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.
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7 July 2003
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June 30 2003
Stat5 Synergizes with T Cell Receptor/Antigen Stimulation in the Development of Lymphoblastic Lymphoma
John A. Kelly,
John A. Kelly
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
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Rosanne Spolski,
Rosanne Spolski
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
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Panu E. Kovanen,
Panu E. Kovanen
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
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Takeshi Suzuki,
Takeshi Suzuki
3Mouse Cancer Genetics Program, National Cancer Institute-Frederick, Frederick, MD 21702
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Julie Bollenbacher,
Julie Bollenbacher
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
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Cynthia A. Pise-Masison,
Cynthia A. Pise-Masison
3Mouse Cancer Genetics Program, National Cancer Institute-Frederick, Frederick, MD 21702
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Michael F. Radonovich,
Michael F. Radonovich
2Laboratory of Receptor Biology and Gene Expression, National Cancer Institute, Bethesda, MD 20892
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Stephen Lee,
Stephen Lee
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
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Nancy A. Jenkins,
Nancy A. Jenkins
3Mouse Cancer Genetics Program, National Cancer Institute-Frederick, Frederick, MD 21702
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Neal G. Copeland,
Neal G. Copeland
3Mouse Cancer Genetics Program, National Cancer Institute-Frederick, Frederick, MD 21702
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Herbert C. Morse, III,
Herbert C. Morse, III
4The Laboratory of Immunopathology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852
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Warren J. Leonard
Warren J. Leonard
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
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John A. Kelly
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
Rosanne Spolski
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
Panu E. Kovanen
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
Takeshi Suzuki
3Mouse Cancer Genetics Program, National Cancer Institute-Frederick, Frederick, MD 21702
Julie Bollenbacher
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
Cynthia A. Pise-Masison
3Mouse Cancer Genetics Program, National Cancer Institute-Frederick, Frederick, MD 21702
Michael F. Radonovich
2Laboratory of Receptor Biology and Gene Expression, National Cancer Institute, Bethesda, MD 20892
Stephen Lee
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
Nancy A. Jenkins
3Mouse Cancer Genetics Program, National Cancer Institute-Frederick, Frederick, MD 21702
Neal G. Copeland
3Mouse Cancer Genetics Program, National Cancer Institute-Frederick, Frederick, MD 21702
Herbert C. Morse, III
4The Laboratory of Immunopathology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852
Warren J. Leonard
1Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute
Address correspondence to W.J. Leonard, Bldg. 10, Rm. 7N252, Laboratory of Molecular Immunology, NHLBI, NIH, Bethesda, MD 20892-1674. Phone: 301-496-0098; Fax: 301-402-0971; E-mail: [email protected]
The online version of this article contains supplemental material.
*
Abbreviations used in this paper: EMSA, electrophoretic mobility shift assay; STAT, signal transducer and activator of transcription.
Received:
September 03 2002
Revision Received:
April 23 2003
Accepted:
April 23 2003
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2003
J Exp Med (2003) 198 (1): 79–89.
Article history
Received:
September 03 2002
Revision Received:
April 23 2003
Accepted:
April 23 2003
Citation
John A. Kelly, Rosanne Spolski, Panu E. Kovanen, Takeshi Suzuki, Julie Bollenbacher, Cynthia A. Pise-Masison, Michael F. Radonovich, Stephen Lee, Nancy A. Jenkins, Neal G. Copeland, Herbert C. Morse, Warren J. Leonard; Stat5 Synergizes with T Cell Receptor/Antigen Stimulation in the Development of Lymphoblastic Lymphoma . J Exp Med 7 July 2003; 198 (1): 79–89. doi: https://doi.org/10.1084/jem.20021548
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