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慢性感染嗜神经冠状病毒的小鼠脊髓中星形胶质细胞的激活。

Activation of astrocytes in the spinal cord of mice chronically infected with a neurotropic coronavirus.

作者信息

Sun N, Grzybicki D, Castro R F, Murphy S, Perlman S

机构信息

Department of Pediatrics, University of Iowa, Iowa City 52242, USA.

出版信息

Virology. 1995 Nov 10;213(2):482-93. doi: 10.1006/viro.1995.0021.

Abstract

Mice infected with the neurotropic JHM strain of mouse hepatitis virus (MHV-JHM) develop a demyelinating encephalomyelitis several weeks after infection. Astrogliosis and infiltration of inflammatory cells are prominent findings in the brains and spinal cords of infected mice. In this report, astrocytes in infected spinal cords were analyzed for expression of three pleiotropic cytokines, TNF-alpha, IL-1 beta, and IL-6; Type 2 nitric oxide synthase (iNOS); and MHC class I and II antigen. The data show that all three cytokines and iNOS are expressed by astrocytes in chronically infected spinal cords. These activated astrocytes are localized to areas of virus infection and demyelination, although most of the astrocytes expressing these proteins are not MHV-infected. MHC class I and II antigen can be detected in these spinal cords as well, but not in cells with the typical morphology of astrocytes. TNF-alpha, IL-6, and iNOS are also evident in the brains of mice with MHV-induced acute encephalitis, but in marked contrast to the results obtained with the chronically infected mice, most of the cells expressing these cytokines or iNOS had the morphology of macrophages or other mononuclear cells and very few appeared to be astrocytes. Additionally, astrocytes and, most likely, oligodendrocytes are infected in the spinal cords of mice with chronic demyelination. These results are consistent with a role for both viral infection of glial cells and high localized levels of proinflammatory cytokines and nitric oxide in the demyelinating process in mice infected with MHV-JHM. They also show that analogously to the human demyelinating disease, multiple sclerosis, astrocytes are a major cellular source for these cytokines in mice with chronic, but not acute disease.

摘要

感染嗜神经小鼠肝炎病毒(MHV-JHM)株的小鼠在感染数周后会发生脱髓鞘性脑脊髓炎。星形胶质细胞增生和炎性细胞浸润是感染小鼠脑和脊髓中的突出表现。在本报告中,对感染脊髓中的星形胶质细胞进行了分析,检测了三种多效性细胞因子TNF-α、IL-1β和IL-6、2型一氧化氮合酶(iNOS)以及MHC I类和II类抗原的表达。数据显示,在慢性感染的脊髓中,所有这三种细胞因子和iNOS均由星形胶质细胞表达。这些活化的星形胶质细胞定位于病毒感染和脱髓鞘区域,尽管大多数表达这些蛋白的星形胶质细胞并未被MHV感染。在这些脊髓中也可检测到MHC I类和II类抗原,但在具有典型星形胶质细胞形态的细胞中未检测到。TNF-α、IL-6和iNOS在MHV诱导的急性脑炎小鼠的脑中也很明显,但与慢性感染小鼠的结果形成鲜明对比的是,大多数表达这些细胞因子或iNOS的细胞具有巨噬细胞或其他单核细胞的形态,很少有细胞看起来是星形胶质细胞。此外,在患有慢性脱髓鞘的小鼠脊髓中,星形胶质细胞以及很可能还有少突胶质细胞被感染。这些结果与胶质细胞的病毒感染以及促炎细胞因子和一氧化氮的高局部水平在感染MHV-JHM的小鼠脱髓鞘过程中的作用一致。它们还表明,与人类脱髓鞘疾病多发性硬化症类似,在患有慢性而非急性疾病的小鼠中,星形胶质细胞是这些细胞因子的主要细胞来源。

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