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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >A suppressive effect of cyclosporine A on replication and noncoding control region activation of polyomavirus BK virus.
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A suppressive effect of cyclosporine A on replication and noncoding control region activation of polyomavirus BK virus.

机译:环孢素A对多马病毒BK病毒复制和非分量对照区活化的抑制作用。

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BACKGROUND: The effect of cyclosporine A (CsA) on polyomavirus BK virus (BKV) replication remains unclear. The aim of this in vitro study was to investigate the effect of CsA on BKV replication in human uroepithelial cells. METHODS: After infection of a human renal proximal tubular cell line, HK-2 with BKV, BKV viral load in the presence of CsA was assessed by real-time polymerase chain reaction. The BKV large T-antigen (LTag) expression was measured by Western blot analysis. The BKV early promoter activity was determined by measuring luciferase activity of the BKV noncoding control region luciferase reporter. The BKV LTag expression in a human bladder carcinoma cell line, T24, was assessed by immunofluorescence. RESULTS: The results demonstrated that the increased levels of BKV LTag and viral protein 1 transcripts measured by real-time polymerase chain reaction were suppressed by CsA in a dose-dependent manner (0.5-4 microg/mL). Western blot analysis also showed that CsA inhibited BKV LTag expression. In addition, the activity of the BKV early promoter, which was enhanced by BKV LTag overexpression, was abrogated by CsA. Finally, the suppressive effect of CsA on BKV replication was also shown in T24 cells as CsA reduced immunofluorescent staining of BKV LTag in these cells. CONCLUSION: This in vitro study indicates that CsA suppresses BKV replication in human proximal renal tubular cells and uroepithelial cells of the urinary bladder and inhibits the BKV-LTag-regulated increase in early promoter activity.
机译:背景:环孢素A(CSA)对多瘤BK病毒(BKV)复制的影响尚不清楚。这种体外研究的目的是探讨CSA对人类胃肠杆菌细胞BKV复制的影响。方法:在感染人肾近端管状细胞系后,用BKV的HK-2,通过实时聚合酶链反应评估CSA存在下的BKV病毒载量。通过Western印迹分析测量BKV大T-抗原(LTAG)表达。通过测量BKV非编码对照区荧光素酶报告者的荧光素酶活性来确定BKV早期启动子活性。通过免疫荧光评估人膀胱癌细胞系T24中的BKV LTAG表达T24。结果:结果表明,通过CSA以剂量依赖性方式(0.5-4 microg / ml)抑制了通过实时聚合酶链反应测量的BKV LTAG和病毒蛋白1转录物的增加水平。 Western印迹分析还表明CSA抑制了BKV LTAG表达。此外,BKV LTAG过表达增强的BKV早期启动子的活性由CSA消除。最后,CSA对BKV复制对BKV复制的抑制作用也显示为T24细胞,因为CSA在这些细胞中降低了BKV LTAG的免疫荧光染色。结论:这种体外研究表明,CSA抑制了人近端肾小管细胞中的BKV复制和尿膀胱的Uroophelial细胞,并抑制了早期启动子活性的BKV-LTAG-调节。

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