• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to project page

1998 Fiscal Year Final Research Report Summary

Critical role of IL-18 in endotoxin-induced liver injury.

Research Project

Project/Area Number 09670499
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field 内科学一般
Research InstitutionHyogo College of Medicine

Principal Investigator

TSUTSUI Hiroko  Hyogo College of Medicine, Lecturer, 医学部, 講師 (40236914)

Co-Investigator(Kenkyū-buntansha) AKIRA Shizuo  Hyogo College of Medicine, Professor, 医学部, 教授 (50192919)
NAKANISHI Kenji  Hyogo College of Medicine, Professor, 医学部, 教授 (60172350)
OKAMURA Haruki  Hyogo College of Medicine, Associated Professor, 医学部, 助教授 (60111043)
Project Period (FY) 1997 – 1998
Keywordsinterleukin 18 / endotoxin / liver injury / macrophages / NK cells / caspase-1 / receptor for IL-18 / knockout mice
Research Abstract

IL-18 is a pleiotropic cytokine. IL-18 induces IFN-gamma in lymphocytes, upregulates functional Fas ligand expression of lymphocytes and also augments NK activity. Initially, IL-18 was discovered in the injured liver of the mice that had been sequentially administered with heat-killed Propionibacterium acnes (P.acnes) and endotoxin (LPS). IL- 18 is secreted by LPS-activated P.acnes-elicited Kupffer cells. IL-18 is produced by these cells as biologically inactive precursor form (prolL-18), and prolL-18 is cleaved into mature IL-18 by intracellular cysteine proteinase, caspase-l. In this study, we investigated the precise mechanism how IL-18 is involved in endotoxin-induced liver injury and found the followings. First, IL-18-deficient mice are resistant to endotoxin-induced liver injury, but highly sensitive to endotoxin-induced lethality, suggesting that IL-18 might be critical to endotoxin-induced liver injury. In addition, T cells in IL-18-deficient mice are impaired in the differentiation into Th1, a prototpe to inflammation, and NK activity of the mice also is defective, indicating that IL-18 is essential for functional development of immune system. Second, receptor for IL-18 is constitutively expressed on NK cells, whereas its expression on T cells is induced after stimulation with IL-12. MyD 88, an adapter molecule for the activation of receptor for IL-1 is critical for the signal transduction of IL-18. Lymphocytes from MyD88-deficient mice do not respond to IL-18 as well as IL-1. Third, caspase-1 deficient mice are resistant to the endotoxin-induced liver injury without showing early elevation of serum IL- 18 level, suggesting caspase- 1 is critical for IL- 18 secretion after stimulation with LPS.These results suggested that IL-18 might be an essential factor for endotoxin-induced liver injury.

  • Research Products

    (16 results)

All Other

All Publications (16 results)

  • [Publications] Hyodo, Y., et al: "IL-18 up-regulates perforin-mediated NK activity without increasing perforin messenger RNA expression by binding to constitutively expressed IL-18R." J.Immunol.162. 1662-1669 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Adachi, O., et al: "Tageted disruption of the MyD88 gene results in loss IL-1-and IL-18-mediated function." Immunity. 9. 143-150 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Takeda, K.,et al: "Defective NK cell activity and Th1 response in IL-18-deficient mice." Immunity. 8. 383-390 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Gu, Y., et al: "Activation of Interferon-γ inducing factor mediated by Interferon-1β converting enzyme." Science. 275. 206-209 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Tsutsui, H., et al: "IL-18 accounts for both TNF-α-and Fas Ligand-mediated hepatotoxic pathways in endotoxin-induced liver injury in mice." J.Immunol.159. 3961-3967 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Matsui, K., et al: "Propionibacterium acnes treatment diminishes CD4^+NK1.1^+T cells but induces Type 1 T cells in the liver by induction of IL-12 and IL-18." J.Immunol.159. 97-106 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 筒井ひろ子, 他: "臨床免疫, 30(4)" Caspase-1はIL-18前駆体を切断する, 4 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 筒井ひろ子, 他: "臨床免疫、30(12)," エンドトキシン肝障害とinterleukin 18, 5 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Tsutsui, H., et al: "IL-18 accounts for both TNF-alpha-and Fas Ligand-mediated hepatotoxic pathways in endotoxin-induced liver injury in mice." J.Immunol.159. 3961-3967 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Matsui, K., et al: "Propionibacterium acnes treatment diminishes CD4^+NK1.1^+ T cells but induces Type 1 T cells in the liver by induction of IL-12 and IL-18." J.Immunol.159. 97-106 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Adachi, O., et al: "Tageted disruption of the MyD88 gene results in loss of IL-1-and IL-18-mediated function." Immunity. 9. 143-150 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takeda, K., et al: "Defective NK cell activity and Th1 response in IL-18-deficient mice." Immunity. 8. 383-390 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Sakao, Y., et al: "IL-18-deficient mice are resistant to endotoxin-induced liver injury but highly susceptible to endotoxin shock." Int.Immunol.(in press). (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Hyodo, Y., et al: "IL-18 up-regulates perforin-mediated NK activity without increasing perforin messenger RNA expression by binding to constitutively expressed IL-18R." J.Immunol.162. 1662-1669 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Okamura, H., et al: "Interleukin-18 (IL-18) : a novel cytokine that auguments both innate and acquired immunity." Adv.Immunol.70. 281-312 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Okamura, H., et al: "Regulation of interferon-gamma (IFN-gamma) production by IL-12 and IL-18." Current Opinion in Immnology.10. 259-264 (1998)

    • Description
      「研究成果報告書概要(欧文)」より

URL: 

Published: 1999-12-08  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi