Scolding N J, Compston D A
Department of Neurology, University of Cambridge Clinical School, U.K.
Immunology. 1991 Jan;72(1):127-32.
The final pathway of myelin destruction in immune-mediated demyelination is phagocytosis by macrophages. As part of a systematic study of mechanisms of myelin-oligodendrocyte injury, we have used an in vitro approach to investigate interactions between rat oligodendrocytes and macrophages in order to identify the conditions under which macrophages adhere to and damage oligodendrocytes. No adherence was seen when macrophages alone were co-cultured with homologous oligodendrocytes. However, macrophage attachment to oligodendrocytes was triggered not only by antibody to the major cell-surface component galactocerebroside, but also by antibody to the quantitatively minor antigen, myelin-oligodendrocyte glycoprotein; immunocytochemical observations suggested that phagocytosis of myelin antigen also occurred. No such changes were seen in the presence of an irrelevant (anti-progesterone) antibody, or in the presence of activated complement. These results emphasize that a variety of antibodies, including those to minor myelin-oligodendrocyte antigens, may play a significant role in the development of demyelinated lesions.
免疫介导的脱髓鞘中髓鞘破坏的最终途径是巨噬细胞的吞噬作用。作为对髓鞘-少突胶质细胞损伤机制进行系统研究的一部分,我们采用体外方法研究大鼠少突胶质细胞与巨噬细胞之间的相互作用,以确定巨噬细胞黏附并损伤少突胶质细胞的条件。当单独将巨噬细胞与同源少突胶质细胞共培养时,未观察到黏附现象。然而,巨噬细胞与少突胶质细胞的附着不仅由针对主要细胞表面成分半乳糖脑苷脂的抗体触发,也由针对定量上较少的抗原即髓鞘-少突胶质细胞糖蛋白的抗体触发;免疫细胞化学观察表明也发生了髓鞘抗原的吞噬作用。在存在无关抗体(抗孕酮抗体)或存在活化补体的情况下未观察到此类变化。这些结果强调,包括针对髓鞘-少突胶质细胞次要抗原的抗体在内的多种抗体可能在脱髓鞘病变的发展中起重要作用。