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Connexons in Cardiovascular Cell Communication

Connexons in Cardiovascular Cell Communication
心血管细胞通讯中的连接子
批准号:
8486298
负责人:
ERIC C BEYER
金额:
$45.35万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-09-01 至 2015-05-31

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Atrial fibrillation is the most common arrhythmia in man and confers a significant morbidity and increased risk of mortality. Gap junction channels are likely to play significant roles in the stabilization and maintenance of atrial fibrillation, since atrial fibrillation is associated with remodeling of connections between atrial myocytes and altered electrical conduction. These channels (made of connexin subunits, CX) provide a pathway for direct intercellular passage of ions and small molecules facilitating cardiac electrical conduction and coordination of the responses of cardiovascular cells to intracellular signals. Two major connexins (CX40 and CX43) are expressed in the atrium. A variety of provocative studies suggest that alterations of CX40 (including reduced levels, heterogeneity of distribution, and mutations) contribute to the pathogenesis of atrial fibrillation. A series of experiments are proposed: (1) to test the hypothesis that alterations of CX40 alone or relative to CX43 are present in atrial tissue from patients with atrial fibrillation, and (2) to use expression systems to test how these alterations can affect intercellular communication. The results of the proposed experiments will clarify the role of gap junctions in cardiac arrhythmias. They will also elucidate the basic cellular biology and physiology of gap junction-mediated intercellular communication.
期刊论文(7)
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会议论文
DOI: 10.1093/cvr/cvs366
发表时间: 2013-03
期刊: Cardiovascular research
影响因子: 10.8
作者: [Jiajie Yan;W. Kong;Qiang Zhang;E. Beyer;G. Walcott;V. Fast;Xun Ai]
通讯作者: Jiajie Yan;W. Kong;Qiang Zhang;E. Beyer;G. Walcott;V. Fast;Xun Ai
A carboxyl terminal domain of connexin43 is critical for gap junction plaque formation but not for homo- or hetero-oligomerization.
connexin43 的羧基末端结构域对于间隙连接斑块的形成至关重要,但对于同源或异源寡聚化并不重要。
DOI: 10.1080/15419060390263092
发表时间: 2003
期刊: Cell communication & adhesion
影响因子: --
作者: [Martínez,AgustínD, Hayrapetyan,Volodya, Moreno,AlonsoP, Beyer,EricC]
通讯作者: Beyer,EricC
Intermittent hypoxia causes NOX2-dependent remodeling of atrial connexins.
间歇性缺氧会导致心房连接素的NOX2依赖性重塑。
DOI: 10.1186/s12860-016-0117-5
发表时间: 2017-01-17
期刊: BMC cell biology
影响因子: --
作者: [Gemel J, Su Z, Gileles-Hillel A, Khalyfa A, Gozal D, Beyer EC]
通讯作者: Beyer EC
Institutional Career Development Core (Chapter 1)
  • 批准号:
    9528026
  • 项目类别:
  • 资助金额:
    $63.23万
  • 财政年份:
    2017
  • 负责人:
    ERIC C BEYER
  • 依托单位:
I. Institutional Career Development Core
  • 批准号:
    10632160
  • 项目类别:
  • 资助金额:
    $98.71万
  • 财政年份:
    2017
  • 负责人:
    ERIC C BEYER
  • 依托单位:
Institutional Career Development Core (Chapter 1)
  • 批准号:
    10206312
  • 项目类别:
  • 资助金额:
    $62.93万
  • 财政年份:
    2017
  • 负责人:
    ERIC C BEYER
  • 依托单位:
I. Institutional Career Development Core
  • 批准号:
    10673807
  • 项目类别:
  • 资助金额:
    $98.51万
  • 财政年份:
    2017
  • 负责人:
    ERIC C BEYER
  • 依托单位:
海外基金