Disease analysis of Hypertrophic cardiomyopathy using patient specific induced pluripotent stem cells
Project/Area Number |
22790726
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Circulatory organs internal medicine
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Research Institution | Keio University |
Principal Investigator |
EGASHIRA Toru 慶應義塾大学, 医学部, 研究員(非常勤) (10465023)
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Project Period (FY) |
2010 – 2011
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Project Status |
Completed (Fiscal Year 2011)
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Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2011: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2010: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
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Keywords | 循環器 / 遺伝性疾患 / モデル化 / iPS細胞 / トランスレーショナルリサーチ |
Research Abstract |
We generated iPS cells from patients with hypertrophic cardiomyopathy(HCM) and unaffected healthy volunteers. We also succeeded to differentiate generated iPS cells into cardiomyocytes in vitro reproducibly. Although we examined the various aspects of functional characteristics of iPS cells-derived cardiomyocytes and did not find those of significant differences in both cells, we clarified that the administration of X factor known as promoting cardiac hypertrophy highly induced cellular hypertrophy and disarray of alignment in structural proteins in HCM patient iPS cells-derived cardiomyocytes. Such phenomenon indicated that the difference of cellular response against X factor can contribute to onset of HCM.
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Report
(3 results)
Research Products
(15 results)
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[Journal Article] Wnt2 accelerates cardiac myocyte differentiation from ES-cell derived mesodermal cells via non-canonical pathway2012
Author(s)
Onizuka T, Yuasa S, Kusumoto D, Shimoji K, Egashira T, Ohno Y, Kageyama T, Tanaka T, Hattori R Fujita J, Ieda M, Kimura K, Makino S, Sano M, Kudo A, Fukuda K
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Journal Title
J Mol Cell Cardiol
Volume: 52(3)
Issue: 3
Pages: 650-9
DOI
Related Report
Peer Reviewed
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