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人类细胞中干扰素诱导的Mx A基因表达的调控

Control of IFN-inducible MxA gene expression in human cells.

作者信息

Ronni T, Melén K, Malygin A, Julkunen I

机构信息

Molecular Biology Programme, National Public Health Institute, Helsinki, Finland.

出版信息

J Immunol. 1993 Mar 1;150(5):1715-26.

PMID:7679692
Abstract

MxA is an IFN-induced human protein which is located in the cytoplasm of induced cells. MxA makes the cells resistant to infection by influenza and vesicular stomatitis viruses. In the present work we used baculovirus expression system to produce MxA protein. The protein was purified to homogeneity and highly specific polyclonal anti-MxA antibodies were prepared. In human mononuclear cells, and A549 lung carcinoma cells expression of MxA protein is induced by very low (< 1 IU/ml) doses of leukocyte IFN-alpha (nIFN-alpha), whereas IFN-gamma does not seem to induce it or potentiate the induction by IFN-alpha. In mononuclear cells stimulated with high doses of leukocyte IFN-alpha concentrations, the amount of MxA mRNA was induced 10-fold at 4 h after IFN induction and up to 10-fold higher MxA protein levels were observed at 24-48 h postinduction. The gene can be reinduced by IFN-alpha 24 h after the initial induction suggesting for a lack of negative feedback after this time point. The protein is very stable, the half-life being approximately 2.3 days. Flow cytometric analysis revealed that monocytes have higher basal and induced MxA protein levels than lymphocytes but the dose-dependency of MxA expression is very similar in both cell types. Granulocytes are producing very low amounts of MxA protein.

摘要

Mx蛋白是一种干扰素诱导的人类蛋白,位于被诱导细胞的细胞质中。Mx蛋白使细胞对流感病毒和水疱性口炎病毒的感染具有抗性。在本研究中,我们使用杆状病毒表达系统来生产Mx蛋白。该蛋白被纯化至同质,并制备了高度特异性的抗Mx蛋白多克隆抗体。在人单核细胞和A549肺癌细胞中,极低剂量(<1 IU/ml)的白细胞干扰素-α(nIFN-α)可诱导Mx蛋白的表达,而干扰素-γ似乎不会诱导其表达或增强干扰素-α的诱导作用。在用高剂量白细胞干扰素-α刺激的单核细胞中,干扰素诱导后4小时,Mx mRNA的量增加了10倍,诱导后24 - 48小时观察到Mx蛋白水平高达10倍以上。该基因在初次诱导后24小时可被干扰素-α再次诱导,表明在此时间点之后缺乏负反馈。该蛋白非常稳定,半衰期约为2.3天。流式细胞术分析显示,单核细胞的基础和诱导型Mx蛋白水平高于淋巴细胞,但两种细胞类型中Mx蛋白表达的剂量依赖性非常相似。粒细胞产生的Mx蛋白量非常低。

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