Stat5 synergizes with T cell receptor/antigen stimulation in the development of lymphoblastic lymphoma

被引:66
作者
Kelly, JA
Spolski, R
Kovanen, PE
Suzuki, T
Bollenbacher, J
Pise-Masison, CA
Radonovich, MF
Lee, S
Jenkins, NA
Copeland, NG
Morse, HC
Leonard, WJ
机构
[1] NHLBI, Lab Mol Immunol, NIH, Bethesda, MD 20892 USA
[2] NCI, Lab Receptor Biol & Gene Express, Bethesda, MD 20892 USA
[3] NCI, Frederick Canc Res & Dev Ctr, Mouse Canc Genet Program, Frederick, MD 21702 USA
[4] NIAID, Immunopathol Lab, NIH, Rockville, MD 20852 USA
关键词
Stat5; TCR; lymphoma; DNA microarray; CD8(+)T cell;
D O I
10.1084/jem.20021548
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Signal transducer and activator of transcription (STAT) proteins are latent transcription factors that mediate a wide range of actions induced by cytokines, interferons, and growth factors. We now report the development of thymic T cell lymphoblastic lymphomas in transgenic mice in which Stat5a or Stat5b is overexpressed within the lymphoid compartment. The rate of lymphoma induction was markedly enhanced by immunization or by the introduction of TCR transgenes. Remarkably, the Stat5 transgene potently induced development of CD8(+) T cells, even in mice expressing a class II-restricted TCR transgene, with resulting CD8(+) T cell lymphomas. These data demonstrate the oncogenic potential of dysregulated expression of a STAT protein that is not constitutively activated, and that TCR stimulation can contribute to this process.
引用
收藏
页码:79 / 89
页数:11
相关论文
共 42 条
[1]  
Billiau A, 2001, J LEUKOCYTE BIOL, V70, P849
[2]   STATs in oncogenesis [J].
Bowman, T ;
Garcia, R ;
Turkson, J ;
Jove, R .
ONCOGENE, 2000, 19 (21) :2474-2488
[3]   Stat3 as an oncogene [J].
Bromberg, JF ;
Wrzeszczynska, MH ;
Devgan, G ;
Zhao, YX ;
Pestell, RG ;
Albanese, C ;
Darnell, JE .
CELL, 1999, 98 (03) :295-303
[4]   Coreceptor reversal in the thymus:: Signaled CD4+8+ thymocytes initially terminate CD8 transcription even when differentiating into CD8+ T cells [J].
Brugnera, E ;
Bhandoola, A ;
Cibotti, R ;
Yu, Q ;
Guinter, TI ;
Yamashita, Y ;
Sharrow, SO ;
Singer, A .
IMMUNITY, 2000, 13 (01) :59-71
[5]   How Stat1 mediates constitutive gene expression: a complex of unphosphorylated Stat1 and IRF1 supports transcription of the LMP2 gene [J].
Chatterjee-Kishore, M ;
Wright, KL ;
Ting, JPY ;
Stark, GR .
EMBO JOURNAL, 2000, 19 (15) :4111-4122
[6]   CHARACTERIZATION OF A PROTEIN-TYROSINE-PHOSPHATASE (RIP) EXPRESSED AT A VERY EARLY-STAGE OF DIFFERENTIATION IN BOTH MOUSE ERYTHROLEUKEMIA AND EMBRYONAL CARCINOMA-CELLS [J].
CHIDA, D ;
KUME, T ;
MUKOUYAMA, Y ;
TABATA, S ;
NOMURA, N ;
THOMAS, ML ;
WATANABE, T ;
OISHI, M .
FEBS LETTERS, 1995, 358 (03) :233-239
[7]   JAK-STAT SIGNALING INDUCED BY THE V-ABL ONCOGENE [J].
DANIAL, NN ;
PERNIS, A ;
ROTHMAN, PB .
SCIENCE, 1995, 269 (5232) :1875-1877
[8]   STATs and gene regulation [J].
Darnell, JE .
SCIENCE, 1997, 277 (5332) :1630-1635
[9]   Interactions of STAT5b-RARα, a novel acute promyelocytic leukemia fusion protein, with retinoic acid receptor and STAT3 signaling pathways [J].
Dong, S ;
Tweardy, DJ .
BLOOD, 2002, 99 (08) :2637-2646
[10]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868