Zaunders J, Werkmeister J, McCarthy W H, Hersey P
Br J Cancer. 1981 Jan;43(1):5-12. doi: 10.1038/bjc.1981.2.
Inhibitors of natural killer (NK) cell activity in cell-culture supernatants, believed to be antigens recognized by NK cells, were defined by their ability to inhibit NK cells in 51Cr-release cytotoxic assays. Supernatants from cultures of melanoma cells and Chang cells were used as the source of the antigen. Partial characterization by a number of sequential separation procedures suggested that the antigens were glycoproteins in the size range 120-140,000 daltons which had affinity for both concanavalin A and wheat germ lectin. Inhibitory activity was destroyed by trypsin digestion, but was resistant to neuraminidase and a number of physical procedures. Addition of supernatants to NK assays against a number of different target cells indicated that inhibition was restricted to certain target cells. This indicated that the inhibition of NK cells was not non-specific, and that the antigens were not expressed on all target cells. These studies provide a basis for further analysis of antigens recognized by NK cells, and allow investigation of their role in vivo in tumour-bearing hosts.
细胞培养上清液中自然杀伤(NK)细胞活性的抑制剂,被认为是NK细胞识别的抗原,通过其在51Cr释放细胞毒性试验中抑制NK细胞的能力来定义。黑色素瘤细胞和张氏细胞培养物的上清液用作抗原来源。通过一系列连续分离程序进行的部分特性分析表明,这些抗原是大小在120 - 140,000道尔顿范围内的糖蛋白,对伴刀豆球蛋白A和麦胚凝集素都有亲和力。抑制活性被胰蛋白酶消化破坏,但对神经氨酸酶和一些物理处理具有抗性。将上清液添加到针对多种不同靶细胞的NK试验中表明,抑制作用仅限于某些靶细胞。这表明对NK细胞的抑制不是非特异性的,并且抗原并非在所有靶细胞上表达。这些研究为进一步分析NK细胞识别的抗原提供了基础,并有助于研究它们在荷瘤宿主体内的作用。