2013 Fiscal Year Final Research Report
Genetic analysis of molecular mechanisms of foam cell formation in atherosclerosis
Project/Area Number |
23591339
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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 | Jichi Medical University |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
ISHIBASHI Shun 自治医科大学, 医学部, 教授 (90212919)
YAGYU Hiroaki 自治医科大学, 医学部, 非常勤講師 (60348018)
|
Project Period (FY) |
2011 – 2013
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Keywords | マクロファージ / コレステロールエステル / 泡沫化 / 粥状動脈硬化症 |
Research Abstract |
NCEH1 plays a principal role for cholesteryl ester hydrolase at optimal neutral pH in macrophages. Gene-knockout studies revealed that NCEH1 would have a deep relationship with foam cell formation and atherosclerotic development. In addition, it is suggested by experiments using the enzymatic inhibitor that NCEH1 might be a main enzyme in human macrophages and immunohistochemical analyses demonstrate that NCEH1 exists in the aortic area stained by anti-CD68 antibody. Furthermore oxysterols could augment the induction of apoptosis in foam cells lacking NCEH1 and advance the severity of atherosclerotic lesions. NCEH1 is a key molecule to understand the pathogenesis of atherosclerosis and lead to clinical applications including its diagnosis and treatment.
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Research Products
(6 results)
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[Journal Article] Apolipoprotein C-II deficiency with no rare variant in the APOC2 gene2013
Author(s)
Takase S, Osuga J, Fujita H, Hara K, Sekiya M, Igarashi M, Takanashi M, Takeuchi Y, Izumida Y, Ohta K, Kumagai M, Nishi M, Kubota M, Masuda Y, Taira Y, Okazaki S, Iizuka Y, Yahagi N, Ohashi K, Yoshida H, Yanai H, Tada N, Gotoda T, Ishibashi S, Kadowaki T, Okazaki H
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Journal Title
J Atheroscler Thromb
Volume: 20(5)(Epub 2013 Mar 7)
Pages: 481-93
URL
Peer Reviewed
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[Journal Article] Liver-specific deletion of 3-hydroxy-3-methylglutaryl coenzyme A reductase causes hepatic steatosis and death2012
Author(s)
Nagashima S, Yagyu H, Ohashi K, Tazoe F, Takahashi M, Ohshiro T, Bayasgalan T, Okada K, Sekiya M, Osuga J, Ishibashi S
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Journal Title
Arterioscler Thromb Vasc Biol
Volume: 32(8)(Epub 2012 Jun 14)
Pages: 1824-31
DOI
Peer Reviewed
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[Journal Article] Molecular analysis of a novel LCAT mutation (Gly179→Arg) found in a patient with complete LCAT deficiency2011
Author(s)
Wang XL, Osuga J, Tazoe F, Okada K, Nagashima S, Takahashi M, Ohshiro T, Bayasgalan T, Yagyu H, Okada K, Ishibashi S
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Journal Title
J Atheroscler Thromb
Volume: 18(8)(Epub 2011 May 20)
Pages: 713-9
URL
Peer Reviewed
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