Van Damme J, Opdenakker G, Billiau A, De Somer P, De Wit L, Poupart P, Content J
J Gen Virol. 1985 Apr;66 ( Pt 4):693-700. doi: 10.1099/0022-1317-66-4-693.
We have studied the appearance of human interferon-beta (HuIFN-beta) as well as its mRNA in cells treated with a protein, 22K factor, isolated from the culture supernatant of mitogen-stimulated human peripheral blood leukocytes. By itself 22K was found to be unable to induce production of significant amounts of HuIFN-beta protein. However, when aided by treatment with cycloheximide or cycloheximide and actinomycin D (superinduction), 22K caused increases in production ranging from 3- to 20-fold, depending on the cells (diploid or MG-63 osteosarcoma) and the induction schedule. Cells treated with 22K alone produced small amounts of HuIFN-beta mRNA, which was only detectable with a highly sensitive method. In combination with cycloheximide, 22K induced levels of mRNA detectable with less sensitive methods as well. These experiments provide further support for the concept that the antiviral activity of 22K is mediated by its ability to stimulate transcription of the HuIFN-beta gene in cells.
我们研究了人β干扰素(HuIFN-β)及其mRNA在经一种从丝裂原刺激的人外周血白细胞培养上清液中分离出的蛋白质(22K因子)处理的细胞中的出现情况。单独的22K被发现无法诱导产生大量的HuIFN-β蛋白。然而,当用环己酰亚胺或环己酰亚胺与放线菌素D处理(超诱导)辅助时,22K会导致产量增加3至20倍,这取决于细胞类型(二倍体细胞或MG-63骨肉瘤细胞)和诱导方案。单独用22K处理的细胞产生少量的HuIFN-β mRNA,只有用高度灵敏的方法才能检测到。与环己酰亚胺联合使用时,22K也能诱导出用不太灵敏的方法就能检测到的mRNA水平。这些实验为22K的抗病毒活性是由其刺激细胞中HuIFN-β基因转录的能力介导这一概念提供了进一步的支持。