Qi W, Tamura Y, Takashima S, Sato N, Kikuchi K
Department of Pathology, Sapporo Medical University School of Medicine.
Jpn J Cancer Res. 1994 Aug;85(8):862-8. doi: 10.1111/j.1349-7006.1994.tb02959.x.
We previously reported on the 86 kDa natural killer target molecule associated with transformation of the oncogene-transfected rat fibroblasts. This molecule may participate in the lethal hit phase of cytotoxicity by natural killer (NK) cells. Originally, this molecule was defined by mAb109, but mAb109 could react only with rat tumor lines. In this report, to determine whether the 86 kDa molecule could be utilized as a natural killer target molecule in mammalian cells, we developed a polyclonal anti-86 kDa antibody (pAb109). Our data indicated that pAb109 preferentially reacted with NK-susceptible lines such as mouse YAC-1, rat W31 and human K562 cells, but reacted only weakly with NK-resistant mouse EL-4, rat fetal fibroblast WFB and human fetal fibroblast HEPM. In a cytotoxicity experiment, pAb109 F(ab')2 fragments could inhibit the cytolysis by NK cells of W31 and K562 cells. However, these fragments did not inhibit the cytotoxicity of non-NK cells such as CD3+, CD4-, CD8- T cell receptor alpha beta- T cells (presumably gamma delta T cells) to W31 cells. Taken together, these data suggest that the cell transformation-associated 86 kDa molecule may be critical in NK cytotoxicity, and a candidate for the NK target structure in mammalian tumor cells.
我们先前报道过与癌基因转染大鼠成纤维细胞转化相关的86 kDa自然杀伤细胞靶分子。该分子可能参与自然杀伤(NK)细胞细胞毒性的致死性打击阶段。最初,该分子由单克隆抗体109(mAb109)鉴定,但mAb109仅能与大鼠肿瘤细胞系发生反应。在本报告中,为了确定86 kDa分子是否可作为哺乳动物细胞中的自然杀伤细胞靶分子,我们制备了一种抗86 kDa多克隆抗体(pAb109)。我们的数据表明,pAb109优先与NK敏感细胞系发生反应,如小鼠YAC-1、大鼠W31和人K562细胞,但与NK抗性的小鼠EL-4、大鼠胎儿成纤维细胞WFB和人胎儿成纤维细胞HEPM的反应较弱。在细胞毒性实验中,pAb109 F(ab')2片段可抑制NK细胞对W31和K562细胞的细胞溶解作用。然而,这些片段并不抑制非NK细胞如CD3 +、CD4 -、CD8 - T细胞受体αβ - T细胞(可能是γδ T细胞)对W31细胞的细胞毒性。综上所述,这些数据表明与细胞转化相关的86 kDa分子可能在NK细胞毒性中起关键作用,并且是哺乳动物肿瘤细胞中NK靶结构的候选分子。