Schut R L, Gekker G, Hu S, Chao C C, Pomeroy C, Jordan M C, Peterson P K
Dept. of Medicine, Hennepin County Medical Center, Minneapolis, MN 55415.
J Infect Dis. 1994 May;169(5):1092-6. doi: 10.1093/infdis/169.5.1092.
The pathogenesis of encephalitis due to cytomegalovirus (CMV), particularly the role of microglial cells in the spread or control of infection, remains incompletely defined. In this study, microglial cells were isolated from the brains of newborn mice and infected in vitro with murine CMV (MCMV). Microglial cells supported productive MCMV replication, and the MCMV-infected microglia manifested a cytopathic effect (CPE) characteristic of CMV infection. Exposure of microglia to interferon-gamma (IFN-gamma) 24 h before infection markedly suppressed virus production and resultant CPE in a dose-dependent fashion. Furthermore, the addition of IFN-gamma 2 h after infection demonstrated an antiviral effect equivalent to that achieved when IFN-gamma was administered 2 h before infection. These results demonstrate that murine microglial cells are fully permissive to MCMV replication and that IFN-gamma markedly suppresses virus expression in these cells.
巨细胞病毒(CMV)所致脑炎的发病机制,尤其是小胶质细胞在感染传播或控制中的作用,目前仍未完全明确。在本研究中,从小鼠新生大脑中分离出小胶质细胞,并在体外用人巨细胞病毒(MCMV)进行感染。小胶质细胞支持MCMV的有效复制,且感染MCMV的小胶质细胞表现出CMV感染特有的细胞病变效应(CPE)。在感染前24小时将小胶质细胞暴露于干扰素-γ(IFN-γ),可呈剂量依赖性显著抑制病毒产生及由此产生的CPE。此外,在感染后2小时添加IFN-γ,其抗病毒效果与感染前2小时给予IFN-γ相当。这些结果表明,小鼠小胶质细胞对MCMV复制完全易感,且IFN-γ可显著抑制这些细胞中的病毒表达。