Lassmann H, Ammerer H P, Kulnig W
Acta Neuropathol. 1978 Nov 15;44(2):91-102. doi: 10.1007/BF00691474.
The ultrastructural events in myelin degradation in the rat optic nerve following transection have been studied. Myelin debris was found in cells similar to multipotential glia cells (Vaughn and Peters, 1968) as well as in astrocytes and in few oligodendrocytes. The different types of inclusions found during myelin degradation were described in their quantitative relations. Similarities to inclusions described in adrenoleukodystrophy adn multiple sclerosis are discussed. By comparison of the ultrastructural findings with histochemical and biochemical data available a hypothetical model of myelin degradation is presented. The process starts with the degradation of digestible proteins resulting in uniformly layered lipid inclusions. Lipid degradation leads to the formation of unstructured lipid droplets and crystals. During the late stages of Wallerian degeneration numerous polymorph inclusion typed can be found, probably representing poorly digestible lipids or lipoproteins.
对大鼠视神经横断后髓鞘降解的超微结构变化进行了研究。在类似于多潜能神经胶质细胞(Vaughn和Peters,1968)的细胞中以及星形胶质细胞和少数少突胶质细胞中发现了髓鞘碎片。描述了髓鞘降解过程中发现的不同类型内含物的数量关系。讨论了与肾上腺脑白质营养不良和多发性硬化症中描述的内含物的相似性。通过将超微结构研究结果与现有的组织化学和生化数据进行比较,提出了一个髓鞘降解的假设模型。该过程始于可消化蛋白质的降解,导致形成均匀分层的脂质内含物。脂质降解导致形成无结构的脂质小滴和晶体。在华勒氏变性的后期,可以发现许多多形性内含物类型,可能代表难以消化的脂质或脂蛋白。