Voshol H, Dullens H F, Den Otter W, Vliegenthart J F
Utrecht University, Bijvoet Center, Department of Bio-Organic Chemistry, The Netherlands.
Glycobiology. 1993 Feb;3(1):69-76. doi: 10.1093/glycob/3.1.69.
Natural killer (NK) cells can spontaneously kill various malignant cells, but the susceptibility towards NK cells differs greatly among different types of tumour cells. The molecules, which are recognized by NK cells, have not yet been identified, but there is ample evidence that target cell surface glycoconjugates are involved in the interaction with NK cells. In this report, we show that the recognition of K562 target cells by human NK cells depends on the presence of protein-bound determinants, implying that glycolipids are not the primary target structures on K562 cells. The NK susceptibility of K562 cells was not altered by enzymic removal of various cell surface carbohydrates or oligosaccharides, mostly related to N-linked carbohydrate chains. Treatment of K562 cells with 1-deoxynojirimycin and 1-deoxymannojirimycin, inhibitors of N-glycan processing, resulted in drastic alterations in the carbohydrate phenotype of the cell surface, as could be shown by flow cytometric analysis of the lectin-binding properties of the cells. Despite these clear changes in N-glycosylation, the NK susceptibility of K562 cells remained unaffected. Summarizing, the results described in this report show that potential target structures for NK cells are protein bound, but the involvement of a specific (N-linked) carbohydrate determinant in the interaction between NK cells and target cells could not be established.
自然杀伤(NK)细胞能够自发地杀伤各种恶性细胞,但不同类型的肿瘤细胞对NK细胞的敏感性差异很大。NK细胞识别的分子尚未确定,但有充分证据表明靶细胞表面糖缀合物参与了与NK细胞的相互作用。在本报告中,我们表明人类NK细胞对K562靶细胞的识别取决于蛋白质结合决定簇的存在,这意味着糖脂不是K562细胞上的主要靶结构。通过酶法去除各种细胞表面碳水化合物或寡糖(大多与N-连接碳水化合物链相关),K562细胞的NK敏感性并未改变。用N-聚糖加工抑制剂1-脱氧野尻霉素和1-脱氧甘露野尻霉素处理K562细胞,导致细胞表面碳水化合物表型发生剧烈变化,这可通过对细胞凝集素结合特性的流式细胞术分析得以显示。尽管N-糖基化发生了这些明显变化,K562细胞的NK敏感性仍未受影响。总之,本报告所述结果表明,NK细胞的潜在靶结构是与蛋白质结合的,但无法确定特定的(N-连接)碳水化合物决定簇是否参与NK细胞与靶细胞之间的相互作用。