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2016 Fiscal Year Final Research Report

The establishment of the novel murine model of the antiphospholipid syndrome

Research Project

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Project/Area Number 26293230
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypePartial Multi-year Fund
Section一般
Research Field Collagenous pathology/Allergology
Research InstitutionHokkaido University

Principal Investigator

Tatsuya Atsumi  北海道大学, 医学(系)研究科(研究院), 教授 (20301905)

Co-Investigator(Kenkyū-buntansha) 奥 健志  北海道大学, 大学病院, 助教 (70544295)
Project Period (FY) 2014-04-01 – 2017-03-31
Keywords内科 / 免疫学 / 脂質 / 生体分子
Outline of Final Research Achievements

We have strived to develop novel APS animal model using arteriosclerotic mouse model with additional monoclonal aPL administration, however, failed to develop the spontaneous thrombosis.
Recently, we have clarified that abnormal acceleration of the complement activation contributes to APS pathogenesis and the autoantibody against first component of the classical pathway (C1q), highly produced in the patients' sera, initiates the activation. Additionally, in APS, primary abnormality of the vascular endothelial cells,especially dysfunction of endothelial NOS(eNOS) secretion is reported.These factors facilitates aPL to bind the cell surfaces of vascular endothelial cells via inducing anionic phospholipids expressions on cell membranes. And these processes result to the up-regulation of pro-thrombotic states of the cells.We are now planning to establish APS model mouse by using eNOS KO mouse with the pathogenic autoantibodies (aPL, anti-C1q antibody) which seems promising

Free Research Field

膠原病内科学

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Published: 2018-03-22  

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