Abstract
Plasmacytoid dendritic cells (pDC) are the producers of type I IFNs in response to TLR9 ligands. However, we have found that when bone marrow is depleted of pDC, the IFN-α produced in response to TLR9 ligands is not fully removed. We assign the source of this non-pDC IFN-α as a newly described DC type. It displays the high IFN-α producing activity of pDC but to a more limited range of viruses. Unlike pDC, the novel DC display high T cell stimulation capacity. Moreover, unlike mouse pDC, they are matured with GM-CSF and are less prone to apoptosis upon activation stimuli, including viruses. We propose that these DC constitute a novel bone marrow inflammatory DC type, ideally geared to linking innate and adaptive immune responses in bone marrow via their potent IFN-α production and high T cell stimulatory capacity.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adaptive Immunity
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Animals
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Apoptosis
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Bone Marrow Cells / cytology
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Bone Marrow Cells / immunology*
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Dendritic Cells / cytology
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Dendritic Cells / immunology*
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Female
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Granulocyte-Macrophage Colony-Stimulating Factor / immunology
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Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
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Humans
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Immunity, Innate
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Interferon-alpha / biosynthesis
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Interferon-alpha / immunology*
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Lipopolysaccharides / pharmacology
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Lymphocyte Activation
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Male
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Mice
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Mice, Inbred C57BL
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Poly I-C / pharmacology
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Signal Transduction
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T-Lymphocytes / cytology
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T-Lymphocytes / immunology*
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Toll-Like Receptor 9 / genetics
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Toll-Like Receptor 9 / immunology
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Vaccinia virus / genetics
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Vaccinia virus / immunology
Substances
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Interferon-alpha
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Lipopolysaccharides
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Tlr9 protein, mouse
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Toll-Like Receptor 9
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Granulocyte-Macrophage Colony-Stimulating Factor
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Poly I-C