Oukka M, Andre P, Turmel P, Besnard N, Angevin V, Karlsson L, Trans P L, Charron D, Bihain B, Kosmatopoulos K, Lotteau V
INSERM U267, Villejuif, France.
Eur J Immunol. 1997 Apr;27(4):855-9. doi: 10.1002/eji.1830270408.
Major histocompatibility complex (MHC) restriction of the immune response is established during positive selection of T cells in the thymus. This occurs mainly through interactions of T cell receptor of developing thymocytes with MHC/peptide ligands on cortical thymic epithelial cells (TEC). An ongoing controversy concerns the origin and the role of peptides involved in the positive selection of thymocytes. Evidence provided here shows that processing of MHC class II complexes in cortical TEC differs from that of medullary TEC. Removal of the invariant chain associated with MHC class II complexes was rapid and complete in medullary TEC which present peptides from both exogenous and cytosolic origin. In cortical TEC, a large fraction of class II dimers remained associated with a 10-12-kDa fragment of invariant chain (Ii). Incomplete removal of Ii correlated with the inability of cortical TEC to present peptides from exogenous origin. However, presentation of peptides from cytosolic proteins by cortical TEC remained possible. Thus, most peptides from exogenous proteins may be excluded from participating in positive selection of CD4+ T cells by a mechanism limiting Ii breakdown.
免疫反应的主要组织相容性复合体(MHC)限制是在胸腺中T细胞的阳性选择过程中确立的。这主要通过发育中的胸腺细胞的T细胞受体与皮质胸腺上皮细胞(TEC)上的MHC/肽配体之间的相互作用而发生。一个持续存在的争议涉及参与胸腺细胞阳性选择的肽的来源和作用。此处提供的证据表明,皮质TEC中MHC II类复合体的加工与髓质TEC不同。与MHC II类复合体相关的恒定链在髓质TEC中迅速且完全去除,髓质TEC呈递来自外源性和胞质来源的肽。在皮质TEC中,很大一部分II类二聚体仍与恒定链(Ii)的10 - 12 kDa片段相关联。Ii的不完全去除与皮质TEC无法呈递外源性来源肽的能力相关。然而,皮质TEC呈递来自胞质蛋白的肽仍然是可能的。因此,通过限制Ii降解的机制,大多数来自外源性蛋白的肽可能被排除在参与CD4 + T细胞的阳性选择之外。