Center for Agricultural Biomaterials, Seoul National University, Seoul 151-921, Korea.
Immune Netw. 2011 Dec;11(6):336-41. doi: 10.4110/in.2011.11.6.336. Epub 2011 Dec 31.
T cell receptor (TCR) signaling plays a critical role in T cell development, survival and differentiation. In the thymus, quantitative and/or qualitative differences in TCR signaling determine the fate of developing thymocytes and lead to positive and negative selection. Recently, it has been suggested that self-reactive T cells, escape from negative selection, should be suppressed in the periphery by regulatory T cells (Tregs) expressing Foxp3 transcription factor. Foxp3 is a master factor that is critical for not only development and survival but also suppressive activity of Treg. However, signals that determine Treg fate are not completely understood. The availability of mutant mice which harbor mutations in TCR signaling mediators will certainly allow to delineate signaling events that control intrathymic (natural) Treg (nTreg) development. Thus, we summarize the recent progress on the role of TCR signaling cascade components in nTreg development from the studies with murine model.
T 细胞受体(TCR)信号在 T 细胞的发育、存活和分化中起着关键作用。在胸腺中,TCR 信号的数量和/或质量差异决定了发育中的胸腺细胞的命运,并导致阳性和阴性选择。最近,有人提出,逃避负选择的自身反应性 T 细胞应该被表达 Foxp3 转录因子的调节性 T 细胞(Treg)在周围组织中抑制。Foxp3 是一个关键的主调控因子,不仅对 Treg 的发育和存活至关重要,而且对其抑制活性也至关重要。然而,决定 Treg 命运的信号还不完全清楚。TCR 信号转导介质突变小鼠的出现,必将有助于描绘控制胸腺内(天然)调节性 T 细胞(nTreg)发育的信号事件。因此,我们从鼠模型的研究中总结了 TCR 信号级联成分在 nTreg 发育中的作用的最新进展。