The proto-oncogene MYC is required for selection in the germinal center and cyclic reentry

被引:354
作者
Dominguez-Sola, David [1 ]
Victora, Gabriel D. [2 ]
Ying, Carol Y. [1 ]
Phan, Ryan T. [1 ]
Saito, Masumichi [1 ]
Nussenzweig, Michel C. [2 ,3 ]
Dalla-Favera, Riccardo [1 ,4 ,5 ,6 ,7 ]
机构
[1] Columbia Univ, Inst Canc Genet, New York, NY 10027 USA
[2] Rockefeller Univ, Lab Mol Immunol, New York, NY 10021 USA
[3] Howard Hughes Med Inst, New York, NY USA
[4] Columbia Univ, Herbert Irving Comprehens Canc Ctr, New York, NY USA
[5] Columbia Univ, Dept Pathol & Cell Biol, New York, NY USA
[6] Columbia Univ, Dept Genet & Dev, New York, NY USA
[7] Columbia Univ, Dept Microbiol & Immunol, New York, NY USA
基金
美国国家卫生研究院;
关键词
CENTER B-CELLS; RESPONSES IN-VIVO; T-CELL; C-MYC; IMMUNE-RESPONSE; AFFINITY MATURATION; EXPRESSION; BCL6; ACTIVATION; DYNAMICS;
D O I
10.1038/ni.2428
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
After antigenic challenge, B cells enter the dark zone (DZ) of germinal centers (GCs) to proliferate and hypermutate their immunoglobulin genes. Mutants with greater affinity for the antigen are positively selected in the light zone (LZ) to either differentiate into plasma and memory cells or reenter the DZ. The molecular circuits that govern positive selection in the GC are not known. We show here that the GC reaction required biphasic regulation of expression of the cell-cycle regulator c-Myc that involved its transient induction during early GC commitment, its repression by Bcl-6 in DZ B cells and its reinduction in B cells selected for reentry into the DZ. Inhibition of c-Myc in vivo led to GC collapse, which indicated an essential role for c-Myc in GCs. Our results have implications for the mechanism of GC selection and the role of c-Myc in lymphomagenesis.
引用
收藏
页码:1083 / 1091
页数:9
相关论文
共 51 条
[1]   Germinal-center organization and cellular dynamics [J].
Allen, Christopher D. C. ;
Okada, Takaharu ;
Cyster, Jason G. .
IMMUNITY, 2007, 27 (02) :190-202
[2]   Imaging of germinal center selection events during affinity maturation [J].
Allen, Christopher D. C. ;
Okada, Takaharu ;
Tang, H. Lucy ;
Cyster, Jason G. .
SCIENCE, 2007, 315 (5811) :528-531
[3]  
[Anonymous], NAT IMMUNOL, DOI DOI 10.1038/ni.2242
[4]   Roles of BCL6 in normal and transformed germinal center B cells [J].
Basso, Katia ;
Dalla-Favera, Riccardo .
IMMUNOLOGICAL REVIEWS, 2012, 247 :172-183
[5]   Integrated biochemical and computational approach identifies BCL6 direct target genes controlling multiple pathways in normal germinal center B cells [J].
Basso, Katia ;
Saito, Masumichi ;
Sumazin, Pavel ;
Margolin, Adam A. ;
Wang, Kai ;
Lim, Wei-Keat ;
Kitagawa, Yukiko ;
Schneider, Christof ;
Alvarez, Mariano J. ;
Califano, Andrea ;
Dalla-Favera, Riccardo .
BLOOD, 2010, 115 (05) :975-984
[6]   B cells acquire antigen from target cells after synapse formation [J].
Batista, FD ;
Iber, D ;
Neuberger, MS .
NATURE, 2001, 411 (6836) :489-494
[7]   Acetylation inactivates the transcriptional repressor BCL6 [J].
Bereshchenko, OR ;
Gu, W ;
Dalla-Favera, R .
NATURE GENETICS, 2002, 32 (04) :606-613
[8]   CD27 and CD70 in T cell and B cell activation [J].
Borst, J ;
Hendriks, J ;
Xiao, YL .
CURRENT OPINION IN IMMUNOLOGY, 2005, 17 (03) :275-281
[9]   Nuclear and cytoplasmic AID in extrafollicular and germinal center B cells [J].
Cattoretti, Giorgio ;
Buettner, Maike ;
Shaknovich, Rita ;
Kremmer, Elisabeth ;
Alobeid, Bachir ;
Niedobitek, Gerald .
BLOOD, 2006, 107 (10) :3967-3975
[10]   The BCL6 transcriptional program features repression of multiple oncogenes in primary B cells and is deregulated in DLBCL [J].
Ci, Weimin ;
Polo, Jose M. ;
Cerchietti, Leandro ;
Shaknovich, Rita ;
Wang, Ling ;
Yang, Shao Ning ;
Ye, Kenny ;
Farinha, Pedro ;
Horsman, Douglas E. ;
Gascoyne, Randy D. ;
Elemento, Olivier ;
Melnick, Ari .
BLOOD, 2009, 113 (22) :5536-5548