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2019 Fiscal Year Final Research Report

Role of inflamasome in corneal inflammation

Research Project

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Project/Area Number 17K11468
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Ophthalmology
Research InstitutionNihon University

Principal Investigator

SAKIMOTO Tohru  日本大学, 医学部, 准教授 (20465272)

Co-Investigator(Kenkyū-buntansha) 山上 聡  日本大学, 医学部, 教授 (10220245)
Project Period (FY) 2017-04-01 – 2020-03-31
Keywords角膜 / 炎症 / インフラマソーム
Outline of Final Research Achievements

We evaluated the role of NLR family pyrin domain containing 3 (NLRP3) inflammasome in sterile corneal inflammation caused by lipopolysaccharide (LPS) or alkali burns in C57BL6 mice or NLRP3 KO (Nlrp3-/-) mice. Various molecules related to the NLRP3 inflammasome were upregulated in C57BL6 mice after both alkali burn injury and LPS treatment. After alkali burn injury, the corneal opacity grade was significantly reduced in Nlrp3-/- mice compared with C57BL6 mice. In Nlrp3-/- mice, Gr-1 immunoreactivity and MMP-9 mRNA expression in the corneal stroma were significantly reduced by both LPS treatment and alkali burn injury. Quantitative PCR and immunohistochemistry revealed that IL-1β and MMP-9 expression in the corneal stroma were down-regulated in Nlrp3-/- mice with both alkali burn injury and LPS treatment. These findings suggest that the NLRP3 inflammasome has a proinflammatory effect in the cornea by recruiting neutrophils to sites of inflammation.

Free Research Field

角膜

Academic Significance and Societal Importance of the Research Achievements

各領域の様々な慢性疾患や炎症性疾患での関与を指摘されているNLRP3インフラマソームが、無菌性角膜炎症において炎症促進に関与していることを初めて明らかにした。また、角膜におけるNLRP3は好中球依存性にIL-1β・MMP-9発現を誘導し、炎症促進に関与することを示した。これらのことから、角膜における無菌性炎症である周辺部角膜潰瘍などの非感染性角膜潰瘍の病態にNLRP3インフラマソームが関与する可能性を示した。

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Published: 2021-02-19  

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