Chronic Immune Reactions, German Rheumatism Research Center, 10117 Berlin, Germany; and.
Therapeutic Gene Regulation, German Rheumatism Research Center, 10117 Berlin, Germany.
J Immunol. 2019 Apr 15;202(8):2229-2239. doi: 10.4049/jimmunol.1801400. Epub 2019 Mar 4.
T follicular helper (Tfh) cells are a specialized T cell subset that regulates the long-lived production of highly specific Abs by B cells during the germinal center (GC) reaction. However, the transcriptional network sustaining the Tfh cell phenotype and function is still incompletely understood. In this study, we identify the transcription factor Bach2 as a central negative regulator of Tfh cells. Ectopic overexpression of Bach2 in murine Tfh cells resulted in a rapid loss of their phenotype and subsequent breakdown of the GC response. Low Bach2 expression levels are required to maintain high expression of the signature cytokine IL-21, the coinhibitory receptor TIGIT and the transcriptional repressor Bcl-6. In stark contrast to the regulatory network in GC B cells, Bach2 in Tfh cells is not coexpressed with Bcl-6 at high levels to inhibit the antagonizing factor Blimp-1, but suppresses Bcl-6 by direct binding to the promoter. These data reveal that by replacing an activating complex of Batf and Irf-4 at the Bcl-6 promoter, Bach2 regulates the transcriptional network of Tfh cells in a different way, as in GC B cells.
滤泡辅助 T 细胞(Tfh)是一种特殊的 T 细胞亚群,在生发中心(GC)反应期间调节 B 细胞产生高度特异性抗体的长期产生。然而,维持 Tfh 细胞表型和功能的转录网络仍不完全清楚。在这项研究中,我们确定转录因子 Bach2 是 Tfh 细胞的中央负调节因子。Bach2 在小鼠 Tfh 细胞中的异位过表达导致其表型迅速丧失,随后 GC 反应崩溃。低 Bach2 表达水平是维持特征细胞因子 IL-21、共抑制受体 TIGIT 和转录抑制因子 Bcl-6 高表达所必需的。与 GC B 细胞中的调节网络形成鲜明对比的是,Tfh 细胞中的 Bach2 不会与 Bcl-6 高水平共表达以抑制拮抗因子 Blimp-1,而是通过直接结合启动子来抑制 Bcl-6。这些数据表明,Bach2 通过取代 Bcl-6 启动子上的 Batf 和 Irf-4 激活复合物,以不同于 GC B 细胞中的方式调节 Tfh 细胞的转录网络。