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Dengue virus infection of SK Hep1 cells: inhibition of in vitro angiogenesis and altered cytomorphology by expressed viral envelope glycoprotein.

机译:SK Hep1细胞的登革热病毒感染:通过表达的病毒包膜糖蛋白抑制体外血管生成并改变细胞形态。

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Dengue virus (DENV) infection of human endothelial cells has been implicated in the pathobiology of dengue hemorrhagic fever and dengue shock syndrome. However, the mechanisms by which DENV infections alter the functional physiology of endothelial cells remain incompletely understood. In the present study, we examined the susceptibility of a human liver sinusoidal endothelial cell line SK Hep1 to all four serotypes of DENV and studied the effect of the virus on in vitro angiogenesis. All four serotypes of DENV could infect the SK Hep1 cells, but showed variable cytopathic effects, the most pronounced being that of DENV-2. Electron microscopy of the infected cells showed significant ultrastructural changes. In vitro angiogenesis assays on DENV-2 exposed SK Hep1 cells in the matrigel system showed inhibition compared with the controls. Importantly, transfection and transient expression of the DENV-2 envelope glycoprotein (E) in these cells showed drastic alterations in cell shapes and the E protein could be localized by fluorescence microscopy in terminal knob-like structures. Therefore, SK Hep1, a human hepatic sinusoid-derived endothelial cell line, may constitute a potential model to study DENV-endothelial cell interactions in vitro, especially towards understanding the possible virus-induced changes in hepatic endothelium and its role in disease pathogenesis.
机译:人类内皮细胞的登革热病毒(DENV)感染与登革出血热和登革热休克综合征的病理生物学有关。但是,DENV感染改变内皮细胞功能生理的机制仍不完全清楚。在本研究中,我们检查了人肝窦状内皮细胞系SK Hep1对DENV的所有四种血清型的敏感性,并研究了病毒对体外血管生成的影响。 DENV的所有四种血清型均可感染SK Hep1细胞,但显示出不同的细胞病变作用,最明显的是DENV-2。感染细胞的电子显微镜显示出明显的超微结构变化。与对照组相比,在Matrigel系统中暴露于DENV-2的SK Hep1细胞的体外血管生成试验显示出抑制作用。重要的是,DENV-2包膜糖蛋白(E)在这些细胞中的转染和瞬时表达显示出细胞形状的急剧变化,并且E蛋白可以通过荧光显微镜定位在末端纽结状结构中。因此,SK Hep1是人类肝正弦波衍生的内皮细胞系,可能构成研究DENV-内皮细胞相互作用的潜在模型,特别是在了解病毒诱导的肝内皮细胞变化及其在疾病发病机理中的作用。

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