Li J P, Hu H O, Niu Q T, Fang C
Department of Microbiology, New York University Medical Center, New York 10016.
J Virol. 1995 Mar;69(3):1714-19. doi: 10.1128/JVI.69.3.1714-1719.1995.
The leukemogenic membrane glycoprotein gp55, encoded by Friend spleen focus-forming virus (SFFV), induces erythroid cell proliferation through its interaction with the erythropoietin receptor (EPO-R). There are two forms of gp55 in SFFV-infected cells: an intracellular form (more than 95% of the total protein), which is localized within the endoplasmic reticulum (ER) membranes, and a cell surface form (about 3 to 5%). Because both forms of the viral proteins bind to EPO-R, it is not clear whether the viral protein induces mitogenesis intracellularly or at the cell surface. To address this question, we constructed an EPO-R mutant that contained a 6-amino-acid (DEKKMP) C-terminus ER retention signal. Biochemical and functional analyses with this mutant indicated that it was completely retained in the ER and not expressed at the cell surface. Further analysis showed that the mutant, like the wild-type EPO-R, interacted with SFFV gp55. However, this apparent intracellular interaction between the two proteins failed to induce growth factor-independent proliferation of Ba/F3 cells. Furthermore, spontaneous variants of the ER-retained EPO-R selected on the basis of their ability to induce cell proliferation when coexpressed with gp55 were exclusively expressed at the cell surface. Thus, our results support the hypothesis that the mitogenic activation of the EPO-R by gp55 requires the interaction of the two proteins at the cell surface.
由弗瑞德脾集落形成病毒(SFFV)编码的致白血病膜糖蛋白gp55,通过与促红细胞生成素受体(EPO-R)相互作用诱导红细胞增殖。在感染SFFV的细胞中有两种形式的gp55:一种是细胞内形式(占总蛋白的95%以上),定位于内质网(ER)膜内;另一种是细胞表面形式(约3%至5%)。由于这两种形式的病毒蛋白都能与EPO-R结合,因此尚不清楚病毒蛋白是在细胞内还是在细胞表面诱导有丝分裂。为了解决这个问题,我们构建了一个含有6个氨基酸(DEKKMP)C末端内质网滞留信号的EPO-R突变体。对该突变体的生化和功能分析表明,它完全滞留在内质网中,不在细胞表面表达。进一步分析表明,该突变体与野生型EPO-R一样,能与SFFV gp55相互作用。然而,这两种蛋白之间明显的细胞内相互作用未能诱导Ba/F3细胞的生长因子非依赖性增殖。此外,基于与gp55共表达时诱导细胞增殖的能力而筛选出的内质网滞留EPO-R自发变体仅在细胞表面表达。因此,我们的结果支持这样一种假说,即gp55对EPO-R的有丝分裂激活需要这两种蛋白在细胞表面相互作用。