2011 Fiscal Year Final Research Report
The functional role of thrombin cleaved osteopontin for the pathogenesis of atherosclerosis
Project/Area Number |
22790382
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Experimental pathology
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Research Institution | Ehime University |
Principal Investigator |
KURATA Mie 愛媛大学, 大学院・医学系研究科, 講師 (80423440)
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Project Period (FY) |
2010 – 2011
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Keywords | 炎症 / 粥状動脈硬化 / オステオポンチン / トロンビン切断型オステオポンチン |
Research Abstract |
Osteopontin(OPN) which produced in atherosclerotic lesions is cleaved by activated thrombin. We clarified that prevalence of trOPN around intra-plaque vessels which is characterized CD34, recognized as one of the stem cell markers, positive luminal structures. Furthermore, we confirmed that after the mechanical damage of an unstable atherosclerotic plaque increased plasma levels of trOPN. In vitro study, GST-fused recombinant trOPN induced various inflammatory cytokines stronger than fOPN, from mouse resident peritoneal macrophages in a dose dependent manner. These findings suggested that trOPN has a potential not only to be a novel biomarker that reflects the atherothrombotic status in ischemic stroke, but also to be a therapeutic target to suppress the inflammation.
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[Journal Article] Osteopontin deficiency protects against aldosterone-induced inflammation, oxidative stress, and interstitial fibrosis in the kidney2011
Author(s)
Irita J, Okura T, Jotoku M, Nagao T, Enomoto D, Kurata M, Desilva VR, Miyoshi K, Matsui Y, Uede T, Denhardt DT, Rittiling SR, Higaki J
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Journal Title
American Journal of Physiology. Renal Physiology
Volume: 301
Pages: F833-F844
Peer Reviewed
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