Role of AMPK in HDL-induced antiarterogenic effects in endothelial cells
Project/Area Number |
23591331
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Metabolomics
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Research Institution | Gunma University |
Principal Investigator |
KIMURA Takao 群馬大学, 医学(系)研究科(研究院), 講師 (90396656)
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Project Period (FY) |
2011 – 2013
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Project Status |
Completed (Fiscal Year 2013)
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Budget Amount *help |
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2013: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2012: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2011: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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Keywords | 脂質代謝異常 / 動脈硬化 / HDL / 血管内皮細胞 / S1P / スカベンジャー受容体 / スフィンゴシン1-リン酸 / AMPK |
Research Abstract |
High density lipoprotein (HDL) stimulated AMP kinase (AMPK) in human umbilical vein endothelial cells (HUVECs). HDL activated AMPK through independent two pathways. HDL-induced AMPK activation was mediated by sphingosine-1 phosphate (S1P)/S1P receptor pathway and scavenger receptor (SR-BI)/PDZK-1. S1P/S1P receptor pathway was mediated by calmodulin. SR-BI/PDZK-1 pathway was mediated by calmodulin and LKB1 in HUVECs. Simvastatin, fenofibrate, metrformin and AICAR enhanced protein expression of SR-BI and endothelial nitric oxide synthase (eNOS) in HUVECs. Simultaneous pretreatment of simvastatin and fenofibrate enhanced HDL-induced AMPK/Akt activation in HUVECs.
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Report
(4 results)
Research Products
(14 results)
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[Presentation] Tuberculosis screening by a T cell interferon-release assay in students of medical school and international students in Gunma University2012
Author(s)
R. Watanabe, T. Kimur a, Y. Tokue, T. Ogiwara, M. Nara, Y. Kobayashi, T. Inoue, H. Sumino, T. Morimura, O. Araki, K. Tsunekawa, T. Aoki, T. Obuchi, Y. Yomoda, K. Ohshima, M. Murakami
Organizer
The12^<th> meeting of the Asian Society of Clinical Pathology and Laboratory Medicine
Place of Presentation
京都国際会館
Year and Date
2012-12-01
Related Report
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