Blimp-1-dependent repression of Pax-5 is required for differentiation of B cells to immunoglobulin M-secreting plasma cells

被引:350
作者
Lin, KI [1 ]
Angelin-Duclos, C [1 ]
Kuo, TC [1 ]
Calame, K [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Microbiol, New York, NY 10032 USA
关键词
D O I
10.1128/MCB.22.13.4771-4780.2002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
B-cell lineage-specific activator protein (BSAP), encoded by the Pax-5 gene, is critical for B-cell lineage commitment and B-cell development but is not expressed in terminally differentiated B cells. We demonstrate a direct connection between BSAP and B-lymphocyte-induced maturation protein 1 (Blimp-1), a transcriptional repressor that is sufficient to drive plasmacytic differentiation. Blimp-1 binds a site on the Pax-5 promoter in vitro and in vivo and represses the Pax-5 promoter in a binding-site-dependent manner. By ectopically expressing Blimp-1 or a competitive inhibitor of Blimp-1, we show that Blimp-1 is both necessary and sufficient to repress Pax-5 during plasmacytic differentiation of primary splenic B cells. Blimp-1-dependent repression of Pax-5 is sufficient to regulate BSAP targets CD19 and J chain and is necessary but not sufficient to induce XBP-1. We further show that repression of Pax-5 is required for Blimp-1 to drive differentiation of splenocytes to immunoglobulin M-secreting cells. Thus, repression of Pax-5 plays a critical role in the Blimp-1-dependent program of plasmacytic differentiation.
引用
收藏
页码:4771 / 4780
页数:10
相关论文
共 35 条
[1]   PAX-5 ENCODES THE TRANSCRIPTION FACTOR BSAP AND IS EXPRESSED IN LYMPHOCYTES-B, THE DEVELOPING CNS, AND ADULT TESTIS [J].
ADAMS, B ;
DORFLER, P ;
AGUZZI, A ;
KOZMIK, Z ;
URBANEK, P ;
MAURERFOGY, I ;
BUSSLINGER, M .
GENES & DEVELOPMENT, 1992, 6 (09) :1589-1607
[2]   Commitment of B lymphocytes to a plasma cell fate is associated with Blimp-1 expression in vivo [J].
Angelin-Duclos, C ;
Cattoretti, G ;
Lin, KI ;
Calame, K .
JOURNAL OF IMMUNOLOGY, 2000, 165 (10) :5462-5471
[3]   Role of B-lymphocyte-induced maturation protein-1 in terminal differentiation of B cells and other cell lineages [J].
Angelin-Duclos, C ;
Cattoretti, G ;
Chang, DH ;
Lin, KI ;
Lin, Y ;
Yu, J ;
Calame, K .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1999, 64 :61-70
[4]   A NOVEL B-CELL LINEAGE-SPECIFIC TRANSCRIPTION FACTOR PRESENT AT EARLY BUT NOT LATE STAGES OF DIFFERENTIATION [J].
BARBERIS, A ;
WIDENHORN, K ;
VITELLI, L ;
BUSSLINGER, M .
GENES & DEVELOPMENT, 1990, 4 (05) :849-859
[5]   BLIMP-I: trigger for differentiation of myeloid lineage [J].
Chang, DH ;
Angelin-Duclos, C ;
Calame, K .
NATURE IMMUNOLOGY, 2000, 1 (02) :169-176
[6]   ONLY 2 OF THE 5 ZINC FINGERS OF THE EUKARYOTIC TRANSCRIPTIONAL REPRESSOR PRDI-BF1 ARE REQUIRED FOR SEQUENCE-SPECIFIC DNA-BINDING [J].
KELLER, AD ;
MANIATIS, T .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (05) :1940-1949
[7]   IDENTIFICATION AND CHARACTERIZATION OF A NOVEL REPRESSOR OF INTERFERON-BETA GENE-EXPRESSION [J].
KELLER, AD ;
MANIATIS, T .
GENES & DEVELOPMENT, 1991, 5 (05) :868-879
[8]   THE PROMOTER OF THE CD19 GENE IS A TARGET FOR THE B-CELL-SPECIFIC TRANSCRIPTION FACTOR BSAP [J].
KOZMIK, Z ;
WANG, S ;
DORFLER, P ;
ADAMS, B ;
BUSSLINGER, M .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (06) :2662-2672
[9]   Repression of c-myc is necessary but not sufficient for terminal differentiation of B lymphocytes in vitro [J].
Lin, KI ;
Lin, Y ;
Calame, K .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (23) :8684-8695
[10]   Repression of c-myc transcription by blimp-1, an inducer of terminal B cell differentiation [J].
Lin, Y ;
Wong, KK ;
Calame, K .
SCIENCE, 1997, 276 (5312) :596-599