Gerlier D, Gisselbrecht S, Guillemain B, Doré J F
Br J Cancer. 1981 May;43(5):659-68. doi: 10.1038/bjc.1981.97.
The level of Gross cell-surface antigen (GCSAa) expression at the surface of murine retrovirus-infected fibroblasts was determined by quantitative absorption of the anti-GCSAa activity of a serum produced in syngeneic W/Fu rats immunized against (C58NT)D lymphoma, and tested in a cytotoxicity assay against E male G2 lymphoma cells. While GCSAa was specifically expressed on Gross-type virus (G-MuLV)-induced lymphoma cells, and while G-MuLV and G-related MuLV induced a high level of GCSAa expression on murine fibroblasts, the Friend-Moloney-Rauscher (FMR) group viruses (FMR MuLV) and xenotropic isolates were also able to induce a high or intermediate level of GCSAa. Since GCSAa has been shown to be borne by glycosylated precursors of the viral nucleocapside (gp95gag and gp85gag), the amount of GCSAa expressed on these cells was compared to the level of cytoplasmic p30. In G- and G-related MuLV-infected cell lines, a significant relationship was found between the amount of GCSAa and the level of p30, whereas in FMR-MuLV or xenotropic virus-infected cells the amount of GCSAa varied independently of the p30 level. These results could explain the discrepancy in the specificity of expression of GCSAa in vivo and in vitro.
通过定量吸收同基因W/Fu大鼠针对(C58NT)D淋巴瘤免疫产生的血清的抗GCSAa活性,测定了鼠逆转录病毒感染的成纤维细胞表面的总细胞表面抗原(GCSAa)表达水平,并在针对E雄性G2淋巴瘤细胞的细胞毒性试验中进行了测试。虽然GCSAa在格罗斯型病毒(G-MuLV)诱导的淋巴瘤细胞上特异性表达,并且G-MuLV和G相关的MuLV在鼠成纤维细胞上诱导了高水平的GCSAa表达,但弗瑞德-莫洛尼-劳舍尔(FMR)组病毒(FMR MuLV)和嗜异性分离株也能够诱导高水平或中等水平的GCSAa。由于已证明GCSAa由病毒核衣壳的糖基化前体(gp95gag和gp85gag)携带,因此将这些细胞上表达的GCSAa量与细胞质p30水平进行了比较。在G和G相关的MuLV感染的细胞系中,发现GCSAa量与p30水平之间存在显著关系,而在FMR-MuLV或嗜异性病毒感染的细胞中,GCSAa量的变化与p30水平无关。这些结果可以解释GCSAa在体内和体外表达特异性的差异。