BCL-6 represses genes that function in lymphocyte differentiation, inflammation, and cell cycle control

被引:680
作者
Shaffer, AL [1 ]
Yu, X [1 ]
He, YS [1 ]
Boldrick, J [1 ]
Chan, EP [1 ]
Staudt, LM [1 ]
机构
[1] NCI, Metab Branch, Div Clin Sci, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S1074-7613(00)00020-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BCL-6, a transcriptional repressor frequently translocated in lymphomas, regulates germinal center B cell differentiation and inflammation. DNA microarray screening identified genes repressed by BCL-6, including many lymphocyte activation genes, suggesting that BCL-6 modulates B cell receptor signals. BCL-6 repression of two chemokine genes, MIP-1 alpha and IP-10, may also attenuate inflammatory responses. Blimp-1, another BCL-6 target, is important for plasmacytic differentiation. Since BCL-6 expression is silenced in plasma cells, repression of blimp-1 by BCL-6 may control plasmacytic differentiation. Indeed, inhibition of BCL-6 function initiated changes indicative of plasmacytic differentiation, including decreased expression of c-Myc and increased expression of the cell cycle inhibitor p27kip1. These data suggest that malignant transformation by BCL-6 involves inhibition of differentiation and enhanced proliferation.
引用
收藏
页码:199 / 212
页数:14
相关论文
共 52 条
  • [1] The lymphochip: A specialized cDNA microarray for the genomic-scale analysis of gene expression in normal and malignant lymphocytes
    Alizadeh, A
    Eisen, M
    Davis, RE
    Ma, C
    Sabet, H
    Tran, T
    Powell, JI
    Yang, L
    Marti, GE
    Moore, DT
    Hudson, JR
    Chan, WC
    Greiner, T
    Weisenburger, D
    Armitage, JO
    Lossos, I
    Levy, R
    Botstein, D
    Brown, PO
    Staudt, LM
    [J]. COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1999, 64 : 71 - 78
  • [2] Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling
    Alizadeh, AA
    Eisen, MB
    Davis, RE
    Ma, C
    Lossos, IS
    Rosenwald, A
    Boldrick, JG
    Sabet, H
    Tran, T
    Yu, X
    Powell, JI
    Yang, LM
    Marti, GE
    Moore, T
    Hudson, J
    Lu, LS
    Lewis, DB
    Tibshirani, R
    Sherlock, G
    Chan, WC
    Greiner, TC
    Weisenburger, DD
    Armitage, JO
    Warnke, R
    Levy, R
    Wilson, W
    Grever, MR
    Byrd, JC
    Botstein, D
    Brown, PO
    Staudt, LM
    [J]. NATURE, 2000, 403 (6769) : 503 - 511
  • [3] BCL-6 expression during B-cell activation
    Allman, D
    Jain, A
    Dent, A
    Maile, RR
    Selvaggi, T
    Kehry, MR
    Staudt, LM
    [J]. BLOOD, 1996, 87 (12) : 5257 - 5268
  • [4] BARONI M, 1995, PROG VET NEUROL, V6, P13
  • [5] Briegel K, 1996, DEVELOPMENT, V122, P3839
  • [6] HIGH-LEVELS OF CD44 EXPRESSION DISTINGUISH VIRGIN FROM ANTIGEN-PRIMED B-CELLS
    CAMP, RL
    KRAUS, TA
    BIRKELAND, ML
    PURE, E
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (03) : 763 - 766
  • [7] Carman JA, 1996, J IMMUNOL, V156, P4562
  • [8] BCL-6 PROTEIN IS EXPRESSED IN GERMINAL-CENTER B-CELLS
    CATTORETTI, G
    CHANG, CC
    CECHOVA, K
    ZHANG, JD
    YE, BH
    FALINI, B
    LOUIE, DC
    OFFIT, K
    CHAGANTI, RSK
    DALLAFAVERA, R
    [J]. BLOOD, 1995, 86 (01) : 45 - 53
  • [9] INTERACTION OF PROTEINS WITH TRANSCRIPTIONALLY ACTIVE ESTROGEN-RECEPTORS
    CAVAILLES, V
    DAUVOIS, S
    DANIELIAN, PS
    PARKER, MG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (21) : 10009 - 10013
  • [10] REQUIREMENT OF MIP-1-ALPHA FOR AN INFLAMMATORY RESPONSE TO VIRAL-INFECTION
    COOK, DN
    BECK, MA
    COFFMAN, TM
    KIRBY, SL
    SHERIDAN, JF
    PRAGNELL, IB
    SMITHIES, O
    [J]. SCIENCE, 1995, 269 (5230) : 1583 - 1585