Adenovirus E3 Proteins: 14.7K, RID, and gp19K Inhibit Immune-Induced Cell Death; Adenovirus Death Protein Promotes Cell Death

William S.M. Wold , Ann E. Tollefson
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引用次数: 23

Abstract

The adenovirus E3 transcription unit encodes proteins named E3-14.7K, RID, and E3-gp19K that prevent killing of infected cells by the host immune system. Tumor necrosis factor (TNF), a cytokine secreted by activated monocytes and cytotoxic T lymphocytes (CTL), can induce apoptosis when it engages the TNF receptor on target cells. E3-14.7K and RID independently prevent TNF-induced apoptosis. Fas ligand, which is expressed on activated CTL and natural killer cells, induces apoptosis when it engages its receptor, Fas, on target cells. RID blocks apoptosis through Fas by stimulating the clearance of Fas from the infected cell surface and its degradation in lysosomes. CTL induce apoptosis when the T cell receptor engages the MHC class I antigen–peptide complex on target cells. E3-gp19K inhibits killing by CTL by blocking transport of MHC class I antigens to the infected cell surface. After virus replication is complete, the cell lyses and releases virus particles; this cell lysis is mediated by the E3-coded adenovirus death protein.

腺病毒E3蛋白:14.7K、RID和gp19K抑制免疫诱导的细胞死亡腺病毒死亡蛋白促进细胞死亡
腺病毒E3转录单位编码名为E3-14.7 k、RID和E3- gp19k的蛋白质,这些蛋白质可以防止宿主免疫系统杀死受感染的细胞。肿瘤坏死因子(TNF)是一种由活化单核细胞和细胞毒性T淋巴细胞(CTL)分泌的细胞因子,当它与靶细胞上的TNF受体结合时,可以诱导细胞凋亡。E3-14.7K和RID单独阻止tnf诱导的细胞凋亡。Fas配体在活化的CTL和自然杀伤细胞上表达,当其与靶细胞上的受体Fas结合时,可诱导细胞凋亡。RID通过刺激Fas从感染细胞表面清除并在溶酶体中降解来阻止Fas凋亡。当T细胞受体与靶细胞上的MHC I类抗原肽复合物结合时,CTL诱导细胞凋亡。E3-gp19K通过阻断MHC I类抗原向感染细胞表面的转运来抑制CTL杀伤。病毒复制完成后,细胞裂解并释放病毒颗粒;这种细胞裂解是由e3编码的腺病毒死亡蛋白介导的。
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