Lazarus A H, Baines M G
Cell Immunol. 1985 Dec;96(2):255-66. doi: 10.1016/0008-8749(85)90358-2.
Previous studies to determine the nature of the specificity of natural killer (NK) cells for leukemic cells indicated that functional transferrin (Tf) receptors may be one of the determinants recognized by NK cells. To further investigate these observations, the relationship between cellular Tf receptor expression and ability to compete with a control K562 cell preparation in a standard chromium release assay was studied. K562 cells were selected at different phases of growth by removing cells from tissue culture at 1, 3, and 5 days postfeeding. Under these conditions, K562 cells, respectively, displayed relatively high, medium, and low numbers of Tf receptors and corresponding competitive activity against a control K562 cell preparation. K562 cells were modified by either trypsin, heat, or sodium butyrate (differentiation inducer) pretreatment. An NK-resistant clone was also studied. There was a good correlation between Tf receptor expression and cold competitive activity of the above K562 cell preparations (r = 0.82, P less than 0.01). The different tumor target cell lines, K562, Molt-4, Raji, HL-60, and MeWo, which would be expected to express different ranges of specificity, did not show a significant correlation between Tf receptor expression and their cold competitive activities against Cr-51-labeled K562 cells. Rabbit reticulocytes which express high numbers of Tf receptors were tested for their ability to compete with K562 cells for NK cells. These cells were able to compete with K562 cells while mature rabbit red blood cells which do not express Tf receptors did not compete well. These findings support the contention that the Tf receptor may be involved in NK cell recognition of some tumor cells.
先前确定自然杀伤(NK)细胞对白血病细胞特异性本质的研究表明,功能性转铁蛋白(Tf)受体可能是NK细胞识别的决定因素之一。为了进一步研究这些观察结果,在标准铬释放试验中,研究了细胞Tf受体表达与与对照K562细胞制剂竞争能力之间的关系。通过在喂食后1、3和5天从组织培养中去除细胞,在不同生长阶段选择K562细胞。在这些条件下,K562细胞分别显示出相对较高、中等和较低数量的Tf受体以及对对照K562细胞制剂的相应竞争活性。通过胰蛋白酶、热或丁酸钠(分化诱导剂)预处理对K562细胞进行修饰。还研究了一个NK抗性克隆。上述K562细胞制剂的Tf受体表达与冷竞争活性之间存在良好的相关性(r = 0.82,P小于0.01)。预期表达不同特异性范围的不同肿瘤靶细胞系K562、Molt-4、Raji、HL-60和MeWo,其Tf受体表达与其对Cr-51标记的K562细胞的冷竞争活性之间未显示出显著相关性。对表达大量Tf受体的兔网织红细胞与K562细胞竞争NK细胞的能力进行了测试。这些细胞能够与K562细胞竞争,而不表达Tf受体的成熟兔红细胞则竞争不佳。这些发现支持了Tf受体可能参与NK细胞对某些肿瘤细胞识别的观点。