Stat5 Synergizes with T Cell Receptor/Antigen Stimulation in the Development of Lymphoblastic Lymphoma

Author:

Kelly John A.1,Spolski Rosanne1,Kovanen Panu E.1,Suzuki Takeshi2,Bollenbacher Julie1,Pise-Masison Cynthia A.2,Radonovich Michael F.3,Lee Stephen1,Jenkins Nancy A.2,Copeland Neal G.2,Morse Herbert C.4,Leonard Warren J.1

Affiliation:

1. Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute

2. Mouse Cancer Genetics Program, National Cancer Institute-Frederick, Frederick, MD 21702

3. Laboratory of Receptor Biology and Gene Expression, National Cancer Institute, Bethesda, MD 20892

4. The Laboratory of Immunopathology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852

Abstract

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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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