Regulation of T cell cytokine production by dendritic cells
Previous work has established that the dendritic cells (DC) of mouse spleen regulate the IL‐2 production, and hence the extent of proliferation, of the CD8 T cells they activate. It is now reported here that interaction of primary CD8 T cells with splenic CD8α DC induced much higher production of I...
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Published in | Immunology and cell biology Vol. 78; no. 3; pp. 214 - 223 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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United States
Nature Publishing Group
01.06.2000
Blackwell Science Ltd |
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Abstract | Previous work has established that the dendritic cells (DC) of mouse spleen regulate the IL‐2 production, and hence the extent of proliferation, of the CD8 T cells they activate. It is now reported here that interaction of primary CD8 T cells with splenic CD8α DC induced much higher production of IL‐3, IFN‐γ and granulocyte‐macrophage colony‐stimulating factor (GM‐CSF), as well as IL‐2, than did interaction with CD8α+ splenic DC. Furthermore, the CD8α DC also induced higher levels of IL‐2, IL‐3 and IL‐10 production in primary CD4 T cells, compared with that induced by CD8α+ DC. These quantitative differences did not involve qualitative shifts in the type of cytokine produced. Interleukin‐4 production remained low in all the primary T cell cultures and restimulation experiments in secondary cultures did not reveal any bias in the cytokine production profile. When exogenous IL‐2 was added to the primary cultures to ensure equal proliferation in response to CD8α or CD8α+ DC, the higher level of production of IL‐3, IFN‐γ and GM‐CSF induced by CD8α DC was maintained. Thus, this general control of T cell cytokine production by splenic DC involves factors additional to those that govern activation of T cells into cell cycle. |
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AbstractList | Previous work has established that the dendritic cells (DC) of mouse spleen regulate the IL-2 production, and hence the extent of proliferation, of the CD8 T cells they activate. It is now reported here that interaction of primary CD8 T cells with splenic CD8alpha- DC induced much higher production of IL-3, IFN-gamma and granulocyte-macrophage colony-stimulating factor (GM-CSF), as well as IL-2, than did interaction with CD8alpha+ splenic DC. Furthermore, the CD8alpha- DC also induced higher levels of IL-2, IL-3 and IL-10 production in primary CD4 T cells, compared with that induced by CD8alpha+ DC. These quantitative differences did not involve qualitative shifts in the type of cytokine produced. Interleukin-4 production remained low in all the primary T cell cultures and restimulation experiments in secondary cultures did not reveal any bias in the cytokine production profile. When exogenous IL-2 was added to the primary cultures to ensure equal proliferation in response to CD8alpha- or CD8alpha+ DC, the higher level of production of IL-3, IFN-gamma and GM-CSF induced by CD8alpha- DC was maintained. Thus, this general control of T cell cytokine production by splenic DC involves factors additional to those that govern activation of T cells into cell cycle. Previous work has established that the dendritic cells (DC) of mouse spleen regulate the IL-2 production, and hence the extent of proliferation, of the CD8 T cells they activate. It is now reported here that interaction of primary CD8 T cells with splenic CD8 alpha super(-) DC induced much higher production of IL-3, IFN- gamma and granulocyte-macrophage colony-stimulating factor (GM-CSF), as well as IL-2, than did interaction with CD8 alpha super(+) splenic DC. Furthermore, the CD8 alpha super(-) DC also induced higher levels of IL-2, IL-3 and IL-10 production in primary CD4 T cells, compared with that induced by CD8 alpha super(+) DC. These quantitative differences did not involve qualitative shifts in the type of cytokine produced. Interleukin-4 production remained low in all the primary T cell cultures and restimulation experiments in secondary cultures did not reveal any bias in the cytokine production profile. When exogenous IL-2 was added to the primary cultures to ensure equal proliferation in response to CD8 alpha super(-) or CD8 alpha super(+) DC, the higher level of production of IL-3, IFN- gamma and GM-CSF induced by CD8 alpha super(-) DC was maintained. Thus, this general control of T cell cytokine production by splenic DC involves factors additional to those that govern activation of T cells into cell cycle. SummaryPrevious work has established that the dendritic cells (DC) of mouse spleen regulate the IL-2 production, and hence the extent of proliferation, of the CD8 T cells they activate. It is now reported here that interaction of primary CD8 T cells with splenic CD8α - DC induced much higher production of IL-3, IFN-γ and granulocyte-macrophage colony-stimulating factor (GM-CSF), as well as IL-2, than did interaction with CD8α+ splenic DC. Furthermore, the CD8α- DC also induced higher levels of IL-2, IL-3 and IL-10 production in primary CD4 T cells, compared with that induced by CD8α+ DC. These quantitative differences did not involve qualitative shifts in the type of cytokine produced. Interleukin-4 production remained low in all the primary T cell cultures and restimulation experiments in secondary cultures did not reveal any bias in the cytokine production profile. When exogenous IL-2 was added to the primary cultures to ensure equal proliferation in response to CD8α - or CD8α+ DC, the higher level of production of IL-3, IFN-γ and GM-CSF induced by CD8α- DC was maintained. Thus, this general control of T cell cytokine production by splenic DC involves factors additional to those that govern activation of T cells into cell cycle. Previous work has established that the dendritic cells (DC) of mouse spleen regulate the IL‐2 production, and hence the extent of proliferation, of the CD8 T cells they activate. It is now reported here that interaction of primary CD8 T cells with splenic CD8α DC induced much higher production of IL‐3, IFN‐γ and granulocyte‐macrophage colony‐stimulating factor (GM‐CSF), as well as IL‐2, than did interaction with CD8α + splenic DC. Furthermore, the CD8α DC also induced higher levels of IL‐2, IL‐3 and IL‐10 production in primary CD4 T cells, compared with that induced by CD8α + DC. These quantitative differences did not involve qualitative shifts in the type of cytokine produced. Interleukin‐4 production remained low in all the primary T cell cultures and restimulation experiments in secondary cultures did not reveal any bias in the cytokine production profile. When exogenous IL‐2 was added to the primary cultures to ensure equal proliferation in response to CD8α or CD8α + DC, the higher level of production of IL‐3, IFN‐γ and GM‐CSF induced by CD8α DC was maintained. Thus, this general control of T cell cytokine production by splenic DC involves factors additional to those that govern activation of T cells into cell cycle. Previous work has established that the dendritic cells (DC) of mouse spleen regulate the IL‐2 production, and hence the extent of proliferation, of the CD8 T cells they activate. It is now reported here that interaction of primary CD8 T cells with splenic CD8α DC induced much higher production of IL‐3, IFN‐γ and granulocyte‐macrophage colony‐stimulating factor (GM‐CSF), as well as IL‐2, than did interaction with CD8α+ splenic DC. Furthermore, the CD8α DC also induced higher levels of IL‐2, IL‐3 and IL‐10 production in primary CD4 T cells, compared with that induced by CD8α+ DC. These quantitative differences did not involve qualitative shifts in the type of cytokine produced. Interleukin‐4 production remained low in all the primary T cell cultures and restimulation experiments in secondary cultures did not reveal any bias in the cytokine production profile. When exogenous IL‐2 was added to the primary cultures to ensure equal proliferation in response to CD8α or CD8α+ DC, the higher level of production of IL‐3, IFN‐γ and GM‐CSF induced by CD8α DC was maintained. Thus, this general control of T cell cytokine production by splenic DC involves factors additional to those that govern activation of T cells into cell cycle. |
Author | Shortman, Ken Hochrein, Hubertus Kelso, Anne Kronin, Vadim |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/10849109$$D View this record in MEDLINE/PubMed |
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Snippet | Previous work has established that the dendritic cells (DC) of mouse spleen regulate the IL‐2 production, and hence the extent of proliferation, of the CD8 T... Previous work has established that the dendritic cells (DC) of mouse spleen regulate the IL-2 production, and hence the extent of proliferation, of the CD8 T... SummaryPrevious work has established that the dendritic cells (DC) of mouse spleen regulate the IL-2 production, and hence the extent of proliferation, of the... |
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SubjectTerms | AIDS/HIV Animals CD4-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - immunology Cell Communication cell‐to‐cell interactions cytokine Cytokines - analysis dendritic cell Dendritic Cells - immunology Dendritic Cells - physiology Female g-Interferon Granulocyte-Macrophage Colony-Stimulating Factor - analysis Interferon-gamma - analysis Interleukin-2 - analysis Interleukin-3 - analysis Lymphocyte Activation Male Mice Mice, Inbred BALB C Mice, Inbred C3H Mice, Inbred C57BL Mice, Inbred CBA Mice, Knockout Mice, Mutant Strains Specific Pathogen-Free Organisms Spleen - immunology T lymphocyte T-Lymphocytes - immunology |
Title | Regulation of T cell cytokine production by dendritic cells |
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