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NS1蛋白在体外诱导微血管内皮通透性。

NS1 Protein Induces Microvascular Endothelial Permeability In Vitro.

作者信息

Kravchuk Bogdana I, Matveev Andrey L, Kechin Andrey A, Stepanova Alena O, Emelyanova Lyudmila A, Khachatryan Sargis M, Tikunova Nina V, Khlusevich Yana A

机构信息

Institute of Chemical Biology and Fundamental Medicine Siberian Branch of Russian Academy of Sciences, 630090 Novosibirsk, Russia.

State Budgetary Healthcare Institution of the Novosibirsk Region "State Novosibirsk Regional Clinical Hospital", 630087 Novosibirsk, Russia.

出版信息

Viruses. 2025 Jun 28;17(7):923. doi: 10.3390/v17070923.

Abstract

(Omsk hemorrhagic fever virus, OHFV) is a tick-borne flavivirus that causes Omsk hemorrhagic fever (OHF), a severe zoonotic disease endemic to Western Siberia. Despite the fact that the role of NS1 proteins of various mosquito-borne flaviviruses in pathogenesis was investigated and their ability to affect human endothelial permeability was shown, the role of the NS1 protein of OHFV in pathogenesis is unstudied. In this work, the ability of OHFV NS1 to induce human endothelial permeability was investigated for the first time. It was shown that recombinant OHFV NS1 produced in eucaryotic cells directly affects both human lung microvascular endothelial cells (HLMVEC) and human umbilical vein endothelial cells (HUVEC) in vitro. RNAseq of endothelial cells treated with OHFV NS1 indicated that OHFV NS1 enhances the expression of genes associated with cellular stress responses, vascular signaling, and cell-cell junction regulation, resulting in a nonspecific increase in the endothelial permeability of various vessels. These results suggest that the NS1 protein may contribute to OHFV pathogenesis by disrupting endothelial barrier function and promoting vascular leakage, potentially playing a role in the hemorrhagic manifestations of Omsk hemorrhagic fever.

摘要

鄂木斯克出血热病毒(OHFV)是一种蜱传黄病毒,可引起鄂木斯克出血热(OHF),这是一种在西西伯利亚流行的严重人畜共患病。尽管已对多种蚊传黄病毒的NS1蛋白在发病机制中的作用进行了研究,并证明了其影响人内皮通透性的能力,但OHFV的NS1蛋白在发病机制中的作用尚未得到研究。在这项工作中,首次研究了OHFV NS1诱导人内皮通透性的能力。结果表明,在真核细胞中产生的重组OHFV NS1在体外直接影响人肺微血管内皮细胞(HLMVEC)和人脐静脉内皮细胞(HUVEC)。用OHFV NS1处理的内皮细胞的RNA测序表明,OHFV NS1增强了与细胞应激反应、血管信号传导和细胞间连接调节相关的基因的表达,导致各种血管的内皮通透性非特异性增加。这些结果表明,NS1蛋白可能通过破坏内皮屏障功能和促进血管渗漏而导致OHFV发病机制,可能在鄂木斯克出血热的出血表现中起作用。

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