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首页> 外文期刊>Journal of Leukocyte Biology: An Official Publication of the Reticuloendothelial Society >Human immunodeficiency virus type 1 (HIV-1) Nef activates STAT3 in primary human monocyte/macrophages through the release of soluble factors: involvement of Nef domains interacting with the cell endocytotic machinery
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Human immunodeficiency virus type 1 (HIV-1) Nef activates STAT3 in primary human monocyte/macrophages through the release of soluble factors: involvement of Nef domains interacting with the cell endocytotic machinery

机译:人类免疫缺陷病毒1型(HIV-1)Nef通过释放可溶性因子激活原代人单核细胞/巨噬细胞中的STAT3:Nef域与细胞内吞机制相互作用

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Increasing evidence indicates that the expression of the human immunodeficiency virus-1 (HIV-1) Nef protein significantly influences the activation state of the host cell. Here we report that Nef specifically activates STAT3 in primary human monocyte-derived macrophages (MDM). This was demonstrated by both single-cycle infection experiments driven by Vesicular Stomatitis virus glycoprotein (VSV-G) pseudotyped HIV-1 and treatment with exogenous recombinant Nef. The analysis of the effects of Nef mutants revealed that domains of the C-terminal flexible loop interacting with the cell endocytotic machinery are involved in the STAT3 activation. In particular, our data suggest that the Nef-dependent STAT3 activation relies on the targeting of Nef to the late endosome/lysosome compartment. In addition, we found that Nef activates STAT3 through a mechanism mediated by the release of soluble factor(s), including MIP-1?±, that requires de novo protein synthesis but appears independent from the activation of src tyrosine kinases. The results presented here support the idea that the first intervention of Nef in the intracellular signaling of monocyte-macrophages could generate, by means of the release of soluble factor(s), a secondary wave of activation that could be of a potential pathogenetic significance.
机译:越来越多的证据表明,人类免疫缺陷病毒1(HIV-1)Nef蛋白的表达显着影响宿主细胞的激活状态。在这里我们报告Nef专门激活人类单核细胞衍生的巨噬细胞(MDM)中的STAT3。水泡性口腔炎病毒糖蛋白(VSV-G)假型HIV-1驱动的单周期感染实验和外源重组Nef的治疗均证明了这一点。对Nef突变体影响的分析表明,与细胞内吞机制相互作用的C末端柔性环结构域与STAT3激活有关。特别是,我们的数据表明,Nef依赖性STAT3激活依赖于Nef靶向晚期内体/溶酶体区室。另外,我们发现Nef通过由可溶性因子(包括MIP-1α±)的释放介导的机制激活STAT3,所述可溶性因子需要从头合成蛋白质,但似乎不依赖于src酪氨酸激酶的激活。这里提出的结果支持这样的想法,即Nef对单核巨噬细胞的细胞内信号传导的首次干预可以通过释放可溶性因子而产生第二次激活波,这可能具有潜在的致病意义。

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