Takeda Akiko, Matano Tetsuro
International Research Center for Infectious Diseases, The Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
Microbes Infect. 2007 Nov-Dec;9(14-15):1590-6. doi: 10.1016/j.micinf.2007.09.012. Epub 2007 Sep 23.
Fv-4 is a mouse gene that confers resistance against ecotropic murine leukemia virus (MLV) infection on mice. While receptor interference by the Fv-4 env gene product, Fv-4 Env, that can bind to the ecotropic MLV receptor has been shown to play an important role in the resistance, other mechanisms have also been suggested because it confers extremely efficient, complete resistance in vivo. Here, we have examined the effect of Fv-4 Env on infectious MLV production. Infectious MLV titers in supernatants obtained after transfection with a Friend MLV (FMLV) Env-expressing plasmid from MLV gag-pol producer cells harboring a retroviral vector were largely reduced by coexpression of Fv-4 Env. Syncytia formation mediated by R-peptide-deleted FMLV Env in NIH 3T3 cells was impaired by Fv-4 Env coexpression. Similarly, Fv-4 Env inhibited infectious amphotropic MLV production and syncytia formation mediated by R-peptide-deleted amphotropic MLV Env. Immunoprecipitation analysis revealed interaction of Fv-4 Env with amphotropic MLV Env as well as FMLV Env. These results indicate that Fv-4 Env inhibits infectious ecotropic and amphotropic MLV production by exerting dominant negative effect on MLV Env, suggesting contribution of this inhibitory effect to the resistance against ecotropic MLV infection in Fv-4-expressing mice.
Fv-4是一种小鼠基因,它能使小鼠对嗜亲性鼠白血病病毒(MLV)感染产生抗性。虽然已证明可与嗜亲性MLV受体结合的Fv-4 env基因产物Fv-4 Env对受体的干扰在这种抗性中起重要作用,但也有人提出了其他机制,因为它在体内能赋予极其高效、完全的抗性。在此,我们研究了Fv-4 Env对感染性MLV产生的影响。从携带逆转录病毒载体的MLV gag-pol产生细胞中转染表达Friend MLV(FMLV)Env的质粒后获得的上清液中的感染性MLV滴度,因共表达Fv-4 Env而大幅降低。在NIH 3T3细胞中,由R肽缺失的FMLV Env介导的合胞体形成因共表达Fv-4 Env而受到损害。同样,Fv-4 Env抑制了感染性双嗜性MLV的产生以及由R肽缺失的双嗜性MLV Env介导的合胞体形成。免疫沉淀分析揭示了Fv-4 Env与双嗜性MLV Env以及FMLV Env之间的相互作用。这些结果表明,Fv-4 Env通过对MLV Env发挥显性负效应来抑制感染性嗜亲性和双嗜性MLV的产生,提示这种抑制作用对表达Fv-4的小鼠抵抗嗜亲性MLV感染有贡献。