Department of Dermatology, Universitätsklinikum Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg, Hartmannstr. 14, 91054 Erlangen, Germany.
Department of Virology, University of Helsinki, PO Box 21, Haartmaninkatu 3, 00014, Finland.
EBioMedicine. 2018 Feb;28:151-161. doi: 10.1016/j.ebiom.2018.01.004. Epub 2018 Jan 4.
HIV-Nef activates the myeloid cell-typical tyrosine kinase Hck, but its molecular role in the viral life cycle is not entirely understood. We found that HIV plasma extracellular vesicles (HIV pEV) containing/10 proteases and Nef also harbor Hck, and analyzed its role in the context of HIV pEV secretion. Myeloid cells required Hck for the vesicle-associated release of ADAM17. This could be induced by the introduction of Nef and implied that HIV targeted Hck for vesicle-associated ADAM17 secretion from a myeloid compartment. The other contents of HIV-pEV, however, including miRNA and effector protein profiles, as well as the presence of haptoglobin suggested hepatocytes as a possible cellular source. HIV liver tissue analysis supported this assumption, revealing induction of Hck translation, evidence for ADAM protease activation and HIV infection. Our findings suggest that HIV targets Hck to induce pro-inflammatory vesicles release and identifies hepatocytes as a possible host cell compartment.
HIV-Nef 激活了髓系细胞特有的酪氨酸激酶 Hck,但它在病毒生命周期中的分子作用尚不完全清楚。我们发现含有/10 种蛋白酶和 Nef 的 HIV 血浆细胞外囊泡 (HIV pEV) 也含有 Hck,并分析了其在 HIV pEV 分泌背景下的作用。髓系细胞需要 Hck 才能将 ADAM17 与囊泡相关联释放。这可以通过引入 Nef 来诱导,这意味着 HIV 将 Hck 靶向为从髓系隔室中与囊泡相关联的 ADAM17 分泌。然而,HIV-pEV 的其他内容,包括 miRNA 和效应蛋白谱,以及触珠蛋白的存在表明肝细胞可能是潜在的细胞来源。HIV 肝组织分析支持这一假设,揭示了 Hck 翻译的诱导、ADAM 蛋白酶激活和 HIV 感染的证据。我们的研究结果表明,HIV 将 Hck 作为靶标诱导促炎囊泡释放,并确定了肝细胞作为可能的宿主细胞隔室。