Molecular Mechanisms Regulating T Helper 1 versus T Follicular Helper Cell Differentiation in Humans

被引:41
|
作者
Schmitt, Nathalie [1 ,2 ]
Liu, Yang [1 ]
Bentebibel, Salah-Eddine [1 ]
Ueno, Hideki [1 ,3 ]
机构
[1] Baylor Res Inst, Baylor Inst Immunol Res, Dallas, TX 75204 USA
[2] Univ Bordeaux, CNRS UMR 5164, F-33076 Bordeaux, France
[3] Icahn Sch Med Mt Sinai, Global Hlth & Emerging Pathogens Inst, Dept Microbiol, New York, NY 10029 USA
来源
CELL REPORTS | 2016年 / 16卷 / 04期
关键词
TRANSCRIPTION FACTOR IRF4; CENTER B-CELL; BCL6; EXPRESSION; BET; MIGRATION; NAIVE; PROMOTE; LINEAGE; ROLES;
D O I
10.1016/j.celrep.2016.06.063
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
IL-12 is important for the differentiation of T follicular helper (Tfh) cells, as well as Th1 cells in humans. Still, how IL-12 signals regulate Tfh versus Th1 cell differentiation remains poorly characterized. Here we aimed to determine the molecular mechanisms that regulate the differentiation and the function of IL-12-stimulated human naive CD4(+) T cells. We found that T-bet promoted the expression of CXCR5 in human CD4(+) T cells. We provide evidence that T-bet does not strongly inhibit the Tfh cell differentiation program per se but diminishes the functions to provide help to B cells. This study also suggests that IRF4 plays an important role in driving the early differentiation of IL-12-stimulated CD4(+) T cells toward Tfh and away from Th1 by inhibiting the expression of Eomesodermin. Thus, the fate of IL-12-stimulated CD4+ T cells is determined through interplay of multiple transcription factors at early stages.
引用
收藏
页码:1082 / 1095
页数:14
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