Le Clorennec Christophe, Ouk Tan-Sothéa, Youlyouz-Marfak Ibtissam, Panteix Stéphanie, Martin Catherine-Claude, Rastelli Julia, Adriaenssens Eric, Zimber-Strobl Ursula, Coll Jean, Feuillard Jean, Jayat-Vignoles Chantal
UMR CNRS 6101, Faculté de Medecine, 2 rue du Docteur Marchand, 87025 Limoges Cedex, France.
J Virol. 2008 Jul;82(13):6721-33. doi: 10.1128/JVI.02250-07. Epub 2008 Apr 30.
The Epstein-Barr virus (EBV) oncoprotein latent membrane protein 1 (LMP1) is thought to act as the major transforming protein in various cell types, by rerouting the tumor necrosis factor receptor family signaling pathway. Despite this implication in EBV-associated transformation of cells, LMP1 toxicity is a well-known but poorly studied feature, perhaps because it contradicts its role in transformation. We show that LMP1 physiological levels are very heterogeneous and that the highest levels of LMP1 correlate with Fas overexpression and spontaneous apoptosis in lymphoblastoid cell lines (LCLs). To understand the cytotoxic effect of LMP1 in LCLs, we cloned wild-type LMP1 into a doxycycline double-inducible episomal vector pRT-1, with a truncated version of NGFR as a surrogate marker of inducibility. We found that LMP1 overexpression induced apoptosis in LCL B cells, as shown by annexin V labeling, sub-G(1) peak, and poly(ADP ribose) polymerase cleavage. Knocking down Fas expression by small interfering RNA abolished LMP1-induced apoptosis. The absence of detectable levels of Fas ligand mRNA suggested a ligand-independent activation of Fas. LMP1 induced Fas overexpression with its relocalization in lipid raft microdomains of the membrane. Fas immunoprecipitation detected FADD (Fas-associated death domain protein) and caspase 8, suggesting a Fas-dependent formation of the death-inducing signaling complex. Caspases 8, 9, 3, and 7 were activated by LMP1. Caspase 8 activation was associated with BID cleavage and truncated-BID mitochondrial relocalization, consistent with type II apoptosis. Therefore, our results are in agreement with a model where LMP1-dependent NF-kappaB activation induces Fas overexpression and autoactivation that could overwhelm the antiapoptotic effect of NF-kappaB, revealing an ambivalent function of LMP1 in cell survival and programmed cell death.
爱泼斯坦-巴尔病毒(EBV)癌蛋白潜伏膜蛋白1(LMP1)被认为是通过改变肿瘤坏死因子受体家族信号通路,在多种细胞类型中充当主要的转化蛋白。尽管LMP1在EBV相关的细胞转化中具有上述作用,但其毒性却是一个众所周知但研究较少的特性,这可能是因为它与其在转化中的作用相矛盾。我们发现LMP1的生理水平非常不均一,并且LMP1的最高水平与淋巴母细胞系(LCLs)中Fas的过表达和自发凋亡相关。为了了解LMP1在LCLs中的细胞毒性作用,我们将野生型LMP1克隆到一个强力霉素双诱导附加型载体pRT-1中,用截短的NGFR作为诱导性的替代标记。我们发现LMP1的过表达诱导LCL B细胞凋亡,这通过膜联蛋白V标记、亚G1峰和聚(ADP核糖)聚合酶裂解得以证明。通过小干扰RNA敲低Fas表达可消除LMP1诱导的凋亡。未检测到Fas配体mRNA水平,提示Fas的配体非依赖性激活。LMP1诱导Fas过表达并使其重新定位到膜的脂筏微区。Fas免疫沉淀检测到FADD(Fas相关死亡结构域蛋白)和半胱天冬酶8,提示死亡诱导信号复合物的Fas依赖性形成。半胱天冬酶8、9、3和7被LMP1激活。半胱天冬酶8的激活与BID裂解和截短的BID向线粒体的重新定位相关,这与II型凋亡一致。因此,我们的结果与一个模型相符,即LMP1依赖性的NF-κB激活诱导Fas过表达和自激活,这可能会压倒NF-κB的抗凋亡作用,揭示了LMP1在细胞存活和程序性细胞死亡中的矛盾功能。