イヌの骨髄由来樹状細胞の効率的な誘導

  • ISOTANI Mayu
    Department of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University
  • KATSUMA Kensuke
    Department of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University
  • TAMURA Kyoichi
    Department of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University
  • YAMADA Misato
    Department of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University
  • YAGIHARA Hiroko
    Department of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University
  • AZAKAMI Daigo
    Department of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University
  • ONO Kenichiro
    Department of Veterinary Clinical Pathobiology, Graduate School of Agricultural and Life Sciences, The University of Tokyo
  • WASHIZU Tsukimi
    Department of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University
  • BONKOBARA Makoto
    Department of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University

書誌事項

タイトル別名
  • Efficient Generation of Canine Bone Marrow-Derived Dendritic Cells

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Because of their unsurpassed potency in presenting antigens to naive T cells, dendritic cells are considered to be an important candidate in the development of immunotherapeutic strategies. Despite the high potential of dendritic cell-based immunotherapy, as a so-called dendritic cell vaccination, few clinical approaches using dendritic cell vaccination have been performed in the dog because of very limited information regarding the generation of canine dendritic cells and their functional properties. We therefore established a protocol for the efficient generation of dendritic cells from canine bone marrow cells using recombinant feline granulocyte-macrophage colony-stimulating factor and canine interleukin-4. Dendritic cells were generated efficiently: a yield of 1-9 × 106 cells per approximately 0.5 ml of canine bone marrow aspiration was achieved. These dendritic cells showed features shared with mouse and human dendritic cells: dendrite morphology, expression of surface markers MHC class II and CD11c, and up-regulation of molecules related to antigen presentation (MHC class II, B7-1, and B7-2) by activation with lipopolysaccharide. Moreover, the dendritic cells demonstrated phagocytic activity, processing activity of pinocytosed proteins, and activation of allogeneic T cells far more potent than that by macrophages. Our findings suggest that the bone marrow-derived dendritic cells are functional for the capturing and processing of antigens and the initiation of T cell responses.<br>

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