Zink M C, Narayan O
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Virol. 1989 Jun;63(6):2578-84. doi: 10.1128/JVI.63.6.2578-2584.1989.
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.
在本研究中,我们调查了慢病毒诱导的干扰素(LV-IFN)对山羊关节炎-脑炎病毒与其宿主细胞单核细胞-巨噬细胞相互作用的影响。将新鲜山羊淋巴细胞添加到感染山羊关节炎-脑炎病毒的山羊巨噬细胞中48小时后,在培养上清液中产生了LV-IFN。通过抑制水泡性口炎病毒诱导的成纤维细胞裂解测定,培养上清液中IFN活性的效价为1:360。LV-IFN抑制体外单核细胞增殖以及单核细胞向巨噬细胞的成熟。然而,经处理的单核细胞产生前列腺素E2,这是一种通常由活化巨噬细胞产生的细胞因子。通过抑制单核细胞向更易感染的巨噬细胞的成熟,LV-IFN间接下调病毒复制。该细胞因子对已成熟巨噬细胞中的病毒基因表达也有直接抑制作用。在这些细胞中,LV-IFN在转录水平阻断病毒生命周期。最后,LV-IFN阻断感染的巨噬细胞与高度易感染的山羊滑膜细胞之间的融合。通过限制巨噬细胞成熟、病毒复制和细胞融合,LV-IFN可能在体内下调病毒复制的净速率。这些功能可能通过降低病毒基因组的表达而有助于病毒在宿主体内的持续存在。