2006 Fiscal Year Final Research Report Summary
Investigation of the molecular mechanisms of cardiac failure focusing on the Z-disc abnormalities
Project/Area Number |
16390219
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Circulatory organs internal medicine
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Research Institution | Tokyo Medical and Dental University |
Principal Investigator |
KIMURA Akinori Tokyo Medical and Dental University, Medical Research Institute, Professor, 難治疾患研究所, 教授 (60161551)
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Project Period (FY) |
2004 – 2006
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Keywords | hypertrophic cardiomyopathy / dilated cardiomyopathy / mutation / pathogenesis / calcium sensitivity / stretch response / metabolic stress response / myosin light chain |
Research Abstract |
Heart failure is a disease condition defined by insufficient cardiac output required for oxygen supply. Causes of the most severe heart failure include hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM). We have identified disease genes for HCM and/or DCM and suggested the linkage between the heart failure, and abnormality in Z-disc function. In this study, we aimed to identify the Z-disc abnormalities associated with heart failure and to reveal the molecular mechanisms of heart failure caused by the Z-disc abnormalities as well as to obtain a strategy to suppress the abnormal function of Z-disc. Main topics were as follows. (1) TCAP mutations were found in the patients with HCM and mutations in TCAP, CRYAB and FHL2 were, found in the patients with DCM. In addition MYPN mutation was found in restrictive cardiomyopathy, (RCM). TCAP, CRYAB, FHL2 and MYPN encoded components of Z-band or I-band, further supporting the pathological roles of abnormalities in the Z-I band function. (2) TTN mutations impaired interaction with FHL2 and CRYAB, suggesting the interaction of TTN with FHL2 and CRYAB was important for cardiac muscle function. (3) MYPN mutation found in RCM impaired formation of myofibrils in rat cardiomyocytes, suggesting the functional role of MYPN in cardiac sarcomerogenesis. (4) Cypher/ZASP bound to a metabolic enzyme and Cyper/ZASP mutations disrupted this interaction, and the metabolic enzyme was found to localized into Z-I band region upon stress to cardiomyocytes. These findings suggested a novel function of Z-band. (5) M21, a small inhibitory subunit of PP1M, increased calcium sensitivity of cardiac muscle contraction, and M21-overexpressing transgenic mice showed sudden death and cardiac hypertrophy accompanied by myocyte-disarrays, which were closely similar to the clinical observations in HCM. The M21-transgenic mice would be a good animal model for HCM and indicated that the increased calcium sensitivity was the cause of HCM.
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Research Products
(26 results)
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[Journal Article] Human cardiac ryanodine receptor mutations in ion channel disorders in Japan2007
Author(s)
Aizawa Y, Mitsuma W, Ikrar T, Komura S, Hanawa H, Miyajima S, Miyoshi F, Kobayashi Y, Chinushi M, Kimura A, Hiraoka M, Aizawa Y
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Journal Title
Int J Cardiol 116(2)
Pages: 263-265
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy2007
Author(s)
Arimura T, Hayashi T, Matsumoto Y, Shibata H, Hiroi S, Nakamura T, Inagaki N, Hinohara K, Takahashi M, Itoh-Satoh M, Bonne G, Schwartz K, Kimura A
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Journal Title
Biochem Biophys Res Commun 46(6)
Pages: 285-289
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Human cardiac ryanodine receptor mutations in ion channel disorders in Japan.2007
Author(s)
Aizawa Y, Mitsuma W, Briar T, Komura S, Hanawa H, Miyajima S, Miyoshi F, Kobayashi Y, Chinushi M, Kimura A, Hiraoka M, Aizawa Y
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Journal Title
Int J Cardiol 116(2)
Pages: 263-265
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy.2007
Author(s)
Arimura T, Hayashi T, Matsumoto Y, Shibata H, Hiroi S, Nakamura T, Inagaki N, Hinohara K, Takahashi M, Itoh-Satoh M, Bonne G, Schwartz K, Kimura A
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Journal Title
Biochem Biophys Res Commun 357(1)
Pages: 162-167
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] A novel mutation in FKBP12.6 binding region of the human cardiac ryanodine receptor gene (R2401H) in Japanese patient with catecholaminergic polymorphic ventricular tachycardia2005
Author(s)
Aizawa Y, Ueda K, Komura S, Washizuka T, Chinushi M, Inagaki N, Matsumoto Y, Hayashi T, Takahashi M, Nakano N, Yasunami M, Kimura A, Hiraoka M, Aizawa Y
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Journal Title
Int J Cardiol 99(2)
Pages: 343-345
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Lifelong left ventricular remodeling of hypertrophic cardiomyopathy caused by a founder frameshift deletion mutation in the cardiac myosin-binding protein C gene2005
Author(s)
Kubo T, Kitaoka H, Okawa M, Matsumura Y, Hitomi N, Yamazaki N, Furuno T, Takata J, Nishinaga M, Kimura A, Doi YL
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Journal Title
J Am Coll Cardiol 46(9)
Pages: 1737-1743
Description
「研究成果報告書概要(和文)」より
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[Journal Article] The haplotype block, NFKBIL1-ATP6V1G2-BAT1-MICB-MICA, within the class III-class I boundary region of the human major histocompatibility complex may control susceptibility to hepatitis C virus associated dilated cardiomyopathy2005
Author(s)
Shichi D, Kikkawa FE, Ota M, Katsuyama Y, Kimura A, Matsumori A, Kulsky JK, Naruse KT, Inoko H
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Journal Title
Tissue Antigens 66(3)
Pages: 200-208
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Functional analysis of titin/connectin N2-B mutations found in cardiomyopathy2005
Author(s)
Matsumoto Y, Hayashi T, Inagaki N, Takahashi M, Hiroi S, Nakamura T, Arimura T, Nakamura K, Ashizawa N, Yasunami M, Ohe T, Yano K, Kimura A
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Journal Title
J Muscle Res Cell Motil 26(6-8)
Pages: 367-374
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Lifelong left ventricular remodeling of hypertrophic cardiomyopathy caused by a founder frameshift deletion mutation in the cardiac myosin-binding protein C gene.2005
Author(s)
Kubo T, Kitaoka H, Okawa M, Matsumura Y, Hitomi N, Yamazaki N, Furuno T, Takata J, Nishinaga M, Kimura A, Doi YL
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Journal Title
J Am Coll Cardiol 46(9)
Pages: 1727-1743
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] The haplotype block, NFKBIL1-ATP6V1G2-BAT1-MICB-MICA, within the class III-class I boundary region of the human major histocompatibility complex may control susceptibility to hepatitis C virus associated dilated cardiomyopathy.2005
Author(s)
Shichi D, Kikkawa FE, Ota M, Katsuyama Y, Kimura A, Matsumori A, Kulsky JK, Naruse KT, Inoko H
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Journal Title
Tissue Antigens 66(3)
Pages: 200-208
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Functional analysis of titin/connectin N2-B mutations found in cardiomyopathy.2005
Author(s)
Matsumoto Y, Hayashi T, Inagaki N, Takahashi M, Hiroi S, Nakamura T, Arimura T, Nakamura K, Ashizawa N, Yasunami M, Ohe T, Yano K, Kimura A
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Journal Title
J Muscle Res Cell Motil 26(6.8)
Pages: 367-374
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia2004
Author(s)
Ueda K, Nakamura K, Hayashi T, Inagaki N, Takahashi M, Arimura T, Morita H, Higashiuesata Y, Hirano Y, Yasunami M, Takishita S, Yamashina A, Ohe T, Sunamori M, Hiraoka M, Kimura A
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Journal Title
J Biol Chem 279(26)
Pages: 27194-27198
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Truncated KCNQ1 mutant, A178fs/105, forms hetero-multimer channel with wild-type causing a dominant-negative suppression due to trafficking2004
Author(s)
Aizawa Y, Ueda K, Wu LM, Inagaki N, Hayashi T, Takahashi M, Ohta M, Kawano S, Hirano Y, Yasunami M, Aizawa Y, Kimura A, Hiraoka M
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Journal Title
FEBS Lett 574(1-3)
Pages: 145-150
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Novel C-terminus frameshift mutation, 1122fs/147, of HERG in LQT2 : additional amino acids generated by frameshift cause accelerated inactivation2004
Author(s)
Sasano T, Ueda K, Orikabe M, Hirano Y, Kawano S, Yasunami M, Isobe M, Kimura A, Hiraoka M
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Journal Title
J Mol Cell Cardiol 37(6)
Pages: 1205-1211
Description
「研究成果報告書概要(和文)」より
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[Journal Article] TCAP mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy2004
Author(s)
Hayashi T, Arimura T, Itoh-Satoh M, Ueda K, Hohda S, Inagaki, N, Takahashi M, Hori H, Yasunami M, Nishi H, Koga Y, Nakamura H, Matsuzaki M, Cho BY, Bae SW, You CW, Han KH, Park JE, Knoll R, Hoshijima M, Chien KR, Kimura A
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Journal Title
J Am Col Cardiol 44(11)
Pages: 2192-2201
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia.2004
Author(s)
Ueda K, Nakamura K, Hayashi T, Inagaki N, Takahashi M, Arimura T, Morita H, Higashiuesata Y, Hirano Y, Yasunami M, Takishita S, Yamashina A, Ohe T, Sunamori M, Hiraoka M, Kimura A
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Journal Title
J Biol Chem 279(26)
Pages: 27194-27198
Description
「研究成果報告書概要(欧文)」より
-
[Journal Article] Truncated KCNQ1 mutant, A178fs/105, forms hetero-multimer channel with wild-type causing a dominant-negative suppression due to trafficking2004
Author(s)
Aizawa Y, Ueda K, Wu LM, Inagaki N, Hayashi T, Takahashi M, Ohta M, Kawano S, Hirano Y, Yasunami M, Aizawa Y, Kimura A, Hiraoka M
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Journal Title
FEBS Lett 574(1.3)
Pages: 145-150
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Novel C-terminus frameshift mutation, 1122fs/147, of HERG in LQT2: additional amino acids generated by frameshift cause accelerated inactivation.2004
Author(s)
Sasano T, Ueda K, Orikabe M, Hirano Y, Kawano S, Yasunami M, Isobe M, Kimura A, Hiraoka M
-
Journal Title
J Mol Cell Cardiol 37(6)
Pages: 1205-1211
Description
「研究成果報告書概要(欧文)」より
-
[Journal Article] TCAP mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy2004
Author(s)
Hayashi T, Arimura T, Itoh-Satoh M, Ueda K, Hohda S, Inagaki, N, Takahashi M, Hori H, Yathimami M, Nishi H, Koga Y, Nakamura H, Matsuzaki M, Cho BY, Bae SW, You CW, Han KH, Park JE, Knoll R, Hoshijima M, Chien KR, Kimura A
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Journal Title
J AM Col Cardiol 44(11)
Pages: 2192-2201
Description
「研究成果報告書概要(欧文)」より