Park J H, Mitnacht R, Torres-Nagel N, Hünig T
Institute of Virology and Immunobiology, University of Würzburg, FRG.
J Exp Med. 1993 Feb 1;177(2):541-6. doi: 10.1084/jem.177.2.541.
The role of interleukin (IL)2 in intrathymic T cell development is highly controversial, and nothing is known about IL-2R expression on thymocytes of the T cell receptor (TCR) alpha/beta lineage undergoing TCR-driven differentiation events. We analyze here IL-2R alpha and beta mRNA expression in an in vitro system where newly generated rat CD4,8 double positive (DP) thymocytes respond to TCR ligation plus IL-2 (but not to either stimulus alone) with rapid differentiation to functional CD8 single positive T cells (Hünig, T., and R. Mitnacht. 1991. J. Exp. Med. 173:561). TCR ligation induced expression of IL-2R beta (but not alpha) chain mRNA in DP thymocytes. Addition of IL-2 then lead to functional maturation and expression of the IL-2R alpha chain. To investigate if the CD8 T cells generated via this IL-2R beta-driven pathway in vitro correspond to the bulk of CD8 T cells seeding peripheral lymphoid organs in vivo, we compared their phenotype to that of lymph node CD8 T cells. Surprisingly, analysis of CD8 cell surface expression using a novel anti-CD8 monoclonal antibody specific for the alpha/beta heterodimeric isoform, and of CD8 alpha and beta chain mRNA revealed that T cells generated by TCR ligation plus IL-2 resemble thymus-independent rather than thymus-derived CD8 cells in that they express CD8 alpha without beta chains. These findings demonstrate that TCR crosslinking induces functional IL-2R on immature DP rat thymocytes. In addition, they show that at least in vitro, CD8 alpha/alpha T cells are generated from TCR-stimulated DP thymocytes (which express the CD8 alpha/beta in the heterodimeric isoform) along an IL-2-driven pathway of T cell differentiation.
白细胞介素(IL)-2在胸腺内T细胞发育中的作用极具争议,对于经历T细胞受体(TCR)α/β谱系TCR驱动分化事件的胸腺细胞上IL-2受体(IL-2R)的表达情况,我们一无所知。在此,我们分析了体外系统中新生大鼠CD4、8双阳性(DP)胸腺细胞的IL-2Rα和β mRNA表达情况,在该系统中,新生成的大鼠CD4、8双阳性胸腺细胞对TCR连接加上IL-2(而非单独的任何一种刺激)作出反应,迅速分化为功能性CD8单阳性T细胞(许尼希,T.,和R. 米特纳赫特。1991年。《实验医学杂志》173:561)。TCR连接诱导DP胸腺细胞中IL-2Rβ(而非α)链mRNA的表达。添加IL-2随后导致功能成熟和IL-2Rα链的表达。为了研究通过体外这种由IL-2Rβ驱动的途径产生的CD8 T细胞是否与体内播种到外周淋巴器官的大部分CD8 T细胞相对应,我们将它们的表型与淋巴结CD8 T细胞的表型进行了比较。令人惊讶的是,使用一种针对α/β异二聚体异构体的新型抗CD8单克隆抗体对CD8细胞表面表达进行分析,以及对CD8α和β链mRNA进行分析发现,由TCR连接加IL-2产生的T细胞类似于非胸腺依赖性而非胸腺来源的CD8细胞,因为它们表达没有β链的CD8α。这些发现表明,TCR交联在未成熟的DP大鼠胸腺细胞上诱导功能性IL-2R。此外,它们表明至少在体外,CD8α/α T细胞是由TCR刺激的DP胸腺细胞(其以异二聚体异构体形式表达CD8α/β)沿着IL-2驱动的T细胞分化途径产生的。