Bcl-6 is the nexus transcription factor of T follicular helper cells via repressor-of-repressor circuits

被引:105
作者
Choi, Jinyong [1 ]
Diao, Huitian [2 ]
Faliti, Caterina E. [1 ]
Truong, Jacquelyn [1 ]
Rossi, Meghan [1 ]
Belanger, Simon [1 ]
Yu, Bingfei [3 ]
Goldrath, Ananda W. [3 ]
Pipkin, Matthew E. [2 ]
Crotty, Shane [1 ,4 ]
机构
[1] La Jolla Inst Immunol, Ctr Infect Dis & Vaccine Res, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Immunol & Microbiol, Jupiter, FL USA
[3] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Med, Div Infect Dis & Global Publ Hlth, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
NEGATIVE REGULATOR; B-CELLS; DIFFERENTIATION; BLIMP-1; GENE; EXPRESSION; DOMAIN; COREPRESSOR; INHIBITION; LANDSCAPES;
D O I
10.1038/s41590-020-0706-5
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 follicular helper (T-FH) cells are a distinct type of CD4(+)T cells that are essential for most antibody and B lymphocyte responses. T(FH)cell regulation and dysregulation is involved in a range of diseases. Bcl-6 is the lineage-defining transcription factor of T(FH)cells and its activity is essential for T(FH)cell differentiation and function. However, how Bcl-6 controls T(FH)biology has largely remained unclear, at least in part due to the intrinsic challenges of connecting repressors to gene upregulation in complex cell types with multiple possible differentiation fates. Multiple competing models were tested here by a series of experimental approaches to determine that Bcl-6 exhibits negative autoregulation and controls pleiotropic attributes of T(FH)differentiation and function, including migration, costimulation, inhibitory receptors and cytokines, via multiple repressor-of-repressor gene circuits. Bcl-6 is the signature transcription factor for T(FH)cells. Crotty and colleagues provide a comprehensive transcriptional map depicting the regulatory circuitry controlled by Bcl-6 in determining T(FH)cell fate and function.
引用
收藏
页码:777 / +
页数:26
相关论文
共 63 条
[11]   Bach2 Negatively Regulates T Follicular Helper Cell Differentiation and Is Critical for CD4+ T Cell Memory [J].
Geng, Jianlin ;
Wei, Hairong ;
Shi, Bi ;
Wang, Yin-Hu ;
Greer, Braxton D. ;
Pittman, Melanie ;
Smith, Emily ;
Thomas, Paul G. ;
Kutsch, Olaf ;
Hu, Hui .
JOURNAL OF IMMUNOLOGY, 2019, 202 (10) :2991-2998
[12]   BCL6 orchestrates Tfh cell differentiation via multiple distinct mechanisms [J].
Hatzi, Katerina ;
Nance, J. Philip ;
Kroenke, Mark A. ;
Bothwell, Marcella ;
Haddad, Elias K. ;
Melnick, Ari ;
Crotty, Shane .
JOURNAL OF EXPERIMENTAL MEDICINE, 2015, 212 (04) :539-553
[13]   A Hybrid Mechanism of Action for BCL6 in B Cells Defined by Formation of Functionally Distinct Complexes at Enhancers and Promoters [J].
Hatzi, Katerina ;
Jiang, Yanwen ;
Huang, Chuanxin ;
Garrett-Bakelman, Francine ;
Gearhart, Micah D. ;
Giannopoulou, Eugenia G. ;
Zumbo, Paul ;
Kirouac, Kevin ;
Bhaskara, Srividya ;
Polo, Jose M. ;
Kormaksson, Matthias ;
MacKerell, Alexander D., Jr. ;
Xue, Fengtian ;
Mason, Christopher E. ;
Hiebert, Scott W. ;
Prive, Gilbert G. ;
Cerchietti, Leandro ;
Bardwell, Vivian J. ;
Elemento, Olivier ;
Melnick, Ari .
CELL REPORTS, 2013, 4 (03) :578-588
[14]   c-Maf activates the promoter and enhancer of the IL-21 gene, and TGF-β inhibits c-Maf-induced IL-21 production in CD4+ T cells [J].
Hiramatsu, Yukiko ;
Suto, Akira ;
Kashiwakuma, Daisuke ;
Kanari, Hiroko ;
Kagami, Shin-ichiro ;
Ikeda, Kei ;
Hirose, Koichi ;
Watanabe, Norihiko ;
Grusby, Michael J. ;
Iwamoto, Itsuo ;
Nakajima, Hiroshi .
JOURNAL OF LEUKOCYTE BIOLOGY, 2010, 87 (04) :703-712
[15]   The BCL-6 POZ domain and other POZ domains interact with the co-repressors N-CoR and SMRT [J].
Huynh, KD ;
Bardwell, VJ .
ONCOGENE, 1998, 17 (19) :2473-2484
[16]   The transcription factor BATF controls the global regulators of class-switch recombination in both B cells and T cells [J].
Ise, Wataru ;
Kohyama, Masako ;
Schraml, Barbara U. ;
Zhang, Tingting ;
Schwer, Bjoern ;
Basu, Uttiya ;
Alt, Frederick W. ;
Tang, Jun ;
Oltz, Eugene M. ;
Murphy, Theresa L. ;
Murphy, Kenneth M. .
NATURE IMMUNOLOGY, 2011, 12 (06) :536-U245
[17]   The Transcription Factor T-bet Limits Amplification of Type I IFN Transcriptome and Circuitry in T Helper 1 Cells [J].
Iwata, Shigeru ;
Mikami, Yohei ;
Sun, Hong-Wei ;
Brooks, Stephen R. ;
Jankovic, Dragana ;
Hirahara, Kiyoshi ;
Onodera, Atsushi ;
Shih, Han-Yu ;
Kawabe, Takeshi ;
Jiang, Kan ;
Nakayama, Toshinori ;
Sher, Alan ;
O'Shea, John J. ;
Davis, Fred P. ;
Kanno, Yuka .
IMMUNITY, 2017, 46 (06) :983-+
[18]   Interleukin-23-Induced Transcription Factor Blimp-1 Promotes Pathogenicity of T Helper 17 Cells [J].
Jain, Renu ;
Chen, Yi ;
Kanno, Yuka ;
Joyce-Shaikh, Barbara ;
Vahedi, Golnaz ;
Hirahara, Kiyoshi ;
Blumenschein, Wendy M. ;
Sukumar, Selvakumar ;
Haines, Christopher J. ;
Sadekova, Svetlana ;
McClanahan, Terrill K. ;
McGeachy, Mandy J. ;
O'Shea, John J. ;
Cua, Daniel J. .
IMMUNITY, 2016, 44 (01) :131-142
[19]   STAT5 is a potent negative regulator of TFH cell differentiation [J].
Johnston, Robert J. ;
Choi, Youn Soo ;
Diamond, Jeffrey A. ;
Yang, Jessica A. ;
Crotty, Shane .
JOURNAL OF EXPERIMENTAL MEDICINE, 2012, 209 (02) :243-250
[20]   Bcl6 and Blimp-1 Are Reciprocal and Antagonistic Regulators of T Follicular Helper Cell Differentiation [J].
Johnston, Robert J. ;
Poholek, Amanda C. ;
DiToro, Daniel ;
Yusuf, Isharat ;
Eto, Danelle ;
Barnett, Burton ;
Dent, Alexander L. ;
Craft, Joe ;
Crotty, Shane .
SCIENCE, 2009, 325 (5943) :1006-1010