登革病毒 NS1 会导致肝细胞中 HNF4 alpha 的下调,从而导致凝血因子 I、V、X 和 XIII 的减少,造成凝血功能障碍。

IF 4 2区 医学 Q2 VIROLOGY
Sandeepan Das, Md Hasan Mallik, Partha Chattopadyay, Susenjit Mallick, Dibyajyoti Karmakar, Subhadip Ghora, Feroza Begum, Bilash Chatterjee, Dluya Samuel Thagriki, Amit Kumar Srivastava, Upasana Ray
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引用次数: 0

摘要

登革病毒 NS1 蛋白是一种主要的致病蛋白。在本研究中,我们研究了 NS1 在登革热感染相关凝血病中的作用,这是登革热病毒发病机制的一个共同特征。由于大多数凝血因子是由肝细胞产生的,而肝脏是感染过程中受影响的关键器官,因此我们使用从过表达 NS1 蛋白的 Huh7 细胞中提取的总 RNA 进行了转录组学研究。在所有四种血清型的登革热粘附和非粘附细胞培养系统中,凝血因子1、5、10和13都出现了下调,并通过定量实时聚合酶链反应(RT-PCR)和Western印迹检测得到了证实。我们还确定,凝血因子的下调是转录激活因子 HNF4α 表达减少的结果。此外,我们还证明细胞外信号调节激酶(ERK)的磷酸化导致 HNF4α 下调,进而导致凝血因子下调。通过在 BALB/c 小鼠尾静脉注射 NS1 表达质粒,验证了 HNF4α 的下调和随后凝血因子的下调。使用登革热患者血浆进行的 Western 印迹分析表明,在发热期,凝血级联共同通路中至少有两种凝血因子被下调,而在康复期水平有所提高。在细胞内和分泌型NS1中都观察到了NS1介导的凝血因子下调。病毒感染试验也验证了这一假设。总之,我们的研究强调了 NS1 在介导凝血病中的作用,它通过磷酸化 ERK 的升高对 HNF4α 的转录抑制来调节凝血因子的表达。这一信号级联可作为针对与病毒有关的凝血病的治疗干预目标:重要意义:血小板减少症与登革热感染的凝血功能障碍有关,患有凝血功能障碍的登革热患者通常需要输注血小板。对于没有血小板减少的凝血病症,输注血小板可能无济于事。我们证明了 NS1 通过下调凝血因子本身在凝血病中的作用。当血小板减少症不存在时,或者当血小板减少症和凝血因子水平降低是凝血病的致病因素时,仅输注血小板可能是无效的。其他策略,如给予凝血因子鸡尾酒或在输注凝血因子鸡尾酒的同时输注血小板,可能会有希望。我们的研究还发现了NS1通过磷酸化ERK和HNF4α介导的凝血因子下调信号通路。HNF4α是许多其他肝脏代谢因子和途径(如脂质代谢、碳水化合物代谢等)的转录调节因子,因此,针对基于NS1的HNF4α下调的治疗可以设计出治疗其他登革热肝功能异常的候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dengue virus NS1 leads to downregulation of HNF4 alpha in liver cells resulting in a decrease in coagulation factors I, V, X, and XIII, contributing to coagulopathy.

Dengue virus NS1 protein is a major pathogenic protein. In this study, we examined the role of NS1 in coagulopathy associated with Dengue infection, a common feature of Dengue virus pathogenesis. Since most coagulation factors are produced by hepatocytes and liver is key organ affected during infection, we conducted transcriptomics using total-RNA extracted from Huh7 cells overexpressing NS1 protein. Coagulation factors 1, 5, 10, and 13 were downregulated and was confirmed using quantitative real-time polymerase chain reaction (RT-PCR) and western blot assays in both adherent and non-adherent cell culture systems across all four serotypes of Dengue. We also determined that downregulation of coagulation factors is a result of reduced expression of transcription activator HNF4α. Furthermore, we demonstrated that phosphorylation of extracellular signal-regulated kinase (ERK) leads to HNF4α downregulation and subsequent downregulation of coagulation factors. The downregulation of HNF4α and the downregulation of subsequent coagulation factors were validated in BALB/c mice by hydrodynamic tail vein injection of NS1 expression plasmids. Western blot assays using plasma from Dengue patients indicated that at least two coagulation factors of the common pathway of coagulation cascade are downregulated during the febrile phase, with levels improving toward the convalescent phase. NS1-mediated downregulation of coagulation factors was observed for both intracellular and secreted NS1. The hypothesis was also validated using virus infection assays. Overall, our study highlights the role of NS1 in mediating coagulopathy by modulating the expression of coagulation factors through transcriptional suppression of HNF4α by elevated phosphorylated ERK. This signaling cascade could be targeted for therapeutic intervention against virus-related coagulopathies.

Importance: Thrombocytopenia has been linked to coagulopathy of Dengue infection, and Dengue patients with coagulopathies are often administered platelet transfusion. For coagulopathies without thrombocytopenia, platelet transfusion might not help. We demonstrated the role of NS1 in coagulopathy by downregulating coagulation factors themselves. When thrombocytopenia does not exist or when thrombocytopenia as well as reduced levels of coagulation factors are the causative factors for coagulopathies, only platelet transfusion might not be effective. Alternative strategies, like administration of coagulation factor cocktails or platelet transfusion along with coagulation factor cocktail, might be promising. Our work also leads to a signaling pathway of NS1-mediated downregulation of coagulation factors via phosphorylated ERK and HNF4α. HNF4α is a transcription regulator for many other liver-based metabolic factors and pathways like lipid metabolism, carbohydrate metabolism, etc, and thus, therapeutic targeting of NS1-based downregulation of HNF4α can lead to designing therapeutic candidates for managing other Dengue-based liver dysfunction.

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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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