Yu Qing, Erman Batu, Park Jung-Hyun, Feigenbaum Lionel, Singer Alfred
Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bldg. 10, Rm. 4B36, Bethesda, MD 20892, USA.
J Exp Med. 2004 Sep 20;200(6):797-803. doi: 10.1084/jem.20032183. Epub 2004 Sep 13.
Intrathymic T cell development depends on signals transduced by both T cell receptor and cytokine receptors. Early CD4(-)CD8(-) (double negative) thymocytes require interleukin (IL)-7 receptor (IL-7R) signals for survival and proliferation, but IL-7R signals are normally extinguished by the immature single positive (ISP) stage of thymocyte development. We now demonstrate that IL-7R signals inhibit expression of transcription factors TCF-1, LEF-1, and RORgammat that are required for the ISP to double positive (DP) transition in the thymus. In addition, we demonstrate that IL-7R signals also inhibit TCF-1 and LEF-1 expression in mature peripheral T cells. Thus, the present work has identified several important downstream target genes of IL-7R signaling in T cells and thymocytes that provide a molecular mechanism for the inhibitory influence of IL-7R signaling on DP thymocyte development. We conclude that IL-7R signals down-regulate transcription factors required for the ISP to DP transition and so must be terminated by the ISP stage of thymocyte development.
胸腺内T细胞的发育依赖于T细胞受体和细胞因子受体转导的信号。早期CD4(-)CD8(-)(双阴性)胸腺细胞需要白细胞介素(IL)-7受体(IL-7R)信号来维持生存和增殖,但IL-7R信号通常在胸腺细胞发育的未成熟单阳性(ISP)阶段被消除。我们现在证明,IL-7R信号抑制转录因子TCF-1、LEF-1和RORγt的表达,这些转录因子是胸腺中ISP向双阳性(DP)转变所必需的。此外,我们证明IL-7R信号也抑制成熟外周T细胞中TCF-1和LEF-1的表达。因此,本研究确定了T细胞和胸腺细胞中IL-7R信号的几个重要下游靶基因,这些基因为IL-7R信号对DP胸腺细胞发育的抑制作用提供了分子机制。我们得出结论,IL-7R信号下调了ISP向DP转变所需的转录因子,因此必须在胸腺细胞发育的ISP阶段被终止。