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持续性小鼠肝炎病毒感染对小鼠星形胶质细胞中主要组织相容性复合体I类分子表达的影响。

Effect of persistent mouse hepatitis virus infection on MHC class I expression in murine astrocytes.

作者信息

Correale J, Li S, Weiner L P, Gilmore W

机构信息

Department of Neurology, USC School of Medicine, Los Angeles 90033.

出版信息

J Neurosci Res. 1995 Jan 1;40(1):10-21. doi: 10.1002/jnr.490400103.

Abstract

Neurotropic strains of mouse hepatitis virus (MHV) have been used extensively for the study of viral pathogenesis in the central nervous system (CNS), serving as models for human neurological diseases such as multiple sclerosis (MS). MHV strains A59 and JHMV both cause acute and chronic encephalomyelitis and demyelination in susceptible strains of mice and rats. In acute disease, CNS damage is most likely the result of lytic infection in neurons and oligodendrocytes, and death can be prevented by the adoptive transfer of Class I-restricted CD8+ T cells. However, in later stages of the disease induced by some MHV strains, virus tends to be restricted to astrocytes in a nonlytic infection, and the immune response appears to contribute to CNS damage. These data lead us to suggest that the astrocyte may play a central role in the neuropathogenesis of MHV infection. Consistent with this possibility, A59 has been reported to induce the expression of Class I molecules of the major histocompatibility complex (MHC) in glial cells following infection in vivo and in vitro. In this communication, we have examined the influence of persistent infection by both A59 and JHMV on MHC Class I expression in primary murine astrocytes. Persistence was characterized by the presence of intracellular viral antigen and mRNA in the absence of detectable infectious virus particles. Under these conditions, JHMV, but not A59, inhibited constitutive expression of the H-2 Kb molecule, with the magnitude of inhibition increasing with postinfection time. A59 was not able to induce Class I during persistence, presumably due to the lack of infectious virus particles. Class I expression was restored by the addition of gamma-interferon (IFN-gamma) to astrocytes persistently infected with either A59 or JHMV. Thus, Class I inhibition is not a permanent consequence of JHMV persistence, and persistence does not interfere with normal signalling pathways for Class I induction.

摘要

小鼠肝炎病毒(MHV)的嗜神经毒株已被广泛用于研究中枢神经系统(CNS)中的病毒发病机制,作为人类神经系统疾病如多发性硬化症(MS)的模型。MHV毒株A59和JHMV均可在易感的小鼠和大鼠品系中引起急性和慢性脑脊髓炎及脱髓鞘。在急性疾病中,CNS损伤很可能是神经元和少突胶质细胞中溶细胞性感染的结果,通过I类限制性CD8 + T细胞的过继转移可预防死亡。然而,在某些MHV毒株诱导的疾病后期,病毒倾向于在非溶细胞性感染中局限于星形胶质细胞,并且免疫反应似乎导致CNS损伤。这些数据使我们认为星形胶质细胞可能在MHV感染的神经发病机制中起核心作用。与此可能性一致,据报道A59在体内和体外感染后可诱导神经胶质细胞中主要组织相容性复合体(MHC)I类分子的表达。在本通讯中,我们研究了A59和JHMV持续感染对原代小鼠星形胶质细胞中MHC I类表达的影响。持续性的特征是在没有可检测到的感染性病毒颗粒的情况下存在细胞内病毒抗原和mRNA。在这些条件下,JHMV而非A59抑制H-2 Kb分子的组成型表达,抑制程度随感染后时间增加。A59在持续感染期间无法诱导I类表达,可能是由于缺乏感染性病毒颗粒。通过向持续感染A59或JHMV的星形胶质细胞中添加γ干扰素(IFN-γ)可恢复I类表达。因此,I类抑制不是JHMV持续感染的永久后果,并且持续感染不会干扰I类诱导的正常信号通路。

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