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    A profound deficiency in thymic progenitor cells in mice lacking Jak3

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    Authors
    Baird, Allison Michelle
    Lucas, Julie Ann
    Berg, Leslie J.
    UMass Chan Affiliations
    Department of Pathology
    Graduate School of Biomedical Sciences
    Document Type
    Journal Article
    Publication Date
    2000-10-18
    Keywords
    Animals; Apoptosis; Bone Marrow Transplantation; Cell Differentiation; Embryonic and Fetal Development; Female; Gene Expression Regulation, Developmental; Injections, Intralymphatic; Janus Kinase 3; Kinetics; Lymphopenia; Male; Mice; Mice, Congenic; Mice, Inbred C57BL; Mice, Knockout; Protein-Tyrosine Kinases; Signal Transduction; Stem Cells; Thymus Gland
    Life Sciences
    Medicine and Health Sciences
    
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    Link to Full Text
    https://doi.org/10.4049/jimmunol.165.7.3680
    Abstract
    Humans and mice with genetic deficiencies that lead to loss of signaling through common gamma-chain (gammac)-containing cytokine receptors have severe defects in B and T lymphocytes. In humans, these deficiencies lead to a complete absence of T cells, whereas in mice, small thymuses give rise to normal numbers of peripheral T cells. We have examined the first wave of developing T cells in Jak3-/-, IL-7-/-, and IL-7Ralpha-/- fetal mice, and have found a near absence of thymic progenitor cells. This deficiency is highlighted by the complete inability of Jak3-/- progenitor cells to reconstitute T cell development in the presence of competing wild-type cells. These data clearly demonstrate a strong common basis for the T cell deficiencies in mice and humans lacking gammac/Jak3 signaling pathways.
    Source

    J Immunol. 2000 Oct 1;165(7):3680-8.

    DOI
    10.4049/jimmunol.165.7.3680
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/34029
    PubMed ID
    11034372
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    Link to article in PubMed

    ae974a485f413a2113503eed53cd6c53
    10.4049/jimmunol.165.7.3680
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