Interplay of transcription factors in T-cell differentiation and function: the role of Runx

被引:91
作者
Wong, Won Fen [1 ]
Kohu, Kazuyoshi [1 ]
Chiba, Tomoki [2 ]
Sato, Takehito [2 ]
Satake, Masanobu [1 ]
机构
[1] Tohoku Univ, Inst Dev Aging & Canc, Grad Sch Life Sci,Ctr Regulatory Epigenome & Dis, Dept Mol Immunol,Grad Sch Med,Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tokai Univ, Sch Med, Dept Immunol, Isehara, Kanagawa 25911, Japan
基金
日本学术振兴会;
关键词
cell differentiation; gene expression; gene targeting; T lymphocytes; transcription factor; LINEAGE DIFFERENTIATION; CD4; EXPRESSION; THPOK; FOXP3; REPRESSION; AML1; OVEREXPRESSION; COMMITMENT; THYMOCYTES; PROTEINS;
D O I
10.1111/j.1365-2567.2010.03381.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
P>Over the past years, increasing numbers of distinct subsets have been discovered and identified for a T lymphocytes' entity. Differentiation and function of each T cell subset are controlled by a specific master transcription factor. Importantly, Runt-related transcription factors, particularly Runx1 and Runx3, interplay with these master regulators in various aspects of T cells' immunity. In this review article, we first explain roles of Th-Pok and Runx3 in differentiation of CD4 versus CD8 single positive cells, and later focus on cross-regulation of Th-Pok and Runx3 and their relationship with other factors such as TCR strength. Next, we provide evidences for the direct interplay of Runx1/3 with T-bet and GATA3 during Th1 versus Th2 commitment to activate or silence transcription of signature cytokine genes, IFN gamma and IL4. Lastly, we explain feed-forward relationship between Runx1 and Foxp3 and discuss roles of Runx1 in regulatory T cells' suppressive activity. This review highlights an essential importance of Runx molecules in controlling various T cell subsets' differentiation and functions through molecular interplay with the master transcription factors in terms of protein-protein interaction as well as regulation of gene expression.
引用
收藏
页码:157 / 164
页数:8
相关论文
共 63 条
[1]   Reduction of runx1 transcription factor activity up-regulates Fas and Bim expression and enhances the apoptotic sensitivity of double positive thymocytes [J].
Abe, N ;
Kohu, K ;
Ohmori, H ;
Hayashi, K ;
Watanabe, T ;
Hozumi, K ;
Sato, T ;
Habu, S ;
Satake, M .
JOURNAL OF IMMUNOLOGY, 2005, 175 (07) :4475-4482
[2]   The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3 [J].
Bennett, CL ;
Christie, J ;
Ramsdell, F ;
Brunkow, ME ;
Ferguson, PJ ;
Whitesell, L ;
Kelly, TE ;
Saulsbury, FT ;
Chance, PF ;
Ochs, HD .
NATURE GENETICS, 2001, 27 (01) :20-21
[3]   Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse [J].
Brunkow, ME ;
Jeffery, EW ;
Hjerrild, KA ;
Paeper, B ;
Clark, LB ;
Yasayko, SA ;
Wilkinson, JE ;
Galas, D ;
Ziegler, SF ;
Ramsdell, F .
NATURE GENETICS, 2001, 27 (01) :68-73
[4]   Runx proteins regulate Foxp3 expression [J].
Bruno, Ludovica ;
Mazzarella, Luca ;
Hoogenkamp, Maarten ;
Hertweck, Arnulf ;
Cobb, Bradley S. ;
Sauer, Stephan ;
Hadjur, Suzana ;
Leleu, Marion ;
Naoe, Yoshinori ;
Telfer, Janice C. ;
Bonifer, Constanze ;
Taniuchi, Ichiro ;
Fisher, Amanda G. ;
Merkenschlager, Matthias .
JOURNAL OF EXPERIMENTAL MEDICINE, 2009, 206 (11) :2329-2337
[5]   The Runx3 distal transcript encodes an additional transcriptional activation domain [J].
Chung, David D. ;
Honda, Kazuho ;
Cafuir, Lorraine ;
McDuffie, Marcia ;
Wotton, David .
FEBS JOURNAL, 2007, 274 (13) :3429-3439
[6]   RUNX proteins in transcription factor networks that regulate T-cell lineage choice [J].
Collins, Amelie ;
Littman, Dan R. ;
Taniuchi, Ichiro .
NATURE REVIEWS IMMUNOLOGY, 2009, 9 (02) :106-115
[7]   HD mice:: A novel mouse mutant with a specific defect in the generation of CD4+ T cells [J].
Dave, VP ;
Allman, D ;
Keefe, R ;
Hardy, RR ;
Kappes, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (14) :8187-8192
[8]   Transcription factors T-bet and Runx3 cooperate to activate lfng and silence ll4 in T helper type 1 cells [J].
Djuretic, Ivana M. ;
Levanon, Ditsa ;
Negreanu, Varda ;
Groner, Yoram ;
Rao, Anjana ;
Ansel, K. Mark .
NATURE IMMUNOLOGY, 2007, 8 (02) :145-153
[9]   Genetic evidence supporting selection of the Vα14i NKT cell lineage from double-positive thymocyte precursors [J].
Egawa, T ;
Eberl, G ;
Taniuchi, I ;
Benlagha, K ;
Geissmann, F ;
Hennighausen, L ;
Bendelac, A ;
Littman, DR .
IMMUNITY, 2005, 22 (06) :705-716
[10]   ThPOK acts late in specification of the helper T cell lineage and suppresses Runx-mediated commitment to the cytotoxic T cell lineage [J].
Egawa, Takeshi ;
Littman, Dan R. .
NATURE IMMUNOLOGY, 2008, 9 (10) :1131-1139