BCL6公司
生发中心
效应器
生物
细胞生物学
B细胞
细胞分化
转录因子
T细胞
免疫学
抗体
细胞毒性T细胞
免疫系统
体外
遗传学
基因
作者
Robert J. Johnston,Amanda C. Poholek,Daniel DiToro,Isharat Yusuf,Danelle S. Eto,Burton E. Barnett,Alexander L. Dent,Joe Craft,Shane Crotty
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2009-07-17
卷期号:325 (5943): 1006-1010
被引量:1551
标识
DOI:10.1126/science.1175870
摘要
Effective B cell-mediated immunity and antibody responses often require help from CD4+ T cells. It is thought that a distinct CD4+ effector T cell subset, called T follicular helper cells (T(FH)), provides this help; however, the molecular requirements for T(FH) differentiation are unknown. We found that expression of the transcription factor Bcl6 in CD4+ T cells is both necessary and sufficient for in vivo T(FH) differentiation and T cell help to B cells in mice. In contrast, the transcription factor Blimp-1, an antagonist of Bcl6, inhibits T(FH) differentiation and help, thereby preventing B cell germinal center and antibody responses. These findings demonstrate that T(FH) cells are required for proper B cell responses in vivo and that Bcl6 and Blimp-1 play central but opposing roles in T(FH) differentiation.
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