Rubio N, Rojo P, Torres C
Department of Neuroimmunology, Instituto Cajal, Madrid, Spain.
J Neurovirol. 1996 Jun;2(3):167-74. doi: 10.3109/13550289609146879.
Constitutive expression of the cellular proto-oncogenes c-fos and c-jun, and in a lesser extent ras, was demonstrated in the glioma cell line C-6 by flow cytometry analysis using specific mono and polyclonal antibodies. Basal expression of the products of the early response genes c-fos and c-jun were increased 66 and 50% when Theiler's murine encephalomyelitis virus (TMEV) infected these cells. No increase in ras transcription could be demonstrated after infection. This activation follows a kinetic reaching maximum values after 60 min and was proportional to the multiplicity of infection used. The described effect was completely abrogated by rabbit antibodies to TMEV but was not altered by normal rabbit serum. Furthermore, an intact infectious virion is needed to detect this effect. Fetal calf serum and lipopolysaccharide stimulation slightly increases c-fos and c-jun expression following a slower kinetics. Cytokine treatment (IL-1 alpha, IL-6, IFN-gamma and TNF alpha), did not induce oncogene over-expression. Therefore, this stimulation seems to be linked to the TMEV infectious process.
通过使用特异性单克隆和多克隆抗体的流式细胞术分析,在胶质瘤细胞系C-6中证实了细胞原癌基因c-fos和c-jun以及程度较轻的ras的组成型表达。当泰勒氏鼠脑脊髓炎病毒(TMEV)感染这些细胞时,早期反应基因c-fos和c-jun产物的基础表达分别增加了66%和50%。感染后未发现ras转录增加。这种激活呈现出一种动力学特征,在60分钟后达到最大值,并且与所用的感染复数成正比。上述效应被抗TMEV的兔抗体完全消除,但未被正常兔血清改变。此外,需要完整的感染性病毒粒子来检测这种效应。胎牛血清和脂多糖刺激后,c-fos和c-jun表达略有增加,但动力学较慢。细胞因子处理(IL-1α、IL-6、IFN-γ和TNFα)未诱导癌基因过度表达。因此,这种刺激似乎与TMEV感染过程有关。