Abstract
IL-7 plays an important role in the growth and differentiation of T cells. We have previously reported that IL-7 induces preferential expansion of MHC class I-selected CD4-CD8-TCR alpha beta+ thymocytes which express a skewed V beta repertoire and are potent IL-4 producers. In this report, we provide evidence that IL-1 in combination with granulocyte macrophage colony stimulating factor can also expand this population. Yet, these cells do not share the functional characteristics of those obtained in the presence of IL-7, i.e. cytotoxic activity and high IL-4 production. These functional capacities can be acquired by adding IL-7. In conclusion, our findings demonstrate that the capacity of MHC class I-selected CD4-CD8-TCR alpha beta+ thymocytes to produce IL-4 as well as to kill target cells is IL-7 dependent.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antibodies, Monoclonal / pharmacology
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CD3 Complex / immunology
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CD4 Antigens / analysis*
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CD8 Antigens / analysis*
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Cells, Cultured
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Cytotoxicity, Immunologic / drug effects
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Drug Combinations
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Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
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H-2 Antigens / immunology*
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Interleukin-1 / pharmacology
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Interleukin-4 / biosynthesis*
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Interleukin-7 / physiology*
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Lymphocyte Activation / drug effects
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Mice
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Mice, Inbred C3H
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Mice, Mutant Strains
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Receptors, Antigen, T-Cell, alpha-beta / analysis*
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T-Lymphocyte Subsets / drug effects
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T-Lymphocyte Subsets / metabolism*
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Thymus Gland / cytology
Substances
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Antibodies, Monoclonal
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CD3 Complex
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CD4 Antigens
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CD8 Antigens
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Drug Combinations
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H-2 Antigens
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Interleukin-1
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Interleukin-7
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Receptors, Antigen, T-Cell, alpha-beta
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Interleukin-4
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Granulocyte-Macrophage Colony-Stimulating Factor