Regulation of the Development and Function of B Cells by ZBTB Transcription Factors

被引:49
作者
Zhu, Can [1 ]
Chen, Ge [1 ]
Zhao, Ying [2 ]
Gao, Xiao-Ming [1 ]
Wang, Jun [1 ]
机构
[1] Soochow Univ, Inst Biol & Med Sci, Suzhou, Peoples R China
[2] Soochow Univ, Dept Pathophysiol, Sch Biol & Basic Med Sci, Suzhou, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2018年 / 9卷
关键词
B cells; BCL6; ZBTB7A; ZBTB17; ZBTB20; ZBTB32; ZBTB1; ZBTB24; ZINC-FINGER PROTEIN; GERMINAL CENTER; PLASMA-CELL; ICF SYNDROME; LYMPHOCYTE DEVELOPMENT; FACTOR MIZ-1; CENTROMERIC INSTABILITY; MUTATIONAL ANALYSIS; LINEAGE COMMITMENT; GENE-EXPRESSION;
D O I
10.3389/fimmu.2018.00580
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 large ZBTB family comprises a diverse group of transcriptional factors. Several ZBTB proteins have emerged as critical factors that regulate the lineage commitment, differentiation, and function of lymphoid cells as well as many other developmental events. For instance, dysfunctions of ZBTB20 or ZBTB24 have been linked to multisystem failures in humans. Within the B-cell lineage, BCL6, ZBTB7A, ZBTB17, and ZBTB1 regulate the development/differentiation of B cells in both bone marrow and peripheral lymphoid organs, while ZBTB20 and ZBTB32 seem to mainly impact the maintenance of terminal plasma cells. Given the importance of B cells in the prevention and treatment of infectious or autoimmune disorders, we herein summarize the roles of seven ZBTB family members (BCL6, ZBTB7A, ZBTB17, ZBTB20, ZBTB32, ZBTB1, and ZBTB24) in the development, differentiation, and function of B cells as well as the underlying molecular mechanisms.
引用
收藏
页数:8
相关论文
共 77 条
[1]   Miz1 is required for early embryonic development during gastrulation [J].
Adhikary, S ;
Peukert, K ;
Karsunky, H ;
Beuger, V ;
Lutz, W ;
Elsässer, HP ;
Möröy, T ;
Eilers, M .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (21) :7648-7657
[2]   IDENTIFICATION OF THE GENE ASSOCIATED WITH THE RECURRING CHROMOSOMAL TRANSLOCATIONS T(3,14)(Q27,Q32) AND T(3,22)(Q27,Q11) IN B-CELL LYMPHOMAS [J].
BARON, BW ;
NUCIFORA, G ;
MCCABE, N ;
ESPINOSA, R ;
LEBEAU, MM ;
MCKEITHAN, TW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :5262-5266
[3]   Roles of BCL6 in normal and transformed germinal center B cells [J].
Basso, Katia ;
Dalla-Favera, Riccardo .
IMMUNOLOGICAL REVIEWS, 2012, 247 :172-183
[4]   The BTB-ZF Family of Transcription Factors: Key Regulators of Lineage Commitment and Effector Function Development in the Immune System [J].
Beaulieu, Aimee M. ;
Sant'Angelo, Derek B. .
JOURNAL OF IMMUNOLOGY, 2011, 187 (06) :2841-2847
[5]   In vivo cell biology:: following the zebrafish trend [J].
Beis, D ;
Stainier, DYR .
TRENDS IN CELL BIOLOGY, 2006, 16 (02) :105-112
[6]   Defective B-cell-negative selection and terminal differentiation in the ICF syndrome [J].
Blanco-Betancourt, CE ;
Moncla, A ;
Milili, M ;
Jiang, YL ;
Viegas-Péquignot, EM ;
Roquelaure, B ;
Thuret, I ;
Schiff, C .
BLOOD, 2004, 103 (07) :2683-2690
[7]   Zbtb1 Safeguards Genome Integrity and Prevents p53-Mediated Apoptosis in Proliferating Lymphoid Progenitors [J].
Cao, Xin ;
Lu, Ying ;
Zhang, Xianyu ;
Kovalovsky, Damian .
JOURNAL OF IMMUNOLOGY, 2016, 197 (04) :1199-1211
[8]   A Microarray Platform-Independent Classification Tool for Cell of Origin Class Allows Comparative Analysis of Gene Expression in Diffuse Large B-cell Lymphoma [J].
Care, Matthew A. ;
Barrans, Sharon ;
Worrillow, Lisa ;
Jack, Andrew ;
Westhead, David R. ;
Tooze, Reuben M. .
PLOS ONE, 2013, 8 (02)
[9]   The transcription factors IRF8 and PU.1 negatively regulate plasma cell differentiation [J].
Carotta, Sebastian ;
Willis, Simon N. ;
Hasbold, Jhagvaral ;
Inouye, Michael ;
Pang, Swee Heng Milon ;
Emslie, Dianne ;
Light, Amanda ;
Chopin, Michael ;
Shi, Wei ;
Wang, Hongsheng ;
Morse, Herbert C., III ;
Tarlinton, David M. ;
Corcoran, Lynn M. ;
Hodgkin, Philip D. ;
Nutt, Stephen L. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2014, 211 (11) :2169-2181
[10]   The BTB-ZF transcription factor Zbtb20 is driven by Irf4 to promote plasma cell differentiation and longevity [J].
Chevrier, Stephane ;
Emslie, Dianne ;
Shi, Wei ;
Kratina, Tobias ;
Wellard, Cameron ;
Karnowski, Alexander ;
Erikci, Erdem ;
Smyth, Gordon K. ;
Chowdhury, Kamal ;
Tarlinton, David ;
Corcoran, Lynn M. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2014, 211 (05) :827-840