Pickering L A, Lin L S, Sarkar F H
Arch Virol. 1983;75(3):201-11. doi: 10.1007/BF01315274.
Several human lymphoblastoid cell lines produced significant levels of interferon (IFN) activity in the absence of any IFN induces. We have partially purified spontaneous IFN (SpIFN) from LuKII cells and compared it with the IFN activity produced by the same cells following Sendai virus induction. Virus-induced LuKII IFN reached maximum titers of 1000-6000 reference units/ml at 12 to 15 houts post-induction and produced a heterogeneous electrophoretic profile with major (18,500 dalton) and minor (23,500 dalton) species. Spontaneous LuKII IFN was produced very slowly over several days and reached maximum titers of 100-1000 reference units/ml. Crude SpIFN (25-100 ref. units/ml) was purified to 1-6 X 10(5) ref. units/ml with a 53-80 percent overall recovery, and it consistently migrated as a homogeneous 20,000 dalton band upon SDS gel electrophoresis. Although spontaneously produced and virus-induced lymphoblastoid IFNs differed in their ability to be neutralized by anti-mouse IFN antiserum (18), both types of IFN were only 1 percent cross-reactive on heterologous mouse L cells. We conclude that IFN definitely can be produced by many human lymphoblastoid cell lines in the absence of inducers, and that LuKII SpIFN has different characteristics than the IFNs produced by the same cell line following viral induction. Since it is now known that there are many IFN-alpha genes (3, 10), it seems likely that these cell lines may provide a system for studying the selective expression of one or more of these genes.
几种人淋巴母细胞系在没有任何干扰素诱导剂的情况下产生了显著水平的干扰素(IFN)活性。我们已从LuKII细胞中部分纯化了自发干扰素(SpIFN),并将其与仙台病毒诱导后同一细胞产生的IFN活性进行了比较。病毒诱导的LuKII IFN在诱导后12至15小时达到最高滴度1000 - 6000参考单位/毫升,并产生了具有主要(18,500道尔顿)和次要(23,500道尔顿)成分的异质电泳图谱。自发的LuKII IFN在几天内产生得非常缓慢,最高滴度达到100 - 1000参考单位/毫升。粗制的SpIFN(25 - 100参考单位/毫升)被纯化至1 - 6×10⁵参考单位/毫升,总体回收率为53 - 80%,并且在SDS凝胶电泳中始终迁移为单一的20,000道尔顿条带。尽管自发产生的和病毒诱导的淋巴母细胞IFN在被抗小鼠IFN抗血清中和的能力上有所不同(18),但两种类型的IFN在异源小鼠L细胞上的交叉反应性仅为1%。我们得出结论,IFN肯定可以由许多人淋巴母细胞系在没有诱导剂的情况下产生,并且LuKII SpIFN与同一细胞系在病毒诱导后产生的IFN具有不同的特性。由于现在已知有许多IFN-α基因(3, 10),这些细胞系似乎有可能提供一个系统来研究这些基因中一个或多个的选择性表达。