Moore G R, Traugott U, Raine C S
J Neurol Sci. 1984 Aug;65(2):137-45. doi: 10.1016/0022-510x(84)90078-9.
Demyelinated plaques of chronic relapsing experimental autoimmune encephalomyelitis (EAE) have been examined in Strain 13 guinea pigs. Oligodendrocytes could be identified within these lesions adjacent to naked axons and astrocytic processes. Oligodendrocytes were identified both ultrastructurally and immunocytochemically. Many of these cells showed bizarre shapes and myelin within their cytoplasm. The survival of oligodendrocytes within these lesions suggests that the myelin sheath, not the oligodendrocyte, is the primary target in autoimmune demyelination. A similar sequence of events has been proposed in multiple sclerosis, for which chronic relapsing EAE serves as a laboratory model. The persistence of myelinating cells in areas of chronic demyelination and gliosis might have significant reparatory implications.
对13系豚鼠慢性复发性实验性自身免疫性脑脊髓炎(EAE)的脱髓鞘斑块进行了检查。在这些病变中,可在裸露轴突和星形胶质细胞突起附近识别出少突胶质细胞。通过超微结构和免疫细胞化学方法鉴定了少突胶质细胞。许多这些细胞呈现出怪异的形状,并且其细胞质内有髓磷脂。这些病变中少突胶质细胞的存活表明,在自身免疫性脱髓鞘中,髓鞘而非少突胶质细胞是主要靶点。在多发性硬化症中也提出了类似的事件序列,慢性复发性EAE可作为其实验室模型。在慢性脱髓鞘和胶质增生区域中髓鞘形成细胞的持续存在可能具有重要的修复意义。