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褐云玛瑙螺肿瘤坏死因子α抑制褐云玛瑙螺肝细胞内乙型肝炎病毒复制。

Suppression of hepatitis B virus replication in Tupaia hepatocytes by tumor necrosis factor alpha of Tupaia belangeri.

机构信息

Department of Microbiology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.

出版信息

Comp Immunol Microbiol Infect Dis. 2011 Jul;34(4):361-8. doi: 10.1016/j.cimid.2011.05.003. Epub 2011 Jun 28.

Abstract

Recently, Tupaia belangeri was used to study the full replication cycle of hepatitis B virus (HBV) in the primary hepatocyte cultures. Thus, the Tupaia model represents a suitable model to study the effects of cytokines on HBV infection. Here, Tupaia tumor necrosis factor-alpha (TNF-α) was molecularly cloned and expressed in mammalian cells. A test system for the biological activity of Tupaia TNF-α was established on the basis of its cytotoxic effect to the murine fibrosarcoma cell line L929. Recombinant Tupaia TNF-α was able to suppress HBV replication in primary Tupaia hepatocytes (PTH). However, the formation of HBV covalently closed circular DNA (cccDNA) and viral RNA was not completely prevented. Therefore, Tupaia TNF-α may contribute significantly to the control of HBV infection though it is not able to completely inhibit HBV replication alone. The characterization of this important cytokine allows further studies on its antiviral actions in the Tupaia model.

摘要

最近,已使用树鼩来研究乙型肝炎病毒(HBV)在原代肝细胞培养物中的完整复制周期。因此,树鼩模型代表了研究细胞因子对 HBV 感染影响的合适模型。在这里,已对树鼩肿瘤坏死因子-α(TNF-α)进行了分子克隆和在哺乳动物细胞中的表达。基于其对鼠纤维肉瘤细胞系 L929 的细胞毒性作用,建立了检测树鼩 TNF-α 生物学活性的测试系统。重组树鼩 TNF-α能够抑制原代树鼩肝细胞(PTH)中的 HBV 复制。然而,HBV 共价闭合环状 DNA(cccDNA)和病毒 RNA 的形成并未完全被阻止。因此,尽管树鼩 TNF-α单独使用时不能完全抑制 HBV 复制,但它可能会显著有助于控制 HBV 感染。对这种重要细胞因子的特性进行研究,可进一步研究其在树鼩模型中的抗病毒作用。

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