Borgulya P, Kishi H, Uematsu Y, von Boehmer H
Basel Institute for Immunology, Switzerland.
Cell. 1992 May 1;69(3):529-37. doi: 10.1016/0092-8674(92)90453-j.
Exclusion and inclusion of T cell receptor (TCR) genes were analyzed in alpha beta TCR transgenic mice. Both transgenes are expressed unusually early on the surface of CD4-8-, HSA+, IL-2R- thymocytes. These progenitor cells give rise to progeny, which at the single-cell level contains endogenous alpha but not beta TCR-RNA as well as protein, in addition to products encoded by the transgenes. Thus, the surface expression of an alpha beta TCR does not prevent further alpha TCR rearrangement in immature thymocytes that still transcribe RAG-1 and RAG-2 genes. Reduced levels of RAG-1 and RAG-2 RNA are detectable only in CD4+8+ TCR high cells, which result from positive selection in the thymus. The results suggest that a developing T cell may try different alpha beta TCRs for binding to thymic MHC ligands, and that recombination at the alpha locus ceases only after positive selection.
在αβT细胞受体(TCR)转基因小鼠中分析了T细胞受体(TCR)基因的排除和重排情况。两种转基因均在CD4 - 8 -、HSA +、IL - 2R - 胸腺细胞表面异常早期表达。这些祖细胞产生的子代细胞,在单细胞水平上,除了转基因编码的产物外,还含有内源性α但不含有βTCR - RNA以及蛋白质。因此,αβTCR的表面表达并不阻止仍转录RAG - 1和RAG - 2基因的未成熟胸腺细胞中进一步的αTCR重排。只有在胸腺中经过阳性选择产生的CD4 + 8 + TCR高表达细胞中才能检测到RAG - 1和RAG - 2 RNA水平的降低。结果表明,正在发育的T细胞可能会尝试不同的αβTCR与胸腺MHC配体结合,并且α基因座的重组仅在阳性选择后才停止。