Megyeri K, Berencsi K, Halazonetis T D, Prendergast G C, Gri G, Plotkin S A, Rovera G, Gönczöl E
The Wistar Institute, 3601 Spruce Street, Philadelphia, Pennsylvania, 19104, USA.
Virology. 1999 Jun 20;259(1):74-84. doi: 10.1006/viro.1999.9757.
In light of the important role of apoptotic cell death in the pathogenesis of several viral infections, we asked whether the cytopathogenicity evoked by rubella virus (RV) might also involve apoptotic mechanisms. The To-336 strain of RV induced apoptosis in Vero and RK-13 cells, but not in fibroblast cell lines. UV-inactivated RV virions did not elicit the apoptotic response, indicating that productive infection is required for the induction of cell death. Both p53 and p21 protein levels were highly elevated in RV-infected Vero cells. The level of p21 mRNA was increased, while expression of the p53 gene was unaffected by RV infection. A dominant-negative p53 mutant (p53(W248)) conferred partial protection from RV-induced apoptosis. These data implicate a p53-dependent apoptotic pathway in the cytopathogenicity of RV, thereby suggesting a mechanism by which RV exerts its teratogenic effects.
鉴于凋亡性细胞死亡在几种病毒感染发病机制中的重要作用,我们探讨风疹病毒(RV)引发的细胞病变效应是否也涉及凋亡机制。RV的To-336株可诱导Vero和RK-13细胞发生凋亡,但不能诱导成纤维细胞系发生凋亡。紫外线灭活的RV病毒粒子未引发凋亡反应,表明细胞死亡的诱导需要病毒的有效感染。在RV感染的Vero细胞中,p53和p21蛋白水平均显著升高。p21 mRNA水平升高,而p53基因的表达不受RV感染的影响。显性负性p53突变体(p53(W248))对RV诱导的凋亡具有部分保护作用。这些数据表明,p53依赖性凋亡途径参与了RV的细胞病变效应,从而提示了RV发挥致畸作用的一种机制。