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2006 Fiscal Year Final Research Report Summary

Investigation of the molecular mechanisms of cardiac failure focusing on the Z-disc abnormalities

Research Project

Project/Area Number 16390219
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Circulatory organs internal medicine
Research InstitutionTokyo 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)

Project Period (FY) 2004 – 2006
Keywordshypertrophic 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.

  • Research Products

    (26 results)

All 2007 2006 2005 2004

All Journal Article (26 results)

  • [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
    • Journal Title

      Int J Cardiol 116(2)

      Pages: 263-265

    • Description
      「研究成果報告書概要(和文)」より
  • [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
    • 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
  • [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
    • Journal Title

      Int J Cardiol 116(2)

      Pages: 263-265

    • Description
      「研究成果報告書概要(欧文)」より
  • [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
    • 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
  • [Journal Article] alphaB-crystallin in mutation in dilated cardiomyopathy2006

    • Author(s)
      Inagaki N, Hayashi T, Arimura T, Koga Y, Takahashi M, Shibata H, Teraoka K, Chikamori T, Yamashina A, Kimura A
    • Journal Title

      Biochem Biophys Res Commun 342(2)

      Pages: 379-386

    • Description
      「研究成果報告書概要(和文)」より
  • [Journal Article] Direct determination of SNP haplotype of NFKBIL1 promoter polymorphism by DNA conformation analysis and its application to association study of chronic inflammatory diseases2006

    • Author(s)
      Shibata H, Yasunami M, Obuchi N, Takahashi M, Kobayashi Y, Numano F, Kimura A
    • Journal Title

      Hum Immunol 67(4-5)

      Pages: 363-373

    • Description
      「研究成果報告書概要(和文)」より
  • [Journal Article] AlphaB-crystallin in mutation in dilated cardiomyopathy.2006

    • Author(s)
      Inagaki N, Hayashi T, Arimura T, Koga Y, Takahashi M, Shibata H, Teraoka K, Chikamori T, Yamashina A, Kimura A
    • Journal Title

      Biochem Biophys Res Commun 342(2)

      Pages: 379-386

    • Description
      「研究成果報告書概要(欧文)」より
  • [Journal Article] Direct determination of SNP haplotype of NFKBIL1 promoter polymorphism by DNA conformation analysis and its application to association study of chronic inflammatory diseases.2006

    • Author(s)
      Shibata H, Yasunami M, Obuchi N, Takahashi M, Kobayashi Y, Numano F, Kimura A
    • Journal Title

      Hum Immunol 67(4.5)

      Pages: 363-373

    • Description
      「研究成果報告書概要(欧文)」より
  • [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
    • Journal Title

      Int J Cardiol 99(2)

      Pages: 343-345

    • Description
      「研究成果報告書概要(和文)」より
  • [Journal Article] Spontaneous T wave alterans in a patient with Brugada syndrome-responses to intravenous administration of class I antiarrhythmic drug, glucose tolerance test, and atrial pacing2005

    • Author(s)
      Nishizaki M, Fujii H, Sakurada H, Kimura A, Hiraoka M
    • Journal Title

      J. Cardiovasc Electrophysiol 16

      Pages: 217-220

    • Description
      「研究成果報告書概要(和文)」より
  • [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
    • 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
  • [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
    • Journal Title

      Tissue Antigens 66(3)

      Pages: 200-208

    • Description
      「研究成果報告書概要(和文)」より
  • [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
    • 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
  • [Journal Article] Spontaneous T wave alterans in a patient with Brugada syndrome--responses to intravenous administration of class I antiarrhythmic drug, glucose tolerance test, and atrial pacing.2005

    • Author(s)
      Nishizaki M, Fujii H, Sakurada H, Kimura A, Hiraoka M
    • Journal Title

      J Cardiovasc Electrophysiol 16

      Pages: 217-220

    • Description
      「研究成果報告書概要(欧文)」より
  • [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
    • 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
  • [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
    • Journal Title

      Tissue Antigens 66(3)

      Pages: 200-208

    • Description
      「研究成果報告書概要(欧文)」より
  • [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
    • 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
  • [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
    • Journal Title

      J Biol Chem 279(26)

      Pages: 27194-27198

    • Description
      「研究成果報告書概要(和文)」より
  • [Journal Article] Unexpected mexiletine responses of a mutant cardiac Na+ channel implicate the selectivity filter as a structural determinant of antiarrhythmic drug access2004

    • Author(s)
      Sasaki K, Makita N, Sunami A, Sakurada H, Shirai N, Yokoi H, Kimura A, Tohse N, Hiraoka M, Kitabatake A
    • Journal Title

      Mol Pharmacol 66

      Pages: 330-336

    • Description
      「研究成果報告書概要(和文)」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
    • Journal Title

      FEBS Lett 574(1-3)

      Pages: 145-150

    • Description
      「研究成果報告書概要(和文)」より
  • [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
    • 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
  • [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
    • 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
  • [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
    • 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
    • Journal Title

      FEBS Lett 574(1.3)

      Pages: 145-150

    • Description
      「研究成果報告書概要(欧文)」より
  • [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
    • 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

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Published: 2008-05-27  

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