首页> 外文期刊>Acta Virologica: International Journal >Transmissible gastroenteritis virus nsp7 protein localized in the cytoplasm down-regulates interleukin 8 expression in porcine intestinal epithelial cell
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Transmissible gastroenteritis virus nsp7 protein localized in the cytoplasm down-regulates interleukin 8 expression in porcine intestinal epithelial cell

机译:传染性胃肠炎病毒NSP7蛋白在细胞质中定位下调猪肠上皮细胞中白细胞介素8表达

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摘要

Transmissible gastroenteritis virus (TGEV) is an important pathogen in swine that is responsible for substantial economic losses. Previous studies suggest that the TGEV non-structural protein 7 (nsp7) plays an important role in the viral assembly process. However, the subcellular localization and other functions of the TGEV nsp7 protein are still unclear. In this study we have examined the subcellular localization and other functions of TGEV nsp7 protein through analysis of its effects on cell growth, cell cycle progression, interleukin 8 (IL-8) expression, and NF-kappa B activation. Our results showed that the nsp7 protein is localized in the cytoplasm and has no effect on intestinal epithelial cells (IECs) growth, cell cycle, and cyclin A expression. Further studies showed that TGEV nsp7 protein had no effect on GRP78 expression, could not induce endoplasmic reticulum (ER) stress and activate NF-kappa B activity. Interestingly, the IECs expressing nsp7 protein secreted lower levels of IL-8 than control cells. This is the first report to demonstrate the subcellular localization and novel functions of TGEV nsp7 protein. These findings provide novel information about the function of the poorly characterized TGEV non-structural protein 7.
机译:传染性胃肠炎病毒(TGEV)是猪的重要病原体,其负责大量经济损失。以前的研究表明,TGEv非结构蛋白7(NSP7)在病毒组装过程中起重要作用。然而,亚细胞定位和TGEv NSP7蛋白的其他功能仍然不清楚。在该研究中,我们通过分析其对细胞生长,细胞周期进展,白细胞介素8(IL-8)表达和NF-Kappa活化的影响,研究了TGEv NSP7蛋白的亚细胞定位和其他功能。我们的研究结果表明,NSP7蛋白质在细胞质中局部化,对肠上皮细胞(IECS)生长,细胞周期和细胞周期表达没有影响。进一步的研究表明,TGEV NSP7蛋白对GRP78表达没有影响,不能诱导内质网(ER)应激并激活NF-Kappa B活性。有趣的是,表达NSP7蛋白的IECs分泌的IL-8水平低于对照细胞。这是第一份证明TGEv NSP7蛋白的亚细胞定位和新功能的报告。这些发现提供了有关TGEV非结构蛋白7差的功能的新颖的信息。

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