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Hematopoietic cell-derived IL-15 supports NK cell development in scattered and clustered localization within the bone marrow.
Abe, Shinya; Asahi, Takuma; Hara, Takahiro; Cui, Guangwei; Shimba, Akihiro; Tani-Ichi, Shizue; Yamada, Kohei; Miyazaki, Kazuko; Miyachi, Hitoshi; Kitano, Satsuki; Nakamura, Naotoshi; Kikuta, Junichi; Vandenbon, Alexis; Miyazaki, Masaki; Yamada, Ryo; Ohteki, Toshiaki; Ishii, Masaru; Sexl, Veronika; Nagasawa, Takashi; Ikuta, Koichi.
Affiliation
  • Abe S; Laboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan; Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan.
  • Asahi T; Laboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan; Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan.
  • Hara T; Laboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
  • Cui G; Laboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
  • Shimba A; Laboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan; Department of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
  • Tani-Ichi S; Laboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan; Department of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
  • Yamada K; Laboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan; Graduate School of Biostudies, Kyoto University, Kyoto 606-8501, Japan.
  • Miyazaki K; Laboratory of Immunology, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
  • Miyachi H; Reproductive Engineering Team, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
  • Kitano S; Reproductive Engineering Team, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
  • Nakamura N; Interdisciplinary Biology Laboratory (iBLab), Division of Natural Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan.
  • Kikuta J; Department of Immunology and Cell Biology, Graduate School of Medicine and Frontier Biosciences, WPI Immunology Frontier Research Center, Osaka University, Suita 565-0871, Japan.
  • Vandenbon A; Laboratory of Tissue Homeostasis, Department of Biosystems Science, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
  • Miyazaki M; Laboratory of Immunology, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
  • Yamada R; Statistical Genetics, Center for Genomic Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
  • Ohteki T; Department of Biodefense Research, Medical Research Institute, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.
  • Ishii M; Department of Immunology and Cell Biology, Graduate School of Medicine and Frontier Biosciences, WPI Immunology Frontier Research Center, Osaka University, Suita 565-0871, Japan.
  • Sexl V; Institute of Pharmacology and Toxicology, Department for Biomedical Sciences, University of Veterinary Medicine Vienna, 1210 Vienna, Austria.
  • Nagasawa T; Laboratory of Stem Cell Biology and Developmental Immunology, Graduate School of Frontier Biosciences and Graduate School of Medicine, WPI Immunology Frontier Research Center, Osaka University, Suita 565-0871, Japan.
  • Ikuta K; Laboratory of Immune Regulation, Department of Virus Research, Institute for Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan. Electronic address: ikuta.koichi.6c@kyoto-u.ac.jp.
Cell Rep ; 42(9): 113127, 2023 09 26.
Article in En | MEDLINE | ID: mdl-37729919
ABSTRACT
Natural killer (NK) cells are innate immune cells critical for protective immune responses against infection and cancer. Although NK cells differentiate in the bone marrow (BM) in an interleukin-15 (IL-15)-dependent manner, the cellular source of IL-15 remains elusive. Using NK cell reporter mice, we show that NK cells are localized in the BM in scattered and clustered manners. NK cell clusters overlap with monocyte and dendritic cell accumulations, whereas scattered NK cells require CXCR4 signaling. Using cell-specific IL-15-deficient mice, we show that hematopoietic cells, but not stromal cells, support NK cell development in the BM through IL-15. In particular, IL-15 produced by monocytes and dendritic cells appears to contribute to NK cell development. These results demonstrate that hematopoietic cells are the IL-15 niche for NK cell development in the BM and that BM NK cells are present in scattered and clustered compartments by different mechanisms, suggesting their distinct functions in the immune response.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Marrow / Interleukin-15 Limits: Animals Language: En Journal: Cell Rep Year: 2023 Type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Marrow / Interleukin-15 Limits: Animals Language: En Journal: Cell Rep Year: 2023 Type: Article Affiliation country: Japan