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    PTPN2 regulates T cell lineage commitment and alpha beta versus gamma delta specification

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    Author
    Wiede, F; Dudakov, JA; Lu, K-H; Dodd, GT; Butt, T; Godfrey, DI; Strasser, A; Boyd, RL; Tiganis, T
    Date
    2017-09-01
    Source Title
    Journal of Experimental Medicine
    Publisher
    ROCKEFELLER UNIV PRESS
    University of Melbourne Author/s
    Tiganis, Tony; Godfrey, Dale; Strasser, Andreas; Dodd, Garron
    Affiliation
    Microbiology and Immunology
    Medical Biology (W.E.H.I.)
    Sir Peter MacCallum Department of Oncology
    Physiology
    Metadata
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    Document Type
    Journal Article
    Citations
    Wiede, F., Dudakov, J. A., Lu, K. -H., Dodd, G. T., Butt, T., Godfrey, D. I., Strasser, A., Boyd, R. L. & Tiganis, T. (2017). PTPN2 regulates T cell lineage commitment and alpha beta versus gamma delta specification. JOURNAL OF EXPERIMENTAL MEDICINE, 214 (9), pp.2733-2758. https://doi.org/10.1084/jem.20161903.
    Access Status
    Open Access
    URI
    http://hdl.handle.net/11343/256744
    DOI
    10.1084/jem.20161903
    Abstract
    In the thymus, hematopoietic progenitors commit to the T cell lineage and undergo sequential differentiation to generate diverse T cell subsets, including major histocompatibility complex (MHC)-restricted αβ T cell receptor (TCR) T cells and non-MHC-restricted γδ TCR T cells. The factors controlling precursor commitment and their subsequent maturation and specification into αβ TCR versus γδ TCR T cells remain unclear. Here, we show that the tyrosine phosphatase PTPN2 attenuates STAT5 (signal transducer and activator of transcription 5) signaling to regulate T cell lineage commitment and SRC family kinase LCK and STAT5 signaling to regulate αβ TCR versus γδ TCR T cell development. Our findings identify PTPN2 as an important regulator of critical checkpoints that dictate the commitment of multipotent precursors to the T cell lineage and their subsequent maturation into αβ TCR or γδ TCR T cells.

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