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Intercellular Communication in Microvessels

Intercellular Communication in Microvessels
微血管中的细胞间通讯
批准号:
6603886
负责人:
BRIAN R DULING
金额:
$29.6万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-01-01 至 2005-07-31

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中文摘要
翻译
在这个更新中,我们建议建立一个更机械的基础上的连接蛋白在微血管中的细胞间通讯的作用。 我们将研究小动脉中径向和纵向的细胞间通讯,强调平滑肌和内皮细胞通过肌内皮细胞连接结合形成一个功能单位。 该应用程序利用了我们在体外和体内系统中使用钙和电压成像的广泛理论和技术发展。 我们将系统地测试平滑肌和内皮细胞的钙池的联系赋予小动脉行为独特的反应模式的想法。 这个建议的一个独特的方面是一个比较研究的小动脉从三个物种已知有相当不同的小动脉反应。利用分子遗传学的工具,我们也开始了鉴定间隙连接通讯的特定分子贡献者的过程。 我们将包括实验连接蛋白37和40敲除和新开发的平滑肌和内皮细胞特异性敲除连接蛋白43。 我们试图回答三个广泛的问题。 首先,平滑肌和内皮细胞之间的细胞-细胞偶联如何调节小动脉的反应性? 第二,参与传导性血管反应的细胞间通路是什么? 第三,缝隙连接通讯在生理上重要吗? 几个相互关联的假设将被测试。 这些措施是:假设1 -膜电位和钙池的肌内皮偶联在确定对刺激的局部反应中起关键作用假设2 -膜电位变化的肌内皮偶联而不是内皮细胞钙的变化介导传导的血管反应假设3 -细胞-细胞偶联的类似途径在体外和体内存在假设4 -内皮作为染料和电耦合的优先途径发挥作用。假设5 -细胞间通讯由多种连接蛋白介导假设6-缝隙连接通讯在正常血管紧张度的建立中起作用
英文摘要
In this renewal we propose to establish a more mechanistic basis for the roles of the connexins in cell-cell communication in the microvasculature. We will study radial and longitudinal cell-cell communication in the arterioles, emphasizing the idea that the smooth muscle and the endothelial cell are united to form a functional unit via the myoendothelial cell junctions. The application takes advantage of our extensive theoretical and technical developments in the use of calcium and voltage imaging on in vitro and in vivo systems. We will systematically test the idea the linkage of the calcium pools of the smooth muscle and the endothelium confers unique response patterns on the behavior of arterioles. A unique aspect of this proposal is a comparative study of the arterioles from three species known to have quite different arteriolar responses. Using the tools of molecular genetics we have also begun the process of the process of identification of specific molecular contributors to gap junctional communication. We will include experiments on connexin 37 and 40 knockouts and newly developed smooth muscle and endothelial-cell specific knockouts of connexin 43. We seek to answer three broad questions. First, How does cell-cell coupling between smooth muscle and endothelial cell modulate arteriolar reactivity? Second, what are the intercellular pathways that are involved in the conducted vasomotor response? Third, is gap junctional communication physiologically important? Several interrelated hypotheses will be tested. These are: Hypothesis 1 - Myoendothelial coupling of both membrane potential and calcium pools play a critical role in determining local responses to stimulation Hypothesis 2 - Myoendothelial coupling of changes in membrane potential and not changes in the endothelial cell calcium mediate the conducted vasomotor responses Hypothesis 3 - Similar pathways for cell-cell coupling exist in vitro and in vivo Hypothesis 4 - The endothelium functions as a preferential pathway for dye and electrical coupling. Hypothesis 5 - Intercellular communication is mediated by multiple connexins Hypothesis 6- Gap junctional communication plays a role in the establishment of normal vasomotor tone
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Neutrophil Trafficking to Normal and Inflamed Lung
  • 批准号:
    7415117
  • 项目类别:
  • 资助金额:
    $27.39万
  • 财政年份:
    2007
  • 负责人:
    BRIAN R DULING
  • 依托单位:
Neutrophil Trafficking to Normal and Inflamed Lung
  • 批准号:
    7232630
  • 项目类别:
  • 资助金额:
    $18.03万
  • 财政年份:
    2006
  • 负责人:
    BRIAN R DULING
  • 依托单位:
Neutrophil Trafficking to Normal and Inflamed Lung
  • 批准号:
    7062084
  • 项目类别:
  • 资助金额:
    $17.5万
  • 财政年份:
    2005
  • 负责人:
    BRIAN R DULING
  • 依托单位:
Regulation of the Endothelial Cell Glycocalyx
  • 批准号:
    7350125
  • 项目类别:
  • 资助金额:
    $36.15万
  • 财政年份:
    2004
  • 负责人:
    BRIAN R DULING
  • 依托单位:
海外基金