Abstract
The divergence of alphabeta and gammadelta T cells from a common precursor in the thymus is regulated by multiple cell-intrinsic and cell-extrinsic factors, most of which are not well defined. Recent studies have provided crucial data regarding the precise timing of lineage commitment and some clarification on the extent of the involvement of Notch and T-cell receptor signaling in this process. Combined with new insights into the differential regulation of molecular pathways active in alphabeta and gammadelta precursors, these data have led to the generation of a revised model of lineage commitment.
Publication types
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Research Support, N.I.H., Extramural
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Review
MeSH terms
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Animals
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Cell Lineage / genetics
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Lymphopoiesis* / genetics
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Mice
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Multipotent Stem Cells / chemistry
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Multipotent Stem Cells / immunology*
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Receptors, Antigen, T-Cell, alpha-beta / analysis
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Receptors, Antigen, T-Cell, alpha-beta / metabolism*
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Receptors, Antigen, T-Cell, gamma-delta / analysis
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Receptors, Antigen, T-Cell, gamma-delta / metabolism*
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Receptors, Notch / physiology
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T-Lymphocytes / immunology*
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Thymus Gland / cytology
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Thymus Gland / immunology*
Substances
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Receptors, Antigen, T-Cell, alpha-beta
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Receptors, Antigen, T-Cell, gamma-delta
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Receptors, Notch