Bourgeade M F, Laurent-Winter C, Besançon F, Thang M N, Mémet S
U245 INSERM, Hôpital St. Antoine, Paris, France.
J Interferon Res. 1993 Jun;13(3):175-86. doi: 10.1089/jir.1993.13.175.
Using two-dimensional electrophoresis on total and nuclear extracts of human fibroblasts, we compared polypeptide patterns of cells treated with interferon-beta (IFN-beta), IFN-gamma, or with dsRNA in the presence of anti-IFN antibodies. The analysis of whole-cell extracts revealed that, after a 6-h treatment, the three agents induce the synthesis of a common set of proteins in addition to others that are specifically induced either by IFNs or by dsRNA. After a 15-h treatment, this common set of proteins was only induced by IFNs. Furthermore, at this time, IFNs also regulated proteins whose synthesis was specifically induced or repressed by poly(I).poly(C) in the 6-h treated cells. These results indicate that poly(I).poly(C) regulates protein expression more rapidly and more transiently than IFNs. The analysis of nuclear extracts showed similar differential kinetics of protein expression. However, a greater number of polypeptides was found to have their synthesis specifically induced by dsRNA. Moreover, poly(I).poly(C) was found to be mitogenic in these cells and did not induce a significant resistance to vesicular stomatitis virus (VSV). This study provides evidence for an overlap in the expression of proteins by dsRNA and IFNs, although these compounds do not share the same biological activities.
我们运用二维电泳技术,对人成纤维细胞的总提取物和核提取物进行分析,比较了用β干扰素(IFN-β)、γ干扰素(IFN-γ)处理的细胞,以及在存在抗干扰素抗体的情况下用双链RNA(dsRNA)处理的细胞的多肽图谱。对全细胞提取物的分析表明,经过6小时处理后,这三种试剂除了诱导产生一组由干扰素或双链RNA特异性诱导的蛋白质外,还诱导合成了一组共同的蛋白质。经过15小时处理后,这组共同的蛋白质仅由干扰素诱导产生。此外,此时干扰素还调节了在6小时处理的细胞中由聚肌苷酸-聚胞苷酸(poly(I).poly(C))特异性诱导或抑制合成的蛋白质。这些结果表明,与干扰素相比,聚肌苷酸-聚胞苷酸对蛋白质表达的调节更快且更短暂。对核提取物的分析显示出类似的蛋白质表达差异动力学。然而,发现更多的多肽其合成是由双链RNA特异性诱导的。此外,发现聚肌苷酸-聚胞苷酸在这些细胞中具有促有丝分裂作用,并且不会诱导对水疱性口炎病毒(VSV)产生显著抗性。这项研究为双链RNA和干扰素在蛋白质表达上存在重叠提供了证据,尽管这些化合物并不具有相同的生物学活性。