首页> 美国卫生研究院文献>Journal of Virology >Lentivirus-induced interferon inhibits maturation and proliferation of monocytes and restricts the replication of caprine arthritis-encephalitis virus.
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Lentivirus-induced interferon inhibits maturation and proliferation of monocytes and restricts the replication of caprine arthritis-encephalitis virus.

机译:慢病毒诱导的干扰素抑制单核细胞的成熟和增殖并限制山羊关节炎-脑炎病毒的复制。

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摘要

In this study, we investigated the effect of a lentivirus-induced interferon (LV-IFN) on the interaction of caprine arthritis-encephalitis virus and its host cell, the monocyte-macrophage. LV-IFN was produced in culture supernatant 48 h after adding fresh goat lymphocytes to caprine arthritis-encephalitis virus-infected goat macrophages. The culture supernatant contained IFN activity at a titer of 1:360 as assayed by inhibition of vesicular stomatitis virus-induced lysis of fibroblasts. LV-IFN inhibited in vitro monocyte proliferation and maturation of monocytes to macrophages. Nevertheless, treated monocytes produced prostaglandin E2, a cytokine generally produced by activated macrophages. By inhibiting the maturation of monocytes to the more permissive macrophage, LV-IFN indirectly downregulated virus replication. The cytokine also had a direct inhibitory effect on virus gene expression in already mature macrophages. In these cells, LV-IFN blocked the viral life cycle at the level of transcription. Finally, LV-IFN blocked fusion between infected macrophages and highly permissive goat synovial membrane cells. By restricting macrophage maturation, viral replication, and cell fusion, LV-IFN may downregulate the net rate of virus replication in vivo. These functions may contribute to the persistence of the virus in the host by reducing the expression of the viral genome.
机译:在这项研究中,我们调查了慢病毒诱导的干扰素(LV-IFN)对山羊关节炎-脑炎病毒及其宿主细胞单核巨噬细胞相互作用的影响。向山羊关节炎-脑炎病毒感染的山羊巨噬细胞中加入新鲜的山羊淋巴细胞48小时后,在培养上清液中产生LV-IFN。如通过抑制水泡性口炎病毒诱导的成纤维细胞裂解所测定的,培养物上清液以1:360的滴度包含IFN活性。 LV-IFN抑制体外单核细胞增殖和单核细胞成熟为巨噬细胞。然而,经处理的单核细胞产生前列腺素E2,前列腺素E2通常由活化的巨噬细胞产生。通过抑制单核细胞向更宽容的巨噬细胞成熟,LV-IFN间接下调了病毒复制。细胞因子对已经成熟的巨噬细胞中的病毒基因表达也具有直接的抑制作用。在这些细胞中,LV-IFN在转录水平上阻断了病毒的生命周期。最后,LV-IFN阻断了感染的巨噬细胞和高度允许的山羊滑膜细胞之间的融合。通过限制巨噬细胞的成熟,病毒复制和细胞融合,LV-IFN可能下调体内病毒复制的净速率。这些功能可通过减少病毒基因组的表达来促进病毒在宿主中的持久性。

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