Embryonic Blood Vessel Formation
Embryonic Blood Vessel Formation
批准号:
7254844
负责人:
PAUL ANTHONY KRIEG
金额:
$32.21万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-07-01 至 2009-06-30
关键词:
AngioblastBiological ModelsBlood VesselsChick EmbryoDNADevelopmentEmbryoEmbryonic DevelopmentEphrinsErinaceidaeG-Protein-Coupled ReceptorsGene Transfer TechniquesGenetic TranscriptionGoalsGrowth FactorHumanInvestigationMesodermMesoderm CellMolecularNumbersOrganismPathway interactionsPatternPlayPrincipal InvestigatorProtein FamilyProtocols documentationRanaRegulationRegulatory ElementResearchRoleSignal PathwaySignal TransductionSignaling MoleculeSpecific qualifier valueTissuesTubeVascular Endothelial Growth Factor Receptor-2Vascular Endothelial Growth FactorsVascular SystemWound HealingXenopusdesigninnovationnotch proteinnovelprecursor cellprogramsrepairedresearch studysmoothened signaling pathwaytranscription factorvasculogenesis
中文摘要
描述(由申请人提供):本提案的研究重点是胚胎血管发育的分子和细胞机制。先前的研究表明,许多生长因子/信号分子在胚胎原始血管网络的形成过程中起着至关重要的作用。这些包括VEGF,血管生成素,特定的Notch通路成分和某些ephrins。用青蛙和鸡胚胎作为模型系统,我们有初步的证据表明两个额外的生长因子参与了胚胎血管发生的调节。首先,我们证明了刺猬家族蛋白的信号传导对血管的形成至关重要。其次,我们有证据表明,通过其g蛋白偶联受体APJ的apelin信号传导对血管系统的初始模式也很重要。该提案的两个具体目的是进一步探索这些信号通路在血管发育中的作用。最后,我们正在研究胚胎中原始血管内皮前体细胞(成血管细胞)的起源。我们建议通过确定哪些转录因子是表达最终成血管细胞标志物VEGFR-2(也称为ilk-1或KDR)所必需的,来确定成血管细胞形成的可能调节因子。本课题实验的具体目的如下:(1). 为了进一步表征hedgehog信号在血管发育中的作用,2)探索apelin信号在血管发育中的作用,(3)。鉴定成血管细胞中VEGFR-2表达所必需的DNA调控元件,从而确定哪些转录因子是定义成血管细胞谱系所必需的。
英文摘要
DESCRIPTION (provided by applicant): Research in this proposal focuses on the molecular and cellular mechanisms underlying embryonic vascular development. Previous studies have demonstrated that a number of growth factor/signaling molecules play essential roles during formation of the original blood vessel network in the embryo. These include VEGF, angiopoietin, specific Notch pathway components and also certain ephrins. Using the frog and chick embryos as model systems, we have preliminary evidence showing that two additional growth factors are involved in regulation of embryonic vasculogenesis. First, we show that signaling by hedgehog family proteins is essential for vascular tube formation. Second, we have evidence suggesting that apelin signaling through its G-protein coupled receptor, APJ, is also important for initial patterning of the vascular system. Two of the specific aims of this proposal are designed to further explore the role of these signaling pathways in vascular development. Finally, we are investigating the origin of the original vascular endothelial precursor cells (angioblasts) in the embryo. We propose to identify possible regulators of angioblast formation, by determining which transcription factors are required for expression of the definitive angioblast marker VEGFR-2 (also called ilk-1 or KDR). The specific aims of the experiments in the proposal are as follows; (1). To further characterize the function of hedgehog signaling in vascular development, 2) To explore the role of apelin signaling during vascular development, (3). To identify DNA regulatory elements essential for VEGFR-2 expression in angioblasts and thereby to determine which transcription factors are required for defining the angioblast lineage.
The long term goal of our research is to understand the molecular mechanisms underlying patterning and development of embryonic vascular tissues. Given the conservation of basic mechanisms underlying vertebrate development, it is extremely likely that results obtained using chick and frog embryos will be directly applicable to understanding formation of the embryonic vasculature in other organisms, including humans. This research has broad significance because the basic mechanisms underlying embryonic vascular development are likely to be reiterated during blood vessel formation associated with tumorogenesis, wound healing and vascular repair.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1002/cm.21029
发表时间:
2012-05
期刊:
Cytoskeleton (Hoboken, N.J.)
影响因子:
--
作者:
[Warkman AS, Whitman SA, Miller MK, Garriock RJ, Schwach CM, Gregorio CC, Krieg PA]
通讯作者:
Krieg PA
DOI:
10.1002/dvdy.22600
发表时间:
2011-06
期刊:
Developmental dynamics : an official publication of the American Association of Anatomists
影响因子:
--
作者:
[Moran CM, Salanga MC, Krieg PA]
通讯作者:
Krieg PA
Integration of repulsive guidance cues generates avascular zones that shape mammalian blood vessels.
DOI:
10.1161/circresaha.111.249847
发表时间:
2012-01-06
期刊:
Circulation research
影响因子:
20.1
作者:
[Meadows SM, Fletcher PJ, Moran C, Xu K, Neufeld G, Chauvet S, Mann F, Krieg PA, Cleaver O]
通讯作者:
Cleaver O
Regulation of Vascular Endothelial Gene Expression
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批准号:7851401
-
项目类别:
-
资助金额:$37.25万
-
财政年份:2009
-
负责人:PAUL ANTHONY KRIEG
-
依托单位:
Regulation of Vascular Endothelial Gene Expression
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批准号:7662586
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项目类别:
-
资助金额:$37.13万
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财政年份:2009
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负责人:PAUL ANTHONY KRIEG
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依托单位:
Embryonic Blood Vessel Formation
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批准号:6758669
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项目类别:
-
资助金额:$33.86万
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财政年份:2003
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负责人:PAUL ANTHONY KRIEG
-
依托单位:
Embryonic Blood Vessel Formation
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批准号:6894595
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项目类别:
-
资助金额:$33.86万
-
财政年份:2003
-
负责人:PAUL ANTHONY KRIEG
-
依托单位:
Embryonic Blood Vessel Formation
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批准号:6674438
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项目类别:
-
资助金额:$33.98万
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财政年份:2003
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负责人:PAUL ANTHONY KRIEG
-
依托单位:
Embryonic Blood Vessel Formation
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批准号:7064287
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项目类别:
-
资助金额:$33.18万
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财政年份:2003
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负责人:PAUL ANTHONY KRIEG
-
依托单位:
Commitment to the myocardial phenotype
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批准号:6609141
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项目类别:
-
资助金额:$28.8万
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财政年份:2002
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负责人:PAUL ANTHONY KRIEG
-
依托单位:
Commitment to the myocardial phenotype
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批准号:6493625
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项目类别:
-
资助金额:$28.8万
-
财政年份:2001
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负责人:PAUL ANTHONY KRIEG
-
依托单位:
Commitment to the myocardial phenotype
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批准号:6347075
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项目类别:
-
资助金额:$28.8万
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财政年份:2000
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负责人:PAUL ANTHONY KRIEG
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依托单位:
EMBRYONIC VASCULAR DEVELOPMENT
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批准号:6527510
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项目类别:
-
资助金额:$23.43万
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财政年份:1999
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负责人:PAUL ANTHONY KRIEG
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依托单位:
EMBRYONIC VASCULAR DEVELOPMENT
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批准号:2728629
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项目类别:
-
资助金额:$21.77万
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财政年份:1999
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负责人:PAUL ANTHONY KRIEG
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依托单位:
EMBRYONIC VASCULAR DEVELOPMENT
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批准号:6185039
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项目类别:
-
资助金额:$22.11万
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财政年份:1999
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负责人:PAUL ANTHONY KRIEG
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依托单位:
REGULATION OF MYOCARDIAL DEVELOPMENT
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批准号:2859941
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项目类别:
-
资助金额:$23.43万
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财政年份:1999
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负责人:PAUL ANTHONY KRIEG
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依托单位:
EMBRYONIC VASCULAR DEVELOPMENT
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批准号:6390705
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项目类别:
-
资助金额:$22.76万
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财政年份:1999
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负责人:PAUL ANTHONY KRIEG
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依托单位:
CARDIAC DEVELOPMENT
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批准号:2445281
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项目类别:
-
资助金额:$20.65万
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财政年份:1996
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负责人:PAUL ANTHONY KRIEG
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依托单位:
CARDIAC DEVELOPMENT
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批准号:2230326
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项目类别:
-
资助金额:$20.17万
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财政年份:1996
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负责人:PAUL ANTHONY KRIEG
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依托单位:
REGULATION OF GENE ACTIVITY IN XENOPUS EARLY DEVELOPMENT
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批准号:3326172
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项目类别:
-
资助金额:$21.37万
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财政年份:1990
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负责人:PAUL ANTHONY KRIEG
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依托单位:
REGULATION OF GENE ACTIVITY IN XENOPUS EARLY DEVELOPMENT
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批准号:3326174
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项目类别:
-
资助金额:$19.98万
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财政年份:1990
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负责人:PAUL ANTHONY KRIEG
-
依托单位:
REGULATION OF GENE ACTIVITY IN XENOPUS EARLY DEVELOPMENT
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批准号:3326173
-
项目类别:
-
资助金额:$19.02万
-
财政年份:1990
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负责人:PAUL ANTHONY KRIEG
-
依托单位:
REGULATION OF GENE ACTIVITY IN XENOPUS EARLY DEVELOPMENT
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批准号:3326175
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项目类别:
-
资助金额:$20.74万
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财政年份:1990
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负责人:PAUL ANTHONY KRIEG
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依托单位:
海外基金