BCL6公司
生发中心
状态4
生物
T细胞
免疫学
T辅助细胞
癌症研究
B细胞
抗体
细胞生物学
信号转导
免疫系统
车站3
斯达
作者
Jason S. Weinstein,Brian J. Laidlaw,Yisi Lu,Jessica K. Wang,Vincent Schulz,Ningcheng Li,Edward I. Herman,Susan M. Kaech,Patrick G. Gallagher,Joe Craft
摘要
Follicular helper T (Tfh) cells promote germinal center (GC) B cell survival and proliferation and guide their differentiation and immunoglobulin isotype switching by delivering contact-dependent and soluble factors, including IL-21, IL-4, IL-9, and IFN-γ. IL-21 and IFN-γ are coexpressed by Tfh cells during viral infections, but transcriptional regulation of these cytokines is not completely understood. In this study, we show that the T helper type 1 cell (Th1 cell) transcriptional regulators T-bet and STAT4 are coexpressed with Bcl6 in Tfh cells after acute viral infection, with a temporal decline in T-bet in the waning response. T-bet is important for Tfh cell production of IFN-γ, but not IL-21, and for a robust GC reaction. STAT4, phosphorylated in Tfh cells upon infection, is required for expression of T-bet and Bcl6 and for IFN-γ and IL-21. These data indicate that T-bet is expressed with Bcl6 in Tfh cells and is required alongside STAT4 to coordinate Tfh cell IL-21 and IFN-γ production and for promotion of the GC response after acute viral challenge.
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