (IL-3) gene to transfect the IL-3-dependent cell line FDC-P1. When leukemia cells were reisolated from experimental animals, it was found that levels of interleukin-2 (IL-2) receptor (IL-2R) expression were greater on cells isolated from the lymph node than on cells isolated from the spleen. Cloned sublines of FDC-P1-IL3 were selected by flow microfluorometry for high or low levels of IL-2R expression. Those clones that expressed high levels of IL-2R grew preferentially in the lymph node. Although IL-2 is not mitogenic for FDC-P1 cells and does not increase the rate of growth of FDC-P1-IL3 cells in vitro, the cloning efficiency of FDC-P1-IL3 is increased fourfold in the presence of IL-2. These observations suggest that the IL-2R on FDC-P1-IL3 cells plays an important role in modulating the growth of this leukemia in sites that contain high levels of IL-2.
利用含有白细胞介素-3(IL-3)基因的逆转录病毒载体转染依赖IL-3的细胞系FDC-P1,构建了一种自分泌性白血病(FDC-P1-IL3)。当从实验动物中重新分离白血病细胞时,发现从淋巴结分离的细胞上白细胞介素-2(IL-2)受体(IL-2R)的表达水平高于从脾脏分离的细胞。通过流式细胞荧光分选术选择FDC-P1-IL3的克隆亚系,以获得高表达或低表达IL-2R的细胞。那些高表达IL-2R的克隆在淋巴结中优先生长。虽然IL-2对FDC-P1细胞无促有丝分裂作用,且在体外不会提高FDC-P1-IL3细胞的生长速率,但在IL-2存在的情况下,FDC-P1-IL3的克隆效率提高了四倍。这些观察结果表明,FDC-P1-IL3细胞上的IL-2R在含有高水平IL-2的部位调节这种白血病的生长中起重要作用。