mortality/aging
• in mice with diphtheria toxin induced plasmacytoid dendritic cell ablation survival is improved following lethal shock trigger by CpG-A in D-galactosamine (D-GalN)-sensitized mice
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• plasmacytoid dendritic cell ablated mutant mice are resistant to infection with Listeria monocytogenes expressing OVA
• plasmacytoid dendritic cell ablated mutant mice show increased numbers of CD11c+B22- dendritic cells and lower bacterial burden 3 days after infection with Listeria monocytogenes expressing OVA
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immune system
• by 2 days after treatment with diphtheria toxin plasmacytoid dendritic cells are almost completely ablated but numbers rebound by 10 days after treatment
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• in mutant mice
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• markedly enhanced in plasmacytoid dendritic cell ablated mutant mice
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• slightly higher frequency and number of thymic CD4+Foxp3+ regulatory T cells in mutant mice and in plasmacytoid dendritic cell ablated mutant mice compared to wild-type controls
• decrease in the number of CD4+Foxp3+ regulatory T cells in the lamina propria of the small intestine in plasmacytoid dendritic cell ablated mice compared to wild-type controls
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• increase in serum cytokines after injection with CpG-A plus D-GalN
• decrease in serum cytokines in plasmacytoid dendritic cell ablated mice following treatment with CpG-A compared to wild-type controls
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• in plasmacytoid dendritic cell ablated mice following treatment with CpG-A or infection with HSV-1 compared to wild-type controls
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• CpG-A induced and HSV-1 induced IFNA production is enhanced compared to wild-type controls
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• in plasmacytoid dendritic cell ablated mice following treatment with CpG-A or infection with HSV-1 compared to wild-type controls
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• CpG-A induced and HSV-1 IL12B production is enhanced compared to wild-type controls
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• reduced capacity to present OVA protein and peptide for priming of Tg(TcraTcrb)425Cbn CD4+ T cells in culture
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• reduced cell surface levels of SIGLECH and B220 and increased levels of CD11C and BST2
• increased production of IFNA and IL12B
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• in mice with diphtheria toxin induced plasmacytoid dendritic cell ablation survival is improved following lethal shock trigger by CpG-A in D-galactosamine (D-GalN)-sensitized mice
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• plasmacytoid dendritic cell ablated mutant mice are resistant to infection with Listeria monocytogenes expressing OVA
• plasmacytoid dendritic cell ablated mutant mice show increased numbers of CD11c+B22- dendritic cells and lower bacterial burden 3 days after infection with Listeria monocytogenes expressing OVA
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homeostasis/metabolism
• increase in serum cytokines after injection with CpG-A plus D-GalN
• decrease in serum cytokines in plasmacytoid dendritic cell ablated mice following treatment with CpG-A compared to wild-type controls
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• in plasmacytoid dendritic cell ablated mice following treatment with CpG-A or infection with HSV-1 compared to wild-type controls
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• CpG-A induced and HSV-1 induced IFNA production is enhanced compared to wild-type controls
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• in plasmacytoid dendritic cell ablated mice following treatment with CpG-A or infection with HSV-1 compared to wild-type controls
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• CpG-A induced and HSV-1 IL12B production is enhanced compared to wild-type controls
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hematopoietic system
• by 2 days after treatment with diphtheria toxin plasmacytoid dendritic cells are almost completely ablated but numbers rebound by 10 days after treatment
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• in mutant mice
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• markedly enhanced in plasmacytoid dendritic cell ablated mutant mice
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• slightly higher frequency and number of thymic CD4+Foxp3+ regulatory T cells in mutant mice and in plasmacytoid dendritic cell ablated mutant mice compared to wild-type controls
• decrease in the number of CD4+Foxp3+ regulatory T cells in the lamina propria of the small intestine in plasmacytoid dendritic cell ablated mice compared to wild-type controls
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