Linder E
Clin Exp Immunol. 1977 Mar;27(3):531-7.
Erythrocyte autoantibodies in NZB mice react by hemagglutination methods with exposed and hidden red cell antigens. The hidden antigens can be exposed by treatment with proteolytic enzymes. By indirect immunofluorescence one antibody population can be shown to react with modified red cells. In the present study the location of the corresponding autoantigen within the membrane was studied. Mechanical or hypotonic lysis of the red cells exposed the antigen. Proteolytic digestion known to expose other erythrocyte autoantigens had no effect. The autoantigen was exposed on 'inside out' erythrocyte membrane vesicles, but not on 'right-side out' vesicles, prepared from isolated erythrocyte ghosts. Frezzing and thawing as well as mechanical disintergration of red cells liberated antigenically active material as saline-insuluble fibrillar material. The observations indicate that the autoantigen studied is located at the inner aspect of the erythrocyte membrane and suggest that it is associated with fibril-forming structural components. The observed reactivity distinguishes the described antibodies from previously identified erythrocyte autoantibodies.
NZB小鼠中的红细胞自身抗体通过血凝方法与暴露的和隐藏的红细胞抗原发生反应。隐藏的抗原可用蛋白水解酶处理使其暴露。通过间接免疫荧光可显示一个抗体群体与经修饰的红细胞发生反应。在本研究中,对相应自身抗原在膜内的定位进行了研究。红细胞的机械性或低渗裂解可使抗原暴露。已知能暴露其他红细胞自身抗原的蛋白水解消化对此没有影响。自身抗原在由分离的红细胞血影制备的“外翻”红细胞膜囊泡上暴露,但在“正位”囊泡上不暴露。红细胞的冻融以及机械破碎会释放出具有抗原活性的物质,呈盐水不溶性纤维状物质。这些观察结果表明所研究的自身抗原位于红细胞膜的内侧,并提示它与形成纤维的结构成分相关。观察到的反应性将所描述的抗体与先前鉴定的红细胞自身抗体区分开来。