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爱泼斯坦-巴尔病毒编码的潜伏膜蛋白1对p38丝裂原活化蛋白激酶途径的激活共同调节白细胞介素-6和白细胞介素-8的产生。

Activation of the p38 mitogen-activated protein kinase pathway by Epstein-Barr virus-encoded latent membrane protein 1 coregulates interleukin-6 and interleukin-8 production.

作者信息

Eliopoulos A G, Gallagher N J, Blake S M, Dawson C W, Young L S

机构信息

Cancer Research Campaign Institute for Cancer Studies, the University of Birmingham Medical School, Birmingham B15 2TA, United Kingdom.

出版信息

J Biol Chem. 1999 Jun 4;274(23):16085-96. doi: 10.1074/jbc.274.23.16085.

Abstract

The Epstein-Barr virus-encoded latent membrane protein 1 (LMP1) is a pleiotropic protein the activities of which include effects on gene expression and cell transformation, growth, and death. LMP1 has been shown to induce nuclear factor (NF)-kappaB and c-Jun NH2-terminal kinase/AP-1 activities in target cells, and in this study we demonstrate that LMP1 also engages the p38 mitogen-activated protein kinase cascade, leading to activation of the transcription factor ATF2. Mutational analysis of the LMP1 cytoplasmic COOH terminus revealed that p38 activation occurs from both the tumor necrosis factor receptor-associated factor (TRAF)-interacting, membrane-proximal COOH-terminal activating region (CTAR)1 domain (amino acids 186-231) and the extreme tumor necrosis factor receptor-associated death domain (TRADD) binding CTAR2 region (amino acids 351-386). Because LMP1 also engages signaling on the NF-kappaB axis through CTAR1 and CTAR2, we have examined whether these two pathways are overlapping or independent. We have found that inhibition of p38 by the highly specific inhibitor SB203580 did not affect NF-kappaB binding activity. Conversely, although the metabolic inhibitor D609 blocked NF-kappaB activation, it did not impair the ability of LMP1 to signal on the p38 axis, suggesting that these two LMP1-mediated pathways are primarily independent. Divergence of signals must, however, occur downstream of TRAF2 as a dominant negative TRAF2 mutant that blocks LMP1-induced NF-kappaB activation also inhibited p38 signaling. In addition, we have found that p38 inhibition significantly impaired LMP1-mediated interleukin-6 and -8 expression. Thus, p38 may play a significant cooperative role in regulating at least some of the pleiotropic activities of LMP1.

摘要

爱泼斯坦-巴尔病毒编码的潜伏膜蛋白1(LMP1)是一种多效性蛋白,其活性包括对基因表达、细胞转化、生长和死亡的影响。LMP1已被证明可在靶细胞中诱导核因子(NF)-κB和c-Jun NH2末端激酶/AP-1活性,在本研究中,我们证明LMP1还参与p38丝裂原活化蛋白激酶级联反应,导致转录因子ATF2的激活。对LMP1细胞质COOH末端的突变分析表明,p38激活发生在肿瘤坏死因子受体相关因子(TRAF)相互作用的膜近端COOH末端激活区域(CTAR)1结构域(氨基酸186-231)和极端肿瘤坏死因子受体相关死亡结构域(TRADD)结合CTAR2区域(氨基酸351-386)。由于LMP1还通过CTAR1和CTAR2参与NF-κB轴上的信号传导,我们研究了这两条途径是重叠还是独立的。我们发现,高特异性抑制剂SB203580对p38的抑制并不影响NF-κB结合活性。相反,尽管代谢抑制剂D609阻断了NF-κB的激活,但它并未损害LMP1在p38轴上的信号传导能力,这表明这两条LMP1介导的途径主要是独立的。然而,信号分歧一定发生在TRAF2的下游,因为一种阻断LMP1诱导的NF-κB激活的显性负性TRAF2突变体也抑制了p38信号传导。此外,我们发现p38抑制显著损害了LMP1介导的白细胞介素-6和-8的表达。因此,p38可能在调节LMP1的至少一些多效性活性中发挥重要的协同作用。

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