Grundke-Iqbal I, Raine C S, Johnson A B, Brosnan C F, Bornstein M B
J Neurol Sci. 1981 Apr;50(1):63-79. doi: 10.1016/0022-510x(81)90042-3.
Serum factors in rabbits with white matter-induced experimental allergic encephalomyelitis (WM-EAE) were studied with respect to their role in demyelination in vitro in organotypic central nervous system (CNS) tissue cultures and in vivo in the myelinated retina of the rabbit eye. By absorption with staphylococcal protein A, IgG was quantitatively separated from the other serum proteins. No IgG was demonstrable in the absorbed IgG-depleted sera by Ouchterlony double diffusion, immunoelectrophoresis and SDS-polyacrylamide gel electrophoresis. Both the IgG-depleted WM-EAE sera and the IgG fractions had complement-dependent demyelinating activity on CNS cultures, and both contained immunoglobulin binding to myelin and oligodendroglia of the cultures, as demonstrated by an immunoperoxidase technique. However, only the purified IgG fractions in the absence of complement induced swelling of myelin and proliferation of oligodendroglial processes with redundant myelin in tissue cultures. The IgG-depleted complement-inactivated WM-EAE sera produced no morphological changes. In the rabbit eye model, antibody-dependent cell-mediated demyelination was observed only with the IgG fractions but not with the IgG-depleted EAE sera. No oligodendroglial proliferation occurred. These studies demonstrate for the first time that in CNS cultures, non-IgG immunoglobulins as well as IgG mediate complement-dependent demyelination and that these bind to myelin and oligodendrocytes, whereas only IgG causes myelin swelling and oligodendrocyte proliferation.
对患有白质诱导实验性变应性脑脊髓炎(WM-EAE)的家兔血清因子进行了研究,以探讨其在器官型中枢神经系统(CNS)组织培养中的体外脱髓鞘作用以及在家兔眼有髓视网膜中的体内脱髓鞘作用。通过与葡萄球菌蛋白A吸附,从其他血清蛋白中定量分离出IgG。通过双向琼脂扩散、免疫电泳和SDS-聚丙烯酰胺凝胶电泳,在吸收后的IgG缺失血清中未检测到IgG。IgG缺失的WM-EAE血清和IgG组分在CNS培养物中均具有补体依赖性脱髓鞘活性,并且通过免疫过氧化物酶技术证实两者均含有与培养物中的髓鞘和少突胶质细胞结合的免疫球蛋白。然而,只有在没有补体的情况下,纯化的IgG组分才能在组织培养中诱导髓鞘肿胀和少突胶质细胞突起增殖以及多余髓鞘的形成。IgG缺失的补体失活WM-EAE血清未产生形态学变化。在家兔眼模型中,仅IgG组分观察到抗体依赖性细胞介导的脱髓鞘,而IgG缺失的EAE血清则未观察到。未发生少突胶质细胞增殖。这些研究首次证明,在CNS培养物中,非IgG免疫球蛋白以及IgG介导补体依赖性脱髓鞘,并且它们与髓鞘和少突胶质细胞结合,而只有IgG会导致髓鞘肿胀和少突胶质细胞增殖。