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.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Apoptosis / genetics
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Apoptosis / immunology
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Bone Marrow Transplantation
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Cell Differentiation / genetics
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Cell Differentiation / immunology
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Embryonic and Fetal Development / genetics
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Embryonic and Fetal Development / immunology
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Female
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Gene Expression Regulation, Developmental / immunology
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Injections, Intralymphatic
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Janus Kinase 3
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Kinetics
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Lymphopenia / enzymology
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Lymphopenia / genetics*
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Lymphopenia / immunology*
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Lymphopenia / pathology
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Male
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Mice
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Mice, Congenic
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Mice, Inbred C57BL
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Mice, Knockout
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Protein-Tyrosine Kinases / deficiency*
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Protein-Tyrosine Kinases / genetics*
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Protein-Tyrosine Kinases / physiology
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Signal Transduction / genetics
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Signal Transduction / immunology
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Stem Cells / enzymology*
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Stem Cells / immunology*
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Stem Cells / pathology
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Thymus Gland / enzymology*
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Thymus Gland / immunology*
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Thymus Gland / pathology
Substances
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Protein-Tyrosine Kinases
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Jak3 protein, mouse
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Janus Kinase 3