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小鼠实验性克雅氏病的白质超微结构病理学

White matter ultrastructural pathology of experimental Creutzfeldt-Jakob disease in mice.

作者信息

Liberski P P, Yanagihara R, Gibbs C J, Gajdusek D C

机构信息

Laboratory of Central Nervous System Studies, National Institute of Neurological Disorders and Stroke, Bethesda, MD 20892.

出版信息

Acta Neuropathol. 1989;79(1):1-9. doi: 10.1007/BF00308949.

Abstract

Creutzfeldt-Jakob disease (CJD), previously regarded as a neurodegenerative disorder strictly of the gray matter, occasionally occurs as a panencephalopathic form which is characterized by severe white matter damage. An ultrastructural study of the white matter pathology in mice experimentally infected with the Fujisaki strain of CJD virus revealed: (1) vacuoles within myelin sheaths, formed by splitting either at the major dense or intraperiod lines, or within axons; (2) macrophages filled with numerous myelin figures, lipid droplets and paracrystalline inclusions; (3) astrocytes actively digesting myelin debris; (4) unusual wrapping of several axons by a common myelin sheath; (5) vesicular degeneration of myelin sheaths; (6) close contact between numerous coated pits and outer myelin lamellae; and (7) proliferation of inner mesaxons. Our data indicate that the damage to myelinated axons in the panencephalopathic type of CJD is accomplished primarily by active degradation of myelin by macrophages and astrocytes and by formation of intra-axonal and intra-myelin vacuoles. The myelin vacuolation is most consistent with that produced by leukolysins released from activated macrophages and astrocytes.

摘要

克雅氏病(CJD),以前被认为是一种严格局限于灰质的神经退行性疾病,偶尔会以全脑病变形式出现,其特征是严重的白质损伤。对实验感染CJD病毒藤崎株的小鼠白质病理学进行的超微结构研究显示:(1)髓鞘内的空泡,由主致密线或周期内线处的分裂形成,或在轴突内形成;(2)充满大量髓鞘样结构、脂滴和副结晶包涵体的巨噬细胞;(3)积极消化髓鞘碎片的星形胶质细胞;(4)几个轴突被共同的髓鞘异常包裹;(5)髓鞘的小泡样变性;(6)大量有被小窝与髓鞘外板紧密接触;(7)内系膜的增殖。我们的数据表明,全脑病变型CJD中髓鞘化轴突的损伤主要是由巨噬细胞和星形胶质细胞对髓鞘的主动降解以及轴突内和髓鞘内空泡的形成所致。髓鞘空泡化与活化巨噬细胞和星形胶质细胞释放的溶白细胞素产生的空泡化最为一致。

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