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NK T Cell Precursors Exhibit Differential Cytokine Regulation and Require Itk for Efficient Maturation

NK T cells are a lymphocyte lineage that is selected by CD1d and is characterized by the ability to rapidly secrete large amounts of both IFN-gamma and IL-4 after TCR stimulation. Using reactivity to CD1d tetramers to define presumptive NK T cells, several NK T cell progenitor populations were chara...

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Published in:The Journal of immunology (1950) 2002-09, Vol.169 (5), p.2397-2406
Main Authors: Gadue, Paul, Stein, Paul L
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Language:English
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Stein, Paul L
description NK T cells are a lymphocyte lineage that is selected by CD1d and is characterized by the ability to rapidly secrete large amounts of both IFN-gamma and IL-4 after TCR stimulation. Using reactivity to CD1d tetramers to define presumptive NK T cells, several NK T cell progenitor populations were characterized based upon NK marker expression and CD4 vs CD8 expression. The earliest populations were found to be negative for NK markers and could proliferate to IL-7, while mature NK T cells did not. The NK1.1(-) NK T cell progenitors were capable of up-regulating NK1.1 when transferred in vivo. Upon stimulation, the NK1.1(-) populations secrete IL-4, but little IFN-gamma. As the cells mature and up-regulate NK1.1, they acquire the ability to secrete IFN-gamma. Finally, the Tec family tyrosine kinase Itk is necessary for optimal NK1.1 up-regulation and hence final maturation of NK T cells. The itk(-/-) mice also display a progressive decrease in NK T cells in older animals, suggesting a further role in peripheral maintenance.
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Using reactivity to CD1d tetramers to define presumptive NK T cells, several NK T cell progenitor populations were characterized based upon NK marker expression and CD4 vs CD8 expression. The earliest populations were found to be negative for NK markers and could proliferate to IL-7, while mature NK T cells did not. The NK1.1(-) NK T cell progenitors were capable of up-regulating NK1.1 when transferred in vivo. Upon stimulation, the NK1.1(-) populations secrete IL-4, but little IFN-gamma. As the cells mature and up-regulate NK1.1, they acquire the ability to secrete IFN-gamma. Finally, the Tec family tyrosine kinase Itk is necessary for optimal NK1.1 up-regulation and hence final maturation of NK T cells. 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source Free E-Journal (出版社公開部分のみ)
subjects Animals
Antigens - biosynthesis
Antigens, CD - biosynthesis
Antigens, Ly
Antigens, Surface - biosynthesis
CD4 Antigens - biosynthesis
CD8 Antigens - biosynthesis
Cell Differentiation - genetics
Cell Differentiation - immunology
Cell Division - genetics
Cell Division - immunology
Cytokines - biosynthesis
Cytokines - physiology
Immunophenotyping
Injections, Intravenous
Integrin alpha2
Interleukin-7 - pharmacology
Killer Cells, Natural - cytology
Killer Cells, Natural - enzymology
Killer Cells, Natural - immunology
Killer Cells, Natural - metabolism
Lectins, C-Type
Lymphocyte Transfusion
Mice
Mice, Inbred C57BL
Mice, Knockout
NK Cell Lectin-Like Receptor Subfamily B
Protein Biosynthesis
Protein-Tyrosine Kinases - deficiency
Protein-Tyrosine Kinases - genetics
Protein-Tyrosine Kinases - physiology
Proteins
Stem Cell Transplantation
Stem Cells - immunology
Stem Cells - metabolism
T-Lymphocyte Subsets - cytology
T-Lymphocyte Subsets - enzymology
T-Lymphocyte Subsets - immunology
T-Lymphocyte Subsets - metabolism
Time Factors
title NK T Cell Precursors Exhibit Differential Cytokine Regulation and Require Itk for Efficient Maturation
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