Institute of Development, Aging and Cancer, Tohoku University, Sendai, Isehara, Japan.
Immunology. 2011 Feb;132(2):157-64. doi: 10.1111/j.1365-2567.2010.03381.x. Epub 2010 Nov 23.
Over the past years, increasing numbers of distinct subsets have been discovered and identified for a T lymphocytes' entity. Differentiation and function of each T cell subset are controlled by a specific master transcription factor. Importantly, Runt-related transcription factors, particularly Runx1 and Runx3, interplay with these master regulators in various aspects of T cells' immunity. In this review article, we first explain roles of Th-Pok and Runx3 in differentiation of CD4 versus CD8 single positive cells, and later focus on cross-regulation of Th-Pok and Runx3 and their relationship with other factors such as TCR strength. Next, we provide evidences for the direct interplay of Runx1/3 with T-bet and GATA3 during Th1 versus Th2 commitment to activate or silence transcription of signature cytokine genes, IFNγ and IL4. Lastly, we explain feed-forward relationship between Runx1 and Foxp3 and discuss roles of Runx1 in regulatory T cells' suppressive activity. This review highlights an essential importance of Runx molecules in controlling various T cell subsets' differentiation and functions through molecular interplay with the master transcription factors in terms of protein-protein interaction as well as regulation of gene expression.
在过去的几年中,人们发现并鉴定了越来越多的 T 淋巴细胞实体的不同亚群。每个 T 细胞亚群的分化和功能都受特定的主转录因子控制。重要的是,Runt 相关转录因子,特别是 Runx1 和 Runx3,在 T 细胞免疫的各个方面与这些主调控因子相互作用。在这篇综述文章中,我们首先解释了 Th-Pok 和 Runx3 在 CD4 与 CD8 单阳性细胞分化中的作用,然后重点介绍了 Th-Pok 和 Runx3 的交叉调控及其与其他因素(如 TCR 强度)的关系。接下来,我们提供了证据表明 Runx1/3 与 T-bet 和 GATA3 在 Th1 与 Th2 分化过程中的直接相互作用,以激活或沉默特征细胞因子基因 IFNγ 和 IL4 的转录。最后,我们解释了 Runx1 与 Foxp3 之间的正反馈关系,并讨论了 Runx1 在调节性 T 细胞抑制活性中的作用。本综述强调了 Runx 分子通过与主转录因子的蛋白-蛋白相互作用以及基因表达调控,在控制各种 T 细胞亚群的分化和功能方面的重要性。