The Transcription Factors Thpok and LRF Are Necessary and Partly Redundant for T Helper Cell Differentiation

被引:35
作者
Carpenter, Andrea C. [1 ]
Grainger, John R. [2 ]
Xiong, Yumei [1 ]
Kanno, Yuka [3 ]
Chu, H. Hamlet [4 ]
Wang, Lie [1 ]
Naik, Shruti [2 ]
dos Santos, Liliane [2 ]
Wei, Lai [3 ]
Jenkins, Marc K. [4 ]
O'Shea, John J. [3 ]
Belkaid, Yasmine [2 ]
Bosselut, Remy [1 ]
机构
[1] NCI, Lab Immune Cell Biol, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] NIAID, Mucosal Immunol Sect, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[3] NIAMSD, Mol Immunol & Inflammat Branch, NIH, Bethesda, MD 20892 USA
[4] Univ Minnesota, Sch Med, Ctr Immunol, Dept Microbiol, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
ZINC-FINGER PROTEIN; LEISHMANIA-MAJOR INFECTION; LINEAGE FATE; GENE-EXPRESSION; CD4; EXPRESSION; COMMITMENT; RECEPTOR; SUPPRESSION; LYMPHOCYTES; ACTIVATION;
D O I
10.1016/j.immuni.2012.06.019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T helper (Th) cells are critical for defenses against infection and recognize peptides bound to class II major histocompatibility complex (MHC II) molecules. Although transcription factors have been identified that direct Th cells into specific effector fates, whether a "master" regulator controls the developmental program common to all Th cells remains unclear. Here, we showed that the two transcription factors Thpok and LRF share this function. Although disruption of both factors did not prevent the generation of MHC II-specific T cells, these cells failed to express Th cell genes or undergo Th cell differentiation in vivo. In contrast, T cells lacking Thpok, which only displayed LRF-dependent functions, contributed to multiple effector responses, both in vitro and in vivo, with the notable exception of Th2 cell responses that control extracellular parasites. These findings identify the Thpok-LRF pair as a core node of Th cell differentiation and function.
引用
收藏
页码:622 / 633
页数:12
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