课题基金 / 基金详情

项目摘要

项目成果

EMER MARIA SMYTH的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Vasoactive prostanoids and redox signaling are integral to cardiovascular physiology and disease. Principal amongst these mediators are prostacyclin (PGI2), predominantly cyclooxygenase (COX)-2-derived, and thromboxane (TxA2), the primary product of platelet COX-1. Opposition of TxA2 by PGI2 appears critical to cardiovascular homeostasis and pathophysiology - depression of PGI2 generation, with unrestricted biosynthesis of TxA2 provides a mechanistic explanation for the cardiovascular risk associated with selective COX-2 inhibitors. Biosynthesis of TxA2 and PGI2, and expression of their receptors, is augmented coincident with elevated reactive oxygen species (ROS) in cardiovascular disease. The dynamic interplay between these prostanoids appears to be mediated by complex interactions of their receptors and signaling events that they transduce. This proposal will investigate novel pathways through which redox signaling modulates the regulation, function and dimeric association of the receptors for TxA2 (the TP) and PGI2 (the IP). These studies will provide novel mechanistic insights into human cardiovascular disease. We will examine the convergence of TP and IP on redox signaling in three specific aims. Specific Aim 1 will define the mechanisms that drive a feed-froward loop, through which TP-derived ROS enhance TP expression, in vascular cells and in a mouse model of vascular injury. In Specific Aim 2, we will examine how IP-dependent modulation of TP can interrupt this loop. Finally, in Specific Aim 3, we propose to examine non-monomeric association of TP and IP, and the role of ROS in this process, as a regulator of receptor expression and function. Relevance to public health: The cardiovascular system has a series of check and balances designed to keep it functioning and prevent disease. This work will investigate one such system, examining novel mechanisms through which one mediator, prostacyclin, works to offsets the actions of another thromboxane, thus contributing to the maintenance of cardiovascular health.
期刊论文(8)
专著(0)
科研奖励(0)
会议论文
DOI: 10.2217/clp.10.11
发表时间: 2010-04-01
期刊: Clinical lipidology
影响因子: --
作者: [Smyth EM]
通讯作者: Smyth EM
DOI: 10.1161/atvbaha.110.208900
发表时间: 2010-09
期刊: Arteriosclerosis, thrombosis, and vascular biology
影响因子: --
作者: [Ibrahim S, Tetruashvily M, Frey AJ, Wilson SJ, Stitham J, Hwa J, Smyth EM]
通讯作者: Smyth EM
DOI: 10.1161/atvbaha.112.300536
发表时间: 2013-01
期刊: Arteriosclerosis, thrombosis, and vascular biology
影响因子: --
作者: [Ibrahim S, McCartney A, Markosyan N, Smyth EM]
通讯作者: Smyth EM
Activation-dependent stabilization of the human thromboxane receptor: role of reactive oxygen species.
人类血栓素受体的激活依赖性稳定:活性氧的作用。
DOI: 10.1194/jlr.m800447-jlr200
发表时间: 2009
期刊: Journal of lipid research
影响因子: 6.5
作者: [Wilson,StephenJ, Cavanagh,ClaireC, Lesher,AllisonM, Frey,AlexanderJ, Russell,ShaneE, Smyth,EmerM]
通讯作者: Smyth,EmerM
Regulation of Vascular Eicosanoid Receptors
  • 批准号:
    6547216
  • 项目类别:
  • 资助金额:
    $27.74万
  • 财政年份:
    2002
  • 负责人:
    EMER MARIA SMYTH
  • 依托单位:
Regulation of Vascular Eicosanoid Receptors
  • 批准号:
    6749012
  • 项目类别:
  • 资助金额:
    $27.74万
  • 财政年份:
    2002
  • 负责人:
    EMER MARIA SMYTH
  • 依托单位:
Regulation of Vascular Eicosanoid Receptors
  • 批准号:
    6640398
  • 项目类别:
  • 资助金额:
    $27.74万
  • 财政年份:
    2002
  • 负责人:
    EMER MARIA SMYTH
  • 依托单位:
Regulation of vascular eicosanoid receptors
  • 批准号:
    7467344
  • 项目类别:
  • 资助金额:
    $35.44万
  • 财政年份:
    2002
  • 负责人:
    EMER MARIA SMYTH
  • 依托单位:
国内基金
海外基金
Agonist-GPR119-Gs复合物的结构生物学研究
  • 批准号:
    32000851
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    24.0万元
  • 批准年份:
    2020
  • 负责人:
    乔安娜
  • 依托单位: