Murine NKT cells produce Th17 cytokine interleukin-22 |
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Authors: | Megumi Goto Kumiko Kadoshima-Yamaoka Kazuhiro Nagahira Takashi Nishimura |
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Affiliation: | a Biomedical Research Laboratories, Asubio Pharma Co., Limited, 1-1-1 Wakayamadai, Shimamoto-cho, Mishima-gun, Osaka 618-8503, Japan b Division of Immunoregulation, Section of Disease Control, Institute for Genetic Medicine, Hokkaido University Sapporo, Japan |
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Abstract: | Natural killer T (NKT) cells are known to produce Th17 cytokine IL-17 in addition to Th1/2 cytokines. In this study, the ability of NKT cells to produce IL-22, another Th17 cytokine, was examined in mice. When murine spleen cells were stimulated with α-galactosyl ceramide, a ligand for NKT cells, not only Th1/2 cytokines (IFN-γ, IL-4) but Th17 cytokines (IL-17, IL-22) were produced. NKT cells isolated from splenocytes released IL-17 and IL-22 following CD3, CD3/IL-2 or CD3/CD28 stimulation, in which CD3/CD28 costimulation was most effective. Production of IL-17 and IL-22 in CD4+ and CD8+ T cells from splenocytes was little, if any, even after CD3/CD28 costimulation. Treatment with IL-6/TGF-β decreased CD3/CD28-stimulated production of IL-22, but not that of IL-17, in NKT cells. These findings show for the first time that NKT cells are a cell source of IL-22, and that expression of two Th17 cytokines might be regulated in NKT cells by different mechanisms. |
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Keywords: | Interleukin-22 (IL-22) NKT cells Cytokine Th17 cells |
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