Aboud M, Huleihel M
Arch Virol. 1981;70(2):103-14. doi: 10.1007/BF01315004.
Moloney murine sarcoma virus (MSV) clone 124 was found to induce rapid syncytium formation upon infection of 3T3/NIH at a high multiplicity of infection. This effect became apparent, by light microscopy, within 1 to 2 hours, whereas by scanning electron microscopy, clusters of 4 to 25 cells were seen in their initial steps of syncytium formation within 20 to 30 minutes after virus addition. It appeared that the cell fusion was initiated by connection between the cells through virus bound to their surface. After a few more hours several neighbouring syncytia fused into giant cells containing over a hundred nuclei. Though MSV (124) stocks contained also some MLV it appeared that the syncytium inducing activity was related to the MSV particles. MLV particles were not only incapable to induce syncytium formation, they even interfered with this activity of MSV. The MSV-induced cell fusion required the adsorption of intact virions, but was independent on protein synthesis. Mouse interferon remarkably reduced the rate of syncytium development.
莫洛尼鼠肉瘤病毒(MSV)克隆124在高感染复数感染3T3/NIH细胞时,被发现可诱导快速的合胞体形成。通过光学显微镜观察,这种效应在1至2小时内变得明显,而通过扫描电子显微镜观察,在添加病毒后20至30分钟内,在合胞体形成的初始步骤中可见4至25个细胞的簇。似乎细胞融合是由通过结合在细胞表面的病毒连接细胞之间而启动的。再过几个小时,几个相邻的合胞体融合成含有一百多个细胞核的巨细胞。尽管MSV(124)毒株中也含有一些MLV,但合胞体诱导活性似乎与MSV颗粒有关。MLV颗粒不仅不能诱导合胞体形成,甚至还会干扰MSV的这种活性。MSV诱导的细胞融合需要完整病毒粒子的吸附,但与蛋白质合成无关。小鼠干扰素显著降低了合胞体发育的速率。