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进行性多灶性白质脑病。神经病理学与病毒分离

Progressive multifocal leukoencephalopathy. Neuropathology and virus isolation.

作者信息

Nagashima K, Yamaguchi K, Yasui K, Ogiwara H

出版信息

Acta Pathol Jpn. 1981 Nov;31(6):953-61.

PMID:6274138
Abstract

Mechanism of demyelination in progressive multifocal leukoencephalopathy (PML) was elucidated by demonstrating ultrastructurally the relationship between the affected glial cells and myelin sheaths. The myelinating cells in the central nervous system, namely oligodendroglias, were specifically attacked by PML-virus with eventual primary destruction of myelin sheaths. An attempt to isolate PML-virus from the autopsy material was made. The presence of virus particles in the extracts from the brain, reactions of virions with antibodies and evidence of virus proliferation in the primary human fetal glial cell culture were shown by various techniques including negative staining, immunofluorescence, immunoelectron microscopy, and electron micrography. The isolated virus was antigenically identical with JC type of papovaviruses.

摘要

通过超微结构显示受影响的神经胶质细胞与髓鞘之间的关系,阐明了进行性多灶性白质脑病(PML)的脱髓鞘机制。中枢神经系统中的髓鞘形成细胞,即少突胶质细胞,受到PML病毒的特异性攻击,最终导致髓鞘的原发性破坏。尝试从尸检材料中分离PML病毒。通过包括负染色、免疫荧光、免疫电子显微镜和电子显微摄影在内的各种技术,显示了脑提取物中病毒颗粒的存在、病毒粒子与抗体的反应以及病毒在原代人胎儿神经胶质细胞培养物中的增殖证据。分离出的病毒在抗原性上与乳头多瘤空泡病毒JC型相同。

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