Tsinghua University Institute for Immunology and School of Medicine, Beijing 100084, China; Institute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University, Chongqing 400038, China.
Tsinghua University Institute for Immunology and School of Medicine, Beijing 100084, China.
Cell Rep. 2016 Feb 23;14(7):1735-1747. doi: 10.1016/j.celrep.2016.01.038. Epub 2016 Feb 11.
T follicular helper (Tfh) cell is a unique T cell subset specialized in promoting humoral immunity. B-cell lymphoma 6 protein (Bcl6) has been identified as an obligatory transcription factor in Tfh cells; however, the molecular mechanism underlying Bcl6 function remains largely unknown. Here, we defined Bcl6 target genes in Tfh cells by analyzing genome-wide Bcl6 occupancy together with transcriptome profiling. With consensus sequences being different from those in Th9, B cells, and macrophages, Bcl6 binding in Tfh cell was closely associated with a decrease in 5-hydroxymethylcytosine (5hmC). Importantly, Bcl6 promoted Tfh cell differentiation through antagonizing IL-7R (CD127)/signal transducer and activator of transcription (STAT) 5 axis; deletion of the Bcl6 gene in T cells resulted in enhanced IL-7R-STAT5 signaling and substantial expansion of CD127(hi) non-Tfh cells. Thus, our study systemically examines Bcl6-controlled regulatory networks and provides important insights into Bcl6's biological functions in Tfh cells.
滤泡辅助性 T 细胞(Tfh)是一类特化的 T 细胞亚群,专门用于促进体液免疫。B 细胞淋巴瘤 6 蛋白(Bcl6)已被鉴定为 Tfh 细胞中必需的转录因子;然而,Bcl6 功能的分子机制在很大程度上仍然未知。在这里,我们通过分析全基因组 Bcl6 结合位点与转录组谱,定义了 Tfh 细胞中的 Bcl6 靶基因。与 Th9、B 细胞和巨噬细胞中的结合序列不同,Tfh 细胞中的 Bcl6 结合与 5-羟甲基胞嘧啶(5hmC)的减少密切相关。重要的是,Bcl6 通过拮抗白细胞介素 7 受体(CD127)/信号转导和转录激活因子 5 轴促进 Tfh 细胞分化;T 细胞中 Bcl6 基因的缺失导致 IL-7R-STAT5 信号的增强和大量 CD127(高)非 Tfh 细胞的扩增。因此,我们系统地研究了 Bcl6 控制的调节网络,并为 Bcl6 在 Tfh 细胞中的生物学功能提供了重要的见解。