生发中心
CD40
细胞生物学
转录因子
生物
下调和上调
细胞因子
B细胞
亲和力成熟
抗体
分子生物学
化学
免疫学
体外
基因
细胞毒性T细胞
遗传学
作者
Jason S. Weinstein,Edward I. Herman,Begoña Lainez,Paula Licona-Limón,Enric Esplugues,Richard A. Flavell,Joe Craft
出处
期刊:Nature Immunology
[Nature Portfolio]
日期:2016-08-29
卷期号:17 (10): 1197-1205
被引量:400
摘要
Germinal center (GC) B cells undergo affinity selection, which depends on interactions with CD4(+) follicular helper T cells (TFH cells). We found that TFH cells progressed through transcriptionally and functionally distinct stages and provided differential signals for GC regulation. They initially localized proximally to mutating B cells, secreted interleukin 21 (IL-21), induced expression of the transcription factor Bcl-6 and selected high-affinity B cell clones. As the GC response evolved, TFH cells extinguished IL-21 production and switched to IL-4 production, showed robust expression of the co-stimulatory molecule CD40L, and promoted the development of antibody-secreting B cells via upregulation of the transcription factor Blimp-1. Thus, TFH cells in the B cell follicle progressively differentiate through stages of localization, cytokine production and surface ligand expression to 'fine tune' the GC reaction.
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