Chang K C, Goldspink G, Lida J
Unit of Veterinary Molecular and Cell Biology, Royal Veterinary College, University of London, England.
Arch Virol. 1990;110(3-4):151-64. doi: 10.1007/BF01311285.
The inbred laboratory mouse strain A2G carries a functional, interferon type 1 inducible gene, Mx which upon expression confers specific resistance to an otherwise lethal dose of influenza virus. We investigated in vivo Mx gene expression by performing Northern hybridisation and in-situ hybridisation on A2G (Mx+) and (CBA/J x C57)F1 (Mx-) mice that were induced either with human, natural interferon; human, recombinant interferon or double stranded poly(I):(C). All 3 inducers were able to stimulate Mx expression in all organs examined in the A2G strain. However, contrary to previous reports, Mx expression was confined to a small number of cell types; the main contributor was most probably mononuclear cells. Specialised cells such as hepatocyte, nephron, ovarian follicle and seminiferous tubules did not show detectable Mx level. There was also constitutive Mx expression in the epithelia of uterus and duodenum which suggested direct gene activation independent of blood-bourne interferon.
近交系实验小鼠品系A2G携带一个功能性的Ⅰ型干扰素诱导基因Mx,该基因表达时可赋予小鼠对致死剂量流感病毒的特异性抗性。我们通过对A2G(Mx+)和(CBA/J×C57)F1(Mx-)小鼠进行Northern杂交和原位杂交,研究了体内Mx基因的表达情况,这些小鼠分别用人天然干扰素、人重组干扰素或双链聚肌苷酸:胞苷酸[poly(I):(C)]诱导。所有这3种诱导剂均能刺激A2G品系所有检测器官中的Mx表达。然而,与先前的报道相反,Mx表达局限于少数细胞类型;主要贡献者很可能是单核细胞。肝细胞、肾单位、卵泡和生精小管等特化细胞未显示出可检测到的Mx水平。子宫和十二指肠上皮中也存在组成型Mx表达,这表明存在不依赖于血液中干扰素的直接基因激活。