Bendelac A
Laboratory of Cellular and Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
Semin Immunol. 1992 Jun;4(3):187-93.
The generation of mouse CD4+8- thymocytes appears to involve an activation process. CD69, an early activation marker, is first expressed on 3% of TCRlo/med double-positive thymocytes and peaks (70-90%) at the HSAhi TCRmed CD4+8lo and the HSAhi TCRhi CD4+8- stages, before being downmodulated. CD44, a marker of a later stage of activation is selectively expressed at the HSAlo CD4+8- stage. Functional changes associated with the late activated state, such as the transient acquisition of the potential to secrete IL-4 upon stimulation, are also induced at the HSAlo CD4+8- stage and are still evident after export to the periphery. During thymic selection, interactions of different affinities between TCR/CD4 and self ligand/MHC class II, are likely to induce different degrees of activation. This may impart different functional capabilities--such as the potential to secrete IL-4--to a subset of emerging CD4+ T lymphocytes that express TCRs with intermediate affinities for self. Such a pathway may be involved in the maintenance of tolerance and the prevention of some deleterious autoimmune reactions.
小鼠CD4+8-胸腺细胞的产生似乎涉及一个激活过程。早期激活标志物CD69首先在3%的TCRlo/med双阳性胸腺细胞上表达,并在HSAhi TCRmed CD4+8lo和HSAhi TCRhi CD4+8-阶段达到峰值(70-90%),然后下调。激活后期标志物CD44在HSAlo CD4+8-阶段选择性表达。与后期激活状态相关的功能变化,如刺激后短暂获得分泌IL-4的潜能,也在HSAlo CD4+8-阶段诱导产生,并且在输出到外周后仍然明显。在胸腺选择过程中,TCR/CD4与自身配体/MHC II类之间不同亲和力的相互作用可能诱导不同程度的激活。这可能赋予一部分新出现的对自身具有中等亲和力的TCR的CD4+ T淋巴细胞不同的功能能力,如分泌IL-4的潜能。这样的途径可能参与耐受性的维持和一些有害自身免疫反应的预防。