Grueter Baerbel, Petter Michaela, Egawa Takeshi, Laule-Kilian Kirsten, Aldrian Christine J, Wuerch Andreas, Ludwig Yvonne, Fukuyama Hidehiro, Wardemann Hedda, Waldschuetz Ralph, Möröy Tarik, Taniuchi Ichiro, Steimle Viktor, Littman Dan R, Ehlers Marc
Institute of Molecular Biology (Cancer Research), University of Essen, Medical School, Essen, Germany.
J Immunol. 2005 Aug 1;175(3):1694-705. doi: 10.4049/jimmunol.175.3.1694.
During thymic T cell development, immature CD4+CD8+ double-positive (DP) thymocytes develop either into CD4+CD8- Th cells or CD4-CD8+ CTLs. Differentially expressed primary factors inducing the fate of these cell types are still poorly described. The transcription factor Runx3/AML-2 Runx, runt [corrected] dominant factor; AML, acute myeloid leukemia is expressed specifically during the development of CD8 single-positive (SP) thymocytes, where it silences CD4 expression. Deletion of murine Runx3 results in a reduction of CD8 SP T cells and concomitant accumulation of CD4+CD8+ T cells, which cannot down-regulate CD4 expression in the thymus and periphery. In this study we have investigated the role of Runx3 during thymocyte development and CD4 silencing and have identified integrin alpha(E)/CD103 on CD8 SP T cells as a new potential target gene of Runx3. We demonstrate that Runx3 is necessary not only to repress CD4, but also to induce CD103 expression during development of CD8 SP T cells. In addition, transgenic overexpression of Runx3 reduced CD4 expression during development of DP thymocytes, leading to a reduced number of CD4 SP thymocytes and an increased number of CD8 SP thymocytes. This reversal is not caused by redirection of specific MHC class II-restricted cells to the CD8 lineage. Overexpression of Runx3 also up-regulated CD103 expression on a subpopulation of CD4 SP T cells with characteristics of regulatory T cells. Thus, Runx3 is a main regulator of CD4 silencing and CD103 induction and thus contributes to the phenotype of CD8 SP T cells during thymocyte development.
在胸腺T细胞发育过程中,未成熟的CD4⁺CD8⁺双阳性(DP)胸腺细胞会发育为CD4⁺CD8⁻辅助性T细胞或CD4⁻CD8⁺细胞毒性T淋巴细胞(CTL)。诱导这些细胞类型命运的差异表达主要因子仍未得到充分描述。转录因子Runx3/AML-2(Runx,矮小相关[校正]显性因子;AML,急性髓系白血病)在CD8单阳性(SP)胸腺细胞发育过程中特异性表达,在该过程中它会使CD4表达沉默。小鼠Runx3缺失会导致CD8 SP T细胞数量减少以及CD4⁺CD8⁺ T细胞的相应积累,这些细胞在胸腺和外周不能下调CD4表达。在本研究中,我们研究了Runx3在胸腺细胞发育和CD4沉默过程中的作用,并确定CD8 SP T细胞上的整合素α(E)/CD103是Runx3的一个新的潜在靶基因。我们证明Runx3不仅对于抑制CD4是必需的,而且在CD8 SP T细胞发育过程中诱导CD103表达也是必需的。此外,Runx3的转基因过表达在DP胸腺细胞发育过程中降低了CD4表达,导致CD4 SP胸腺细胞数量减少以及CD8 SP胸腺细胞数量增加。这种逆转不是由特定的MHC II类限制性细胞重定向到CD8谱系引起的。Runx3的过表达还上调了具有调节性T细胞特征的CD4 SP T细胞亚群上的CD103表达。因此,Runx3是CD4沉默和CD103诱导的主要调节因子,从而在胸腺细胞发育过程中促成了CD8 SP T细胞的表型。