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首页> 外文期刊>Virology >Induction of Interferon-α and Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand in Human Blood Mononuclear Cells by Hemagglutinin-Neuraminidase but Not F Protein of Newcastle Disease Virus
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Induction of Interferon-α and Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand in Human Blood Mononuclear Cells by Hemagglutinin-Neuraminidase but Not F Protein of Newcastle Disease Virus

机译:血凝素-神经氨酸酶而不是新城疫病毒的F蛋白诱导人血单核细胞中干扰素-α和肿瘤坏死因子相关的凋亡诱导配体

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摘要

To determine molecular viral components which can induce innate immune responses in human peripheral blood mononuclear cells (PBMC), we investigated the anti-neoplastic agent Newcastle disease virus (NDV) and its two spike proteins hemagglutinin-neuraminidase (HN) and fusion protein (F). NDV was an excellent inducer in PBMC of IFN-α production and capable of inducing upregulation of plasma membrane expression of tumor necrosis factor related apoptosis inducing ligand (TRAIL). Viral replication was not required for these responses because NDV inactivated for 5 min by UV was as good as live NDV. NDV-modified and paraformaldehyde-fixed BHK cells could also trigger IFN-α and TRAIL induction, indicating that contacts of responder cells with NDV-modified cell surfaces are sufficient to induce these activities in PBMC. Antibodies against HN but not F were able to block these responses. Finally we could show that HN but not F induced INF-α and TRAIL in PBMC. This was possible through the use of respective gene transfectants generated with the help of Semliki Forest virus (SFV) replicase-based DNA recombinant expression systems. Upon contact with BHK cells expressing HN but not F at their cell surface, human PBMC produced IFN-α and some cells, including monocytes and T lymphocytes, upregulated cell surface TRAIL expression.
机译:为了确定可以在人外周血单个核细胞(PBMC)中诱导先天免疫应答的分子病毒成分,我们研究了抗肿瘤药新城疫病毒(NDV)及其两个刺突蛋白血凝素神经氨酸酶(HN)和融合蛋白(F )。 NDV是PBMC中IFN-α产生的极佳诱导剂,能够诱导肿瘤坏死因子相关的凋亡诱导配体(TRAIL)的质膜表达上调。这些反应不需要病毒复制,因为通过紫外线灭活5分钟的NDV与活NDV一样好。 NDV修饰和低聚甲醛固定的BHK细胞也可能触发IFN-α和TRAIL诱导,表明应答细胞与NDV修饰的细胞表面接触足以诱导PBMC中的这些活性。抗HN而非F的抗体能够阻止这些反应。最后,我们可以证明HN而非F诱导了PBMC中的INF-α和TRAIL。这可以通过使用在基于Semliki Forest病毒(SFV)复制酶的DNA重组表达系统的帮助下产生的各个基因转染子来实现。在与在其细胞表面表达HN但不表达F的BHK细胞接触后,人PBMC产生IFN-α,某些细胞(包括单核细胞和T淋巴细胞)上调了细胞表面TRAIL的表达。

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