Zarling D A, Keshet I, Watson A, Bach F H
Scand J Immunol. 1978;8(6):497-508. doi: 10.1111/j.1365-3083.1978.tb00549.x.
Physical association was measured between MLV gp70, the envelope glycoprotein of Rauscher murine leukaemia virus (R-MLV), and serologically defined H-2 antigens on the surface of R-MLV transformed C57BL/6 (H-2DbKb) mouse leukaemia cells (RBL-5A). Capping and patching with antisera against H-2Db caused specific co-capping and co-patching of R-MLV gp70 antigens as seen by fluorescence microscopy. Despite the physical proximity of R-MLV gp70 and H-2Db antigens, high titre alphaR-MLV gp70 sera had no effect in blocking syngeneic T-lymphocyte mediated cytolysis of RBL-2A cells whereas alphaH-2Db sera were effective.
对劳舍尔小鼠白血病病毒(R-MLV)的包膜糖蛋白MLV gp70与R-MLV转化的C57BL/6(H-2DbKb)小鼠白血病细胞(RBL-5A)表面血清学定义的H-2抗原之间的物理关联进行了检测。通过荧光显微镜观察,用抗H-2Db抗血清进行封帽和贴片导致R-MLV gp70抗原特异性共封帽和共贴片。尽管R-MLV gp70和H-2Db抗原在物理上接近,但高滴度的αR-MLV gp70血清对阻断同基因T淋巴细胞介导的RBL-2A细胞的细胞溶解没有作用,而αH-2Db血清则有效。