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鉴定永生化中脑细胞系 CSM14.1 中的日本脑炎病毒感染。

Characterization of Japanese encephalitis virus infection in an immortalized mesencephalic cell line, CSM14.1.

机构信息

Division of Molecular Pathobiology, Hokkaido University Research Center for Zoonosis Control, West 10 North 20, Kita-ku, Sapporo, 001-0020, Japan.

出版信息

Microbiol Immunol. 2013 Oct;57(10):723-31. doi: 10.1111/1348-0421.12085.

Abstract

Neurons are the major target cell of Japanese encephalitis virus (JEV). Rats intracerebrally inoculated with JEV show an age-dependent pattern of resistance to infection in which resistance is closely associated with neuronal maturation. However, because there is no reliable and convenient cell culture system that mimics the in vivo properties of JEV infection of immature and mature neurons, the mechanisms underlying this association remain poorly understood. The aim of the present study was to examine JEV infection in immortalized CSM14.1 rat neuronal cells, which can be induced to differentiate into neurons by culture under non-permissive conditions. JEV infected undifferentiated CSM14.1 cells more efficiently than differentiated cells, resulting in production of more progeny virus in the former setting than in the latter. An infectious virus recovery assay detected more internalized virions in undifferentiated cells. On the other hand, JEV infection of differentiated cells induced more rapid and stronger expression of interferon-β gene, along with smaller amounts of JEV RNA. Taken together, these results show that the initial phase of viral infection and the later IFN response play roles in the viral susceptibility of undifferentiated and differentiated CSM14.1 cells. Because CSM14.1 cells became more resistant to JEV infection as they mature, this culture system can be used as an in vitro model for studying age-dependent resistance of neurons to JEV infection.

摘要

神经元是日本脑炎病毒(JEV)的主要靶细胞。用 JEV 脑内接种大鼠显示出感染的年龄依赖性抗性模式,其中抗性与神经元成熟密切相关。然而,由于没有可靠和方便的细胞培养系统可以模拟 JEV 感染不成熟和成熟神经元的体内特性,因此这种关联的机制仍知之甚少。本研究的目的是研究永生的 CSM14.1 大鼠神经元细胞中的 JEV 感染,这些细胞可以通过在非允许条件下培养诱导分化为神经元。JEV 感染未分化的 CSM14.1 细胞比分化细胞更有效,导致前者比后者产生更多的子代病毒。感染性病毒回收试验检测到未分化细胞中更多内化的病毒粒子。另一方面,JEV 感染分化细胞诱导干扰素-β基因更快更强的表达,同时 JEV RNA 量减少。总之,这些结果表明,病毒感染的初始阶段和随后的 IFN 反应在未分化和分化的 CSM14.1 细胞对 JEV 的易感性中起作用。由于 CSM14.1 细胞在成熟过程中对 JEV 的感染变得更具抗性,因此该培养系统可用于研究神经元对 JEV 感染的年龄依赖性抗性。

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