Staeheli P, Horisberger M A, Haller O
Virology. 1984 Jan 30;132(2):456-61. doi: 10.1016/0042-6822(84)90050-3.
In cells derived from congenic BALB.A2G-Mx mice carrying the resistance gene Mx, but not in cells from BALB/c mice lacking Mx, mouse interferons alpha and beta induced the synthesis of a unique cellular protein that was associated with an efficient antiviral state with selectivity for influenza viruses. In contrast, native or recombinant mouse interferon gamma failed to efficiently protect Mx-bearing cells against influenza viruses and did not noticeably induce the synthesis of the Mx-associated protein, although interferon gamma was as effective as interferons alpha and beta in protecting BALB.A2G-Mx and BALB/c cells against the rhabdovirus VSV. These results demonstrate that different types of interferons differentially regulate the expression of the Mx gene and thereby induce distinct antiviral states.
在携带抗性基因Mx的同源BALB.A2G-Mx小鼠来源的细胞中,而非在缺乏Mx的BALB/c小鼠的细胞中,小鼠α干扰素和β干扰素可诱导一种独特的细胞蛋白的合成,该蛋白与针对流感病毒具有选择性的高效抗病毒状态相关。相比之下,天然或重组小鼠γ干扰素未能有效保护携带Mx的细胞免受流感病毒感染,也未显著诱导与Mx相关蛋白的合成,尽管γ干扰素在保护BALB.A2G-Mx和BALB/c细胞免受弹状病毒VSV感染方面与α干扰素和β干扰素一样有效。这些结果表明,不同类型的干扰素对Mx基因的表达有不同的调节作用,从而诱导出不同的抗病毒状态。