原发性脱髓鞘持续性病毒感染的新模型。

Q4 Medicine
Neurologia-Neurocirugia Psiquiatria Pub Date : 1977-01-01
M C dal Canto, H L Lipton
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引用次数: 0

摘要

小鼠的Theiler’s encephalomyelitis virus (TMEV)是现有的几种病毒诱导脱髓鞘的动物模型之一,可能为人类疾病多发性硬化症提供进一步的信息。本超微结构研究中使用的一种近交系小鼠(SJL/j)在脑内接种TMEV后出现以深度痉挛为特征的终身神经系统疾病。在感染后7天至9个月,连续处死麻醉动物,用戊二醛全身灌注。15天后,脊髓轻脑膜和白质出现强烈的单核炎性浸润,并持续1年之久。这些浸润含有大量浆细胞,几乎每1微米的切片上都可以发现血管周围脱髓鞘。单核细胞过程中髓磷脂的囊泡和剥离被认为是髓磷脂分解的机制。然而,在灰质和白质细胞中均未发现病毒粒子,并维持了少突胶质细胞的完整性。一年后,在包含裸轴突和再髓鞘的区域仍可见活跃的脱髓鞘。这些超微结构发现与病毒诱导脱髓鞘的假设机制的相关性将被讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A new model of persistent viral infection with primary demyelination.

Theiler's encephalomyelitis virus (TMEV) in mice represents one of the few existing animal models of virus-induced demyelination and may provide further information about the human disease, Multiple Sclerosis. An inbred strain of mice (SJL/j) employed in the present ultrastructural study, develops a life-long neurologic illness characterized by profound spasticity after intracerebral inoculation of TMEV. Anesthetized animals were sacrificed sequentially by total body perfusion with gluteraldehyde from 7 days to 9 months after infection. An intense mononuclear inflammatory infiltrate appeared in the leptomeninges and white matter of spinal cord by 15 days and persisted for as long as one year. These infiltrates contained numerous plasma cells, and perivascular demyelination could be found in almost every 1 micron section. Vesiculation and stripping of myelin by mononuclear cell processes were seen as mechanisms of myelin break-down. However, virions were not found in cells in grey or white matter and the integrity of oligodendrocytes was maintained. At one year, active demyelination was still seen in areas containing naked and remyelinated axons. The relevance of these ultrastructural findings to postulated mechanisms of virus-induced demyelination will be discussed.

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来源期刊
Neurologia-Neurocirugia Psiquiatria
Neurologia-Neurocirugia Psiquiatria Psychology-Clinical Psychology
CiteScore
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