Institute of Immunology, Third Military Medical University, Chongqing, China.
1] Ministry of Education Key Laboratory for Avian Preventive Medicine, Yangzhou University, Yangzhou, China. [2] Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, China.
Nat Immunol. 2015 Sep;16(9):991-9. doi: 10.1038/ni.3229. Epub 2015 Jul 27.
Induction of the transcriptional repressor Bcl-6 in CD4(+) T cells is critical for the differentiation of follicular helper T cells (T(FH) cells), which are essential for B cell-mediated immunity. In contrast, the transcription factor Blimp1 (encoded by Prdm1) inhibits T(FH) differentiation by antagonizing Bcl-6. Here we found that the transcription factor TCF-1 was essential for both the initiation of T(FH) differentiation and the effector function of differentiated T(FH) cells during acute viral infection. Mechanistically, TCF-1 bound directly to the Bcl6 promoter and Prdm1 5' regulatory regions, which promoted Bcl-6 expression but repressed Blimp1 expression. TCF-1-null T(FH) cells upregulated genes associated with non-T(FH) cell lineages. Thus, TCF-1 functions as an important hub upstream of the Bcl-6-Blimp1 axis to initiate and secure the differentiation of T(FH) cells during acute viral infection.
诱导 CD4(+) T 细胞中的转录抑制因子 Bcl-6 对于滤泡辅助 T 细胞(T(FH) 细胞)的分化至关重要,T(FH) 细胞对于 B 细胞介导的免疫是必需的。相比之下,转录因子 Blimp1(由 Prdm1 编码)通过拮抗 Bcl-6 抑制 T(FH)分化。在这里,我们发现转录因子 TCF-1 在急性病毒感染期间,对于 T(FH)分化的起始和分化的 T(FH)细胞的效应功能都是必需的。在机制上,TCF-1 直接结合到 Bcl6 启动子和 Prdm1 5'调控区,这促进了 Bcl-6 的表达,但抑制了 Blimp1 的表达。TCF-1 缺陷型 T(FH)细胞上调与非 T(FH)细胞谱系相关的基因。因此,TCF-1 作为 Bcl-6-Blimp1 轴的一个重要枢纽,在急性病毒感染期间启动并确保 T(FH)细胞的分化。