TCF-1: a maverick in T cell development and function

被引:44
作者
Gounari, Fotini [1 ,2 ]
Khazaie, Khashayarsha [2 ]
机构
[1] Univ Chicago, Dept Med, Knapp Res Ctr, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USA
[2] Mayo Clin, Dept Immunol, Scottsdale, AZ 85259 USA
基金
美国国家卫生研究院;
关键词
EDGE BETA-CATENIN; TRANSCRIPTION FACTORS; HMG DOMAIN; FACTOR-I; DIFFERENTIATION; EFFECTOR; LINEAGE; LEF-1; SPECIFICATION; CHROMATIN;
D O I
10.1038/s41590-022-01194-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The T cell-specific DNA-binding protein TCF-1 is a central regulator of T cell development and function along multiple stages and lineages. Because it interacts with beta-catenin, TCF-1 has been classically viewed as a downstream effector of canonical Wnt signaling, although there is strong evidence for beta-catenin-independent TCF-1 functions. TCF-1 co-binds accessible regulatory regions containing or lacking its conserved motif and cooperates with other nuclear factors to establish context-dependent epigenetic and transcription programs that are essential for T cell development and for regulating immune responses to infection, autoimmunity and cancer. Although it has mostly been associated with positive regulation of chromatin accessibility and gene expression, TCF-1 has the potential to reduce chromatin accessibility and thereby suppress gene expression. In addition, the binding of TCF-1 bends the DNA and affects the chromatin conformation genome wide. This Review discusses the current understanding of the multiple roles of TCF-1 in T cell development and function and their mechanistic underpinnings. The transcription factor TCF-1 has multiple roles during T cell development and in mature T cells. Gounari and Khazaie review the potential mechanisms by which TCF-1 regulates gene expression.
引用
收藏
页码:671 / 678
页数:8
相关论文
共 113 条
[41]   Metabolic heterogeneity underlies reciprocal fates of TH17 cell sternness and plasticity [J].
Karmaus, Peer W. F. ;
Chen, Xiang ;
Lim, Seon Ah ;
Herrada, Andres A. ;
Nguyen, Thanh-Long M. ;
Xu, Beisi ;
Dhungana, Yogesh ;
Rankin, Sherri ;
Chen, Wenan ;
Rosencrance, Celeste ;
Yang, Kai ;
Fan, Yiping ;
Cheng, Yong ;
Easton, John ;
Neale, Geoffrey ;
Vogel, Peter ;
Chi, Hongbo .
NATURE, 2019, 565 (7737) :101-+
[42]   Multi-transcription factor reporter mice delineate early precursors to the ILC and LTi lineages [J].
Kasal, Darshan N. ;
Bendelac, Albert .
JOURNAL OF EXPERIMENTAL MEDICINE, 2021, 218 (02)
[43]   β-Catenin Promotes Colitis and Colon Cancer Through Imprinting of Proinflammatory Properties in T Cells [J].
Keerthivasan, Shilpa ;
Aghajani, Katayoun ;
Dose, Marei ;
Molinero, Luciana ;
Khan, Mohammad W. ;
Venkateswaran, Vysak ;
Weber, Christopher ;
Emmanuel, Akinola Olumide ;
Sun, Tianjao ;
Bentrem, David J. ;
Mulcahy, Mary ;
Keshavarzian, Ali ;
Ramos, Elena M. ;
Blatner, Nichole ;
Khazaie, Khashayarsha ;
Gounari, Fotini .
SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (225)
[44]   TOX transcriptionally and epigenetically programs CD8+ T cell exhaustion [J].
Khan, Omar ;
Giles, Josephine R. ;
McDonald, Sierra ;
Manne, Sasikanth ;
Ngiow, Shin Foong ;
Patel, Kunal P. ;
Werner, Michael T. ;
Huang, Alexander C. ;
Alexander, Katherine A. ;
Wu, Jennifer E. ;
Attanasio, John ;
Yan, Patrick ;
George, Sangeeth M. ;
Bengsch, Bertram ;
Staupe, Ryan P. ;
Donahue, Greg ;
Xu, Wei ;
Amaravadi, Ravi K. ;
Xu, Xiaowei ;
Karakousis, Giorgos C. ;
Mitchell, Tara C. ;
Schuchter, Lynn M. ;
Kaye, Jonathan ;
Berger, Shelley L. ;
Wherry, E. John .
NATURE, 2019, 571 (7764) :211-+
[45]   Simultaneous loss of β- and γ-catenin does not perturb hematopoiesis or lymphopoiesis [J].
Koch, Ute ;
Wilson, Anne ;
Cobas, Monica ;
Kemler, Rolf ;
MacDonald, H. Robson ;
Radtke, Freddy .
BLOOD, 2008, 111 (01) :160-164
[46]   Asynchronous combinatorial action of four regulatory factors activates Bcl11b for T cell commitment [J].
Kueh, Hao Yuan ;
Yui, Mary A. ;
Ng, Kenneth K. H. ;
Pease, Shirley S. ;
Zhang, Jingli A. ;
Damle, Sagar S. ;
Freedman, George ;
Siu, Sharmayne ;
Bernstein, Irwin D. ;
Elowitz, Michael B. ;
Rothenberg, Ellen V. .
NATURE IMMUNOLOGY, 2016, 17 (08) :956-+
[47]   Checkpoint Blockade Immunotherapy Induces Dynamic Changes in PD-1-CD8+ Tumor-Infiltrating T Cells [J].
Kurtulus, Sema ;
Madi, Asaf ;
Escobar, Giulia ;
Klapholz, Max ;
Nyman, Jackson ;
Christian, Elena ;
Pawlak, Mathias ;
Dionne, Danielle ;
Xia, Junrong ;
Rozenblatt-Rosen, Orit ;
Kuchroo, Vijay K. ;
Regev, Aviv ;
Anderson, Ana C. .
IMMUNITY, 2019, 50 (01) :181-+
[48]   Wnt Signaling in Normal and Malignant Hematopoiesis [J].
Lento, William ;
Congdon, Kendra ;
Voermans, Carlijn ;
Kritzik, Marcie ;
Reya, Tannishtha .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2013, 5 (02)
[49]   TFH cells depend on Tcf1-intrinsic HDAC activity to suppress CTLA4 and guard B-cell help function [J].
Li, Fengyin ;
Zhao, Xin ;
Zhang, Yali ;
Shao, Peng ;
Ma, Xiaoke ;
Paradee, William J. ;
Liu, Chengyu ;
Wang, Jianmin ;
Xue, Hai-Hui .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2021, 118 (02)
[50]   TOX as a potential target for immunotherapy in lymphocytic malignancies [J].
Liang, Chaofeng ;
Huang, Shuxin ;
Zhao, Yujie ;
Chen, Shaohua ;
Li, Yangqiu .
BIOMARKER RESEARCH, 2021, 9 (01)