Sherman L, Eylan E, Teitz Y
Arch Virol. 1980;66(2):143-55. doi: 10.1007/BF01314982.
Interferon treatment of mouse cells chronically infected with Moloney leukemia virus (3T3/MLV) resulted in 97 per cent inhibition of infective virus release. The intracellular localization and distribution of virus reverse-transcriptase and group specific (gs) antigen were determined in interferon treated and control cells. Cytoplasm of infected cells was fractionated by isopycnic centrifugation on discontinuous sucrose gradients. Fractions were analysed for their chemical composition and characterized by the activity of membranal marker enzymes. The association and levels of viral antigens were determined in each fraction. Fractions enriched with 5' nucleotidase, specific enzyme marker for plasma membrane, were also enriched with viral proteins. In interferon treated cells, intracellular accumulation of viral proteins was specifically localized in the plasma membrane. Threefold increase in reverse-transcriptase level was the maximal accumulation found in purified plasma membranes. Intracellular enzyme levels in interferon treated cells were in accordance with the amount of cell associated infective virus particles. The small accumulation of viral proteins and infective virus particles was not sufficient to account for the great reduction in virus yield observed in the supernatants of the interferon treated cells. A possible role for interferon in modification of plasma membrane associated with virus assembly is postulated.
用干扰素处理长期感染莫洛尼白血病病毒的小鼠细胞(3T3/MLV),可使感染性病毒释放受到97%的抑制。在经干扰素处理的细胞和对照细胞中,对病毒逆转录酶和群特异性(gs)抗原的细胞内定位及分布进行了测定。通过在不连续蔗糖梯度上进行等密度离心,对感染细胞的细胞质进行分级分离。分析各分级分离物的化学成分,并通过膜标记酶的活性对其进行表征。测定每个分级分离物中病毒抗原的结合情况和水平。富含质膜特异性酶标记物5'核苷酸酶的分级分离物,也富含病毒蛋白。在经干扰素处理的细胞中,病毒蛋白的细胞内积累特异性地定位于质膜。逆转录酶水平增加三倍是在纯化质膜中发现的最大积累量。经干扰素处理的细胞中的细胞内酶水平与细胞相关感染性病毒颗粒的数量一致。病毒蛋白和感染性病毒颗粒的少量积累不足以解释在经干扰素处理的细胞上清液中观察到的病毒产量的大幅降低。推测干扰素在与病毒组装相关的质膜修饰中可能发挥作用。