Kilshaw P J, Baker K C
AFRC Institute of Animal Physiology and Genetics Research, Babraham, Cambridge.
Immunology. 1989 Jun;67(2):160-6.
Rat monoclonal antibodies were prepared against intra-epithelial lymphocytes (IEL) isolated from the gut of Balb/c mice and screened for selective reactivity with mucosal lymphocytes. One antibody, M371, identified a new surface antigen on 30-40% of IEL. It bound to very few, if any, lymphocytes within the lamina propria and to none in other lymphoid tissues; neither did it stain lymph node lymphocytes that had been stimulated in culture with mitogens or alloantigens. The data suggest that M371 identifies a sessile population of IEL and that expression of the antigen is induced locally in the epithelium. In addition to IEL, M371 bound to some goblet cells in the mid and distal small gut but not in the proximal region. Double-staining experiments showed that M371 was highly specific for IEL with the phenotype Lyt-2+, Lyt-3-, Thy-1-, CD3+ and stained a majority of cells in this subpopulation. M371 precipitated a surface molecule approximately 275,000 MW in size, which was also precipitated by antibodies to CD45. Treatment of fixed IEL with sodium periodate prevented staining by M371, suggesting involvement of carbohydrate in the epitope. The specificity of M371 was shown to differ from that of the antibodies CT1 and CT2, which identify a carbohydrate determinant of CD45 expressed on cytotoxic lymphocytes and IEL. The possibility that the gut epithelium provides an environment for the functional differentiation of thymus-independent mucosal T cells is discussed.
制备了针对从Balb/c小鼠肠道分离的上皮内淋巴细胞(IEL)的大鼠单克隆抗体,并筛选其与黏膜淋巴细胞的选择性反应性。一种抗体M371在30%至40%的IEL上识别出一种新的表面抗原。它与固有层内极少的淋巴细胞(如果有的话)结合,与其他淋巴组织中的淋巴细胞无结合;它也不染色经丝裂原或同种异体抗原体外刺激的淋巴结淋巴细胞。数据表明M371识别IEL的一个固定群体,且该抗原的表达是在上皮局部诱导产生的。除IEL外,M371还与小肠中、远端的一些杯状细胞结合,但不与近端区域的杯状细胞结合。双重染色实验表明,M371对具有Lyt-2+、Lyt-3-、Thy-1-、CD3+表型的IEL具有高度特异性,并对该亚群中的大多数细胞进行染色。M371沉淀出一种大小约为275,000 MW的表面分子,该分子也可被抗CD45抗体沉淀。用高碘酸钠处理固定的IEL可阻止M371染色,提示碳水化合物参与了表位。已证明M3七的特异性与抗体CT1和CT2不同,CT1和CT2识别细胞毒性淋巴细胞和IEL上表达的CD45的碳水化合物决定簇。本文讨论了肠道上皮为非胸腺依赖性黏膜T细胞的功能分化提供环境的可能性。