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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
翻译
描述(由申请人提供):房颤是人类最常见的心律失常,具有显著的发病率和死亡风险增加。缝隙连接通道可能在心房颤动的稳定和维持中发挥重要作用,因为心房颤动与心房肌细胞之间的连接重塑和电传导改变有关。这些通道(由连接蛋白亚基CX组成)提供了离子和小分子直接通过细胞间的途径,促进心脏电传导和心血管细胞对细胞内信号的反应协调。两种主要的连接蛋白(CX 40和CX 43)在心房中表达。大量研究表明,CX40的改变(包括水平降低、分布异质性和突变)有助于房颤的发病机制。提出了一系列的实验:(1)测试的假设,CX40单独或相对于CX43的改变存在于心房组织中的房颤患者,和(2)使用表达系统来测试这些改变如何影响细胞间通讯。实验结果将有助于阐明缝隙连接在心律失常中的作用。他们还将阐明缝隙连接介导的细胞间通讯的基本细胞生物学和生理学。
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)
专著(0)
科研奖励(0)
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