Interleukin 15–dependent crosstalk between conventional and plasmacytoid dendritic cells is essential for CpG-induced immune activation

被引:0
|
作者
Seiichi Kuwajima
Taku Sato
Kazuto Ishida
Hiroyuki Tada
Hiroyuki Tezuka
Toshiaki Ohteki
机构
[1] Akita University School of Medicine,Department of Immunology
来源
Nature Immunology | 2006年 / 7卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
The function of interleukin 15 (IL-15) in unmethylated CpG oligodeoxynucleotide (CpG)–induced immune responses remains unknown. Here, in response to CpG, both wild-type and natural killer cell–depleted mice produced IL-12 and became resistant to a lethal dose of Listeria monocytogenes. In contrast, CpG-treated IL-15-deficient mice produced little IL-12 and succumbed to L. monocytogenes. CpG-stimulated conventional dendritic cells (cDCs) were the main producers of both IL-15 and IL-12, but cDCs did not produce IL-12 in the absence of plasmacytoid DCs (pDCs). The cDC-derived IL-15 induced CD40 expression by cDCs. Interaction between CD40 on cDCs and CD40 ligand on pDCs led to IL-12 production by cDCs. Thus, IL-15-dependent crosstalk between cDCs and pDCs is essential for CpG-induced immune activation.
引用
收藏
页码:740 / 746
页数:6
相关论文
共 20 条
  • [1] Interleukin 15-dependent crosstalk between conventional and plasmacytoid dendritic cells is essential for CpG-induced immune activation
    Kuwajima, Seiichi
    Sato, Taku
    Ishida, Kazuto
    Tada, Hiroyuki
    Tezuka, Hiroyuki
    Ohteki, Toshiaki
    NATURE IMMUNOLOGY, 2006, 7 (07) : 740 - 746
  • [2] CpG-Induced IFN-α Production of Plasmacytoid Dendritic Cells: Time and Dosage Dependence and the Effect of Structural Modifications to the CpG Backbone
    Jeske, Sabrina
    Pries, Ralph
    Wollenberg, Barbara
    NUCLEIC ACID THERAPEUTICS, 2013, 23 (02) : 118 - 124
  • [3] Innate Immune Cell Production Of Interleukin-12 Drives CpG-Induced Macrophage Activation Syndrome
    Weaver, Lehn K.
    Behrens, Edward M.
    ARTHRITIS AND RHEUMATISM, 2013, 65 : S494 - S494
  • [4] Vinpocetine Inhibited the CpG Oligodeoxynucleotide-induced Immune Response in Plasmacytoid Dendritic Cells
    Feng, Xungang
    Wang, Yuzhong
    Hao, Yanlei
    Ma, Qun
    Dai, Jun
    Liang, Zhibo
    Liu, Yantao
    Li, Xiangyuan
    Song, Yan
    Si, Chuanping
    IMMUNOLOGICAL INVESTIGATIONS, 2017, 46 (03) : 263 - 273
  • [5] Two distinct activation states of plasmacytoid dendritic cells induced by influenza virus and CpG 1826 oligonucleotide
    Iparraguirre, Amaya
    Tobias, John W.
    Hensley, Scott E.
    Masek, Katherine S.
    Cavanagh, Lois L.
    Rendl, Michael
    Hunter, Christopher A.
    Ertl, Hildegund C.
    von Andrian, Ulrich. H.
    Weninger, Wolfgang
    JOURNAL OF LEUKOCYTE BIOLOGY, 2008, 83 (03) : 610 - 620
  • [6] IL-15-dependent immune crosstalk between natural killer cells and dendritic cells in HIV-1 elite controllers
    Hartana, Ciputra Adijaya
    Lancien, Melanie
    Gao, Ce
    Rassadkina, Yelizaveta
    Lichterfeld, Mathias
    Yu, Xu G.
    CELL REPORTS, 2023, 42 (12):
  • [7] Interleukin-2 Controls flt3L-dependent Development and Phenotype of Conventional and Plasmacytoid Dendritic Cells
    Lau-Kilby, Annie
    Kretz, Cosima
    O'Shea, John
    Trinchieri, Giorgio
    Tarbell, Kristin
    JOURNAL OF IMMUNOLOGY, 2010, 184
  • [8] p38 MAPK is critical for nuclear translocation of IRF-7 during CpG-induced type I IFN expression in human plasmacytoid dendritic cells
    Wang, Qi
    Reszka-Blanco, Natalia
    Cheng, Liang
    Li, Guangming
    Zhang, Liguo
    Su, Lishan
    JOURNAL OF IMMUNOLOGY, 2018, 200 (01):
  • [9] Plasmacytoid and conventional dendritic cells mediate rapid cytokine-dependent activation of NK cells to herpes simplex virus type 1
    Barr, DP
    Reading, PC
    Wojtasiak, M
    Whitney, PG
    Belz, GT
    Brooks, AG
    TISSUE ANTIGENS, 2005, 66 (05): : 354 - 354
  • [10] Spleen Tyrosine Kinase (Syk)-dependent Calcium Signals Mediate Efficient CpG-induced Exocytosis of Tumor Necrosis Factor α (TNF α) in Innate Immune Cells
    Rao, Sheila
    Liu, Xiaohong
    Freedman, Bruce D.
    Behrens, Edward M.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (18) : 12448 - 12458