van Ewijk W, Ron Y, Monaco J, Kappler J, Marrack P, Le Meur M, Gerlinger P, Durand B, Benoist C, Mathis D
Department of Cell Biology, Immunology and Genetics, Erasmus University, Rotterdam, The Netherlands.
Cell. 1988 May 6;53(3):357-70. doi: 10.1016/0092-8674(88)90156-0.
A set of transgenic mouse lines carrying Ek alpha genes with promoter region deletions was created in an attempt to compartmentalize MHC class II gene expression. Fine immunohistological analyses established that one transgenic line is essentially devoid of E complex in the thymic cortex, another displays almost no E in the thymic medulla or on peripheral macrophages, and two lines display no E on greater than 98% of B cells. We have assayed these mice for immune function: E-dependent tolerance, antigen presentation, T cell priming, and antibody response. Certain of the findings are difficult to reconcile with currently popular hypotheses, e.g., tolerance induction to E molecules in the virtual absence of E complex in the thymic medulla and efficient antibody responses to E-restricted antigens when almost all B cells are E-.
为了区分MHC II类基因的表达,构建了一组携带启动子区域缺失的Ekα基因的转基因小鼠品系。精细的免疫组织学分析表明,一个转基因品系在胸腺皮质中基本没有E复合体,另一个在胸腺髓质或外周巨噬细胞上几乎没有E,还有两个品系在超过98%的B细胞上没有E。我们对这些小鼠的免疫功能进行了检测:E依赖的耐受性、抗原呈递、T细胞致敏和抗体反应。某些发现难以与目前流行的假说相协调,例如,在胸腺髓质中几乎没有E复合体的情况下对E分子的耐受性诱导,以及当几乎所有B细胞都是E阴性时对E限制性抗原的有效抗体反应。