Nanbo Asuka, Inoue Kaori, Adachi-Takasawa Kumi, Takada Kenzo
Department of Tumor Virology, Institute for Genetic Medicine, Hokkaido University, N15 W7, Kita-ku, Sapporo 060-0815, Japan.
EMBO J. 2002 Mar 1;21(5):954-65. doi: 10.1093/emboj/21.5.954.
We investigated whether Epstein--Barr virus (EBV) infection could counteract the antitumor effect of interferon (IFN)-alpha. EBV-negative subclones isolated from EBV-positive Burkitt's lymphoma (BL) cell lines Akata, Daudi and Mutu were found to fall into apoptosis after IFN-alpha treatment. On the other hand, EBV-positive counterparts exhibited striking resistance against IFN-alpha-induced apoptosis. Transfection of an individual EBV latent gene into EBV-negative BL cells revealed that EBV-encoded poly(A)(-) RNAs (EBERs) were responsible for IFN resistance. EBERs bound double-stranded (ds) RNA-activated protein kinase (PKR), a key mediator of the antiviral effect of IFN-alpha, and inhibited its phosphorylation. Transfection of dominant-negative PKR, which was catalytically inactive and could block phosphorylation of endogenous PKR, made EBV-negative BL cells resistant to IFN-alpha-induced apoptosis. Furthermore, EBERs did not bind mutant PKR, which was catalytically active but lacked dsRNA-binding activity, nor did they inhibit its phosphorylation. These results indicate that EBERs confer resistance to IFN-alpha-induced apoptosis via binding to PKR and inhibition of its phosphorylation. This is the first report that the virus counteracts IFN-induced apoptosis in virus-associated tumors.
我们研究了爱泼斯坦-巴尔病毒(EBV)感染是否会抵消干扰素(IFN)-α的抗肿瘤作用。从EBV阳性的伯基特淋巴瘤(BL)细胞系Akata、Daudi和Mutu中分离出的EBV阴性亚克隆在接受IFN-α治疗后发生凋亡。另一方面,EBV阳性的对应亚克隆对IFN-α诱导的凋亡表现出显著抗性。将单个EBV潜伏基因转染到EBV阴性BL细胞中发现,EBV编码的多聚腺苷酸(-)RNA(EBERs)是导致IFN抗性的原因。EBERs与双链(ds)RNA激活蛋白激酶(PKR)结合,PKR是IFN-α抗病毒作用的关键介质,并抑制其磷酸化。转染显性负性PKR(其催化无活性且可阻断内源性PKR的磷酸化)使EBV阴性BL细胞对IFN-α诱导的凋亡产生抗性。此外,EBERs不与催化活性但缺乏dsRNA结合活性的突变型PKR结合,也不抑制其磷酸化。这些结果表明,EBERs通过与PKR结合并抑制其磷酸化赋予对IFN-α诱导凋亡的抗性。这是关于病毒在病毒相关肿瘤中抵消IFN诱导凋亡的首次报道。