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The Journal of Immunology, 2004, 173: 2307-2314.
Copyright © 2004 by The American Association of Immunologists

STAT5 Is Required for Thymopoiesis in a Development Stage-Specific Manner1

Joonsoo Kang2,*, Brian DiBenedetto*, Kavitha Narayan*, Hang Zhao*, Sandy D. Der{dagger} and Cynthia A. Chambers*

* Department of Pathology, Graduate Program in Immunology and Virology, University of Massachusetts Medical School, Worcester, MA 01655; and {dagger} Department of Laboratory Medicine and Pathobiology, Program in Proteomics and Bioinformatics, University of Toronto, Toronto, Ontario, Canada

Diverse cytokines necessary for normal lymphopoiesis and lymphocyte homeostasis activate STAT5 in responder cells. Although STAT5 has been suggested to be a central molecular effecter of IL-7 function, its essential role during IL-7-dependent T cell development in vivo remained unclear. Using Stat5–/– mice we now show that STAT5 is essential for various functions ascribed to IL-7 in vivo. STAT5 is required for embryonic thymocyte production, TCR{gamma} gene transcription, and Peyer’s patch development. In sharp contrast, normal STAT5 is dispensable for adult thymopoiesis. In peripheral lymphocytes, STAT5 is primarily required for the generation and/or maintenance of {gamma}{delta} T cells and TCR{gamma}{delta}+ intraepithelial lymphocytes. Collectively, these results demonstrate that STAT5 is critical for many, but not all, aspects of steady state lymphoid lineage development and maintenance and suggest the existence of previously undocumented cytokine signaling traits and/or cytokine milieu during adult thymopoiesis.


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