Dreiding P, Staeheli P, Haller O
Virology. 1985 Jan 15;140(1):192-6. doi: 10.1016/0042-6822(85)90460-x.
In mouse cells carrying the dominant influenza resistance allele Mx+ (but not in Mx- cells) interferon-alpha/beta (IFN) induces an efficient antiviral state against influenza viruses and, concomitantly, the synthesis of a 75,000-Da protein (protein Mx). Here, indirect immunofluorescence using monoclonal antibodies was used to demonstrate that protein Mx accumulates in the nucleus of IFN-treated Mx+ cells, suggesting a nuclear site of action. Protein Mx is present in the nucleus of untreated influenza virus-resistant macrophages freshly explanted from the peritoneal cavity of Mx+ mice but is lost with time in culture when peritoneal macrophages become permissive for influenza virus.
在携带显性抗流感等位基因Mx+的小鼠细胞中(但在Mx-细胞中则不然),α/β干扰素(IFN)可诱导产生高效的抗流感病毒状态,并同时合成一种75000道尔顿的蛋白质(Mx蛋白)。在此,利用单克隆抗体进行间接免疫荧光实验,以证明Mx蛋白在经IFN处理的Mx+细胞的细胞核中积累,这表明其作用位点在细胞核。Mx蛋白存在于刚从Mx+小鼠腹腔中分离出的未经处理的抗流感病毒巨噬细胞的细胞核中,但在培养过程中,随着时间的推移,当腹腔巨噬细胞对流感病毒变得易感时,该蛋白会逐渐消失。