2013 Fiscal Year Final Research Report
Prevention of Left Ventricular Remodeling after Acute Myocardial Infarction in Interleukin-17 Deficient Mice
Project/Area Number |
24790788
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Circulatory organs internal medicine
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Research Institution | Kurume University |
Principal Investigator |
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Project Period (FY) |
2012-04-01 – 2014-03-31
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Keywords | 生体分子 / シグナル伝達 |
Research Abstract |
Post-infarct mortality was prevented in interleukin-17 knockout mice (IL17-KO) compared with wild-type mice. Left ventricular dysfunction, increase in LV weight to body weight ratio, and myocardial fibrosis 28 days after myocardial infarction were significantly attenuated in IL17-KO mice compared with wild-type mice. To investigate the mechanism for left ventricular remodeling inhibition in IL17-KO mice, we conducted microarray analysis. Microarray analysis revealed that the expressions of extracellular matrix related genes were lower in IL17-KO mice than those in wild-type mice. These results suggest that IL17 may play a pathogenic role in the development of left ventricular remodeling after myocardial infarction, possibly through the regulation of extracellular matrix genes expression.
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[Journal Article] Screening for Fabry disease in patients with left ventricular hypertrophy2013
Author(s)
Mawatari K, Yasukawa H, Oba T, Nagata T, Togawa T, Tsukimura T, Kyogoku S, Ohshima H, Minami T, Sakubaba H, Imaizumi T
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Journal Title
Int J Cardiol
Volume: 167(3)
Pages: 1059-61
Peer Reviewed
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[Journal Article] Cardiac-specific deletion of SOCS-3 prevents development of left ventricular remodeling after acute myocardial infarction2012
Author(s)
Oba T, Yasukawa H, Hoshijima M, Sasaki K, Futamata N, Fukui D, Mawatari K, Nagata T, Kyogoku S, Ohshima H, Minami T, Nakamura K, Kang D, Yajima T, Knowlton KU, Imaizumi T
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Journal Title
J Am Coll Cardiol
Volume: 59(9)
Pages: 838-852
Peer Reviewed