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

被引:350
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
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