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Key Molecules involved in the Early Phase of Anterior Uveitis

Research Project

Project/Area Number 09671793
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Ophthalmology
Research InstitutionKYOTO UNIVERSITY

Principal Investigator

MANDAI Michiko  Kyoto University Graduate School of Medicine, Assistant Professor, 医学研究科, 助手 (80263086)

Co-Investigator(Kenkyū-buntansha) TAKAGI Hitoshi  Kyoto University Graduate School of Medicine, Assistant Professor, 医学研究科, 助手 (70283596)
KASHII Satoshi  Kyoto University Graduate School of Medicine, Lecturer, 医学研究科, 講師 (50194717)
TANIHARA Hidenobu  Kyoto University Graduate School of Medicine, Lecturer, 医学研究科, 講師 (60217148)
Project Period (FY) 1997 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 1998: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 1997: ¥2,000,000 (Direct Cost: ¥2,000,000)
KeywordsLPS / cellular infiltration / endotoxin-induced uveitis / E-selectin / P-selectin / estrpgen / gene expression / vaxcular endothelium / エンドトキシンぶどう膜炎 / タモキシフェン / モノクローナル抗体
Research Abstract

Endotoxin-induced uveitis (EIU) is an animal model of acute ocular inflammation caused by the injection of lipopolysaccharide (LPS). Selectins area group of molecules involved in rolling of leukocytes, the initial step of cellular infiltration. Among them, P-selectin is stored in the vascular endothelial cell body and translocated to the surface upon stimulation, whereas E-selectin is regulated at the transcriptional level of the gene. In EIU, we found that P-selectin appeared immunohistochemically on the endothelial surface of the vessels of iris-ciliary body after 15 minutes of LPS treatment, followed by its second expression at 3-5 hours after LPS injection, and that E-selectin appeared 7-24 hours after LPS treatment. Each of the neutralizing antibodies against P- and E-selectin similarly reduced the cellular infiltration in EIU, but anti P-selectin antibody given at 6 hours after LPS treatment did not significantly inhibit the cellular infiltration whereas anti E-selectin antibody … More given at any time after LPS treatment significantly reduced cellular infiltration thereafter. Semi-quantitative PCR revealed that E-selectin gene expression reached a peak at 6 hours after LPS treatment both in the iris-ciliary body and retina, and it returned to the basal level at the time of maximum uveitis. Simultaneous injection of anti P-and E-selectin antibodies almost abrogated cellular infiltration. These suggested that P-selectin is involved in the initiation of cellular infiltration whereas E-selectin contributes to retain cellular infiltration ; the inhibition of the former may contribute to the prevention of inflammation and the latter, to the early resolution of the inflammation. Next we focused on the fact that anterior uveitis associated with massive cellular infiltration is more often observed in men than in women, and we are studying the role of estrogen against cellular infiltration in EIU.Estrogen receptor-like immunoreactivity was found on the vascular endothelium of iris-ciliary body, and the degree of cellular infiltration was in the order of male>ovariectomized female>female rats. Intraperitoneal injection of estradiol significantly reduced cellular infiltration and the E-selectin gene expression, indicating that estrogen protects against cellular infiltration by modulation the selectin expression. Less

Report

(3 results)
  • 1998 Annual Research Report   Final Research Report Summary
  • 1997 Annual Research Report
  • Research Products

    (6 results)

All Other

All Publications (6 results)

  • [Publications] Kiyoshi, Suzuma: "Role of P-selectin in endotoxin-induced uveitis" Investigative Ophthalmology and Visual Science. 38. 1610-1618 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Izumi, Suzuma: "Contibution of E-selectin to cellular infiltration during endotoxin-induced uveitis" Investigative Ophthalmology and Visual Science. 39. 1620-1630 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Suzuma K,Mandai M,Kogishi J,Honda Y and Yoshimura N: "Role of P-selectin in endotoxin-induced uveitis." Invest Ophthal Vis. 38. 1610-1618 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Suzuma I,Mandai M,Suzuma K,Ishida K,Tojo S and Honda Y: "Contribution of E-selectin to cellular infiltration during endotoxin-induced uveitis." Invest Ophthalmol Vis Sci. 39. 1620-1630 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Izumi Suzuma: "Contribution of E-selectin to cellular infiltration during endotoxin-induced uveitis" Investigative Ophthalmology and Visual Science. 39. 1620-1630 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Kiyoshi Suzuma: "Role of P-selectin in Endotoxin-induced Uveitis" Invest Ophthalmol Vis Sci.38. 1610-1618 (1997)

    • Related Report
      1997 Annual Research Report

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Published: 1997-04-01   Modified: 2016-04-21  

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