Ando I, Hoon D S, Suzuki Y, Saxton R E, Golub S H, Irie R F
Int J Cancer. 1987 Jul 15;40(1):12-7. doi: 10.1002/ijc.2910400104.
Although human NK cells lyse a wide spectrum of target cells, the precise target structure recognized by NK cells has not yet been elucidated. In order to define a possible relationship between gangliosides on human target cells and susceptibility to NK lysis, 14 human leukemia and lymphoma cell lines were studied. A significant correlation was observed between the quantity of ganglioside GM2 on the target cells and sensitivity to NK lysis. In a single-cell binding assay purified GM2 specifically inhibited human NK cell binding to K562 target cells while other gangliosides did not inhibit binding. The competitive inhibition of NK cells by GM2 was restricted to the source of tissue from which GM2 was isolated. These results indicate that GM2 is a strong candidate as a target recognition structure for human NK cells.
尽管人类自然杀伤(NK)细胞可裂解多种靶细胞,但NK细胞识别的精确靶结构尚未阐明。为了确定人类靶细胞上神经节苷脂与NK细胞裂解敏感性之间的可能关系,对14种人类白血病和淋巴瘤细胞系进行了研究。观察到靶细胞上神经节苷脂GM2的量与对NK细胞裂解的敏感性之间存在显著相关性。在单细胞结合试验中,纯化的GM2特异性抑制人类NK细胞与K562靶细胞的结合,而其他神经节苷脂则不抑制结合。GM2对NK细胞的竞争性抑制仅限于分离出GM2的组织来源。这些结果表明,GM2是人类NK细胞靶识别结构的有力候选者。