Novel vascular guidance mechanisms
新型血管引导机制
基本信息
- 批准号:7730449
- 负责人:
- 金额:$ 37.63万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2004
- 资助国家:美国
- 起止时间:2004-07-01 至 2013-06-30
- 项目状态:已结题
- 来源:
- 关键词:AcuteAcute Lung InjuryAdaptor Signaling ProteinAdult Respiratory Distress SyndromeAge related macular degenerationAlveolarAngiogenic FactorAnimal ModelBacterial ModelBiological AssayBleomycinBlindnessBlood VesselsBlood capillariesCardiovascular systemCell CommunicationCell Culture TechniquesCellsClinicalCloningComplexDeveloped CountriesDeveloping CountriesDiseaseDominant-Negative MutationEdemaEndothelial CellsEndotheliumEndotoxinsEpithelialEquilibriumEye diseasesFaceFamilyFundingGIT1 geneGrantGrowth FactorHomeostasisInfectionInflammationInflammatoryInflammatory ResponseInfluenza A Virus, H5N1 SubtypeInjuryIntercellular JunctionsIschemiaLigandsLinkLiquid substanceLungMeasuresMediatingModelingMolecularMonomeric GTP-Binding ProteinsMorbidity - disease rateNatural regenerationNutrientPathologicPathologyPathway interactionsPermeabilityProcessProteinsReportingRetinalRetinal DiseasesRoleSignal PathwaySignal TransductionSmall Interfering RNASwellingTestingTubeVascular Endothelial Growth FactorsVascular EndotheliumVascular SystemWarWaterangiogenesisaptamerbasecadherin 5capillarycell motilitycytokinediabeticin vivoin vivo Modelmacular edemamembermigrationmortalitynovelpaxillinpreventprogramsprotein protein interactionpublic health relevancereceptorrelating to nervous systemresearch studyresponsesmall moleculesrc-Family Kinases
项目摘要
DESCRIPTION (provided by applicant): The equilibrium between stability and regeneration is critical to maintaining a functional vasculature. In the mature circulatory system, the endothelium provides critical barrier and regulatory functions by controlling fluid, nutrient and cellular transport between intravascular and extravascular compartments. Vascular injury induces an inflammatory response that stimulates the release of cytokines and growth factors. These factors weaken endothelial cell-cell junctions, stimulate migration and proliferation, and pave the way for remodeling and regeneration. Thus, there is constant tug-of-war within the vascular endothelium between signals that maintain vascular homeostasis/stability and signals that incite regeneration/instability. The central hypothesis for this competitive renewal is that Slit-Robo4 is an endogenous ligand receptor pathway that drives the balance toward homeostasis/stability. If this model is correct, then Robo4 signal might oppose the destabilizing influences of injury, ischemia, and inflammation mediated by a variety of angiogenic and inflammatory cytokines. Specific Aim 1: Elucidate the mechanism of Robo4 signaling. Specific Aim 2: Determine whether Slit-Robo4 is a broad platform for blunting the vascular response to cytokines. At the conclusion of our studies, we hope our contribution will be to demonstrate that Robo4 is a broad vascular stabilization program and to define its downstream signaling cascade. PUBLIC HEALTH RELEVANCE: At the conclusion of our studies, we hope our contribution will be to demonstrate that Robo4 is a broad vascular stabilization program and to define its downstream signaling cascade. In pursuing these objectives we hope to demonstrate that activating this vascular stability program will reduce pathologic endothelial hyperpermeability in a variety of ischemic and inflammatory diseases.
描述(由申请人提供):稳定性和再生之间的平衡对于维持功能性血管系统至关重要。在成熟的循环系统中,内皮细胞通过控制血管内和血管外室之间的液体、营养物质和细胞的运输,提供关键的屏障和调节功能。血管损伤会引发炎症反应,刺激细胞因子和生长因子的释放。这些因素削弱内皮细胞-细胞连接,刺激迁移和增殖,并为重塑和再生铺平道路。因此,在血管内皮细胞中,维持血管动态平衡/稳定的信号和刺激再生/不稳定的信号之间存在着持续的拉锯战。这种竞争性更新的中心假设是Sit-Robo4是一条内源性配体受体途径,推动平衡走向动态平衡/稳定。如果这个模型是正确的,那么Robo4信号可能会对抗由各种血管生成和炎症细胞因子介导的损伤、缺血和炎症的不稳定影响。具体目的1:阐明Robo4信号转导机制。具体目标2:确定Sit-Robo4是否是钝化血管对细胞因子的反应的广泛平台。在我们的研究结论中,我们希望我们的贡献将是证明Robo4是一个广泛的血管稳定程序,并确定其下游信号级联。公共卫生相关性:在我们的研究结论中,我们希望我们的贡献将是证明Robo4是一个广泛的血管稳定计划,并定义其下游信号级联。在追求这些目标的过程中,我们希望证明,激活这一血管稳定性计划将降低各种缺血性和炎症性疾病的病理性内皮细胞高通透性。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
DEAN Yaw LI其他文献
DEAN Yaw LI的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('DEAN Yaw LI', 18)}}的其他基金
Identifying a nodal point for G alpha q signaling in eye disease
确定眼部疾病中 G α q 信号传导的节点
- 批准号:
9006784 - 财政年份:2016
- 资助金额:
$ 37.63万 - 项目类别:
Endothelial Toll-Like Receptor Signaling and Inflammation
内皮 Toll 样受体信号转导和炎症
- 批准号:
8577458 - 财政年份:2014
- 资助金额:
$ 37.63万 - 项目类别:
Endothelial Toll-Like Receptor Signaling and Inflammation
内皮 Toll 样受体信号转导和炎症
- 批准号:
8794450 - 财政年份:2014
- 资助金额:
$ 37.63万 - 项目类别:
High Content Sceening for Hereditary Stroke Syndrome
遗传性中风综合症的高内涵筛查
- 批准号:
8577461 - 财政年份:2013
- 资助金额:
$ 37.63万 - 项目类别:
The Role of the Vasculature in the Pathogenesis of Arthritis
脉管系统在关节炎发病机制中的作用
- 批准号:
8685891 - 财政年份:2013
- 资助金额:
$ 37.63万 - 项目类别:
The Role of the Vasculature in the Pathogenesis of Arthritis
脉管系统在关节炎发病机制中的作用
- 批准号:
8560103 - 财政年份:2013
- 资助金额:
$ 37.63万 - 项目类别:
High Content Sceening for Hereditary Stroke Syndrome
遗传性中风综合症的高内涵筛查
- 批准号:
8731282 - 财政年份:2013
- 资助金额:
$ 37.63万 - 项目类别:
High Content Sceening for Hereditary Stroke Syndrome
遗传性中风综合症的高内涵筛查
- 批准号:
8920675 - 财政年份:2013
- 资助金额:
$ 37.63万 - 项目类别:
The Development of Screening Assays For Novel Inhibitors Of ARNO And Its Effector
新型ARNO抑制剂及其效应物筛选方法的研究进展
- 批准号:
8544183 - 财政年份:2012
- 资助金额:
$ 37.63万 - 项目类别:
相似海外基金
Combinatorial cytokine-coated macrophages for targeted immunomodulation in acute lung injury
组合细胞因子包被的巨噬细胞用于急性肺损伤的靶向免疫调节
- 批准号:
10648387 - 财政年份:2023
- 资助金额:
$ 37.63万 - 项目类别:
Lung epithelial cell-derived C3 in acute lung injury
肺上皮细胞衍生的 C3 在急性肺损伤中的作用
- 批准号:
10720687 - 财政年份:2023
- 资助金额:
$ 37.63万 - 项目类别:
Examining the role of TRMT1 and tRNA methylation in acute lung injury and ARDS
检查 TRMT1 和 tRNA 甲基化在急性肺损伤和 ARDS 中的作用
- 批准号:
10719249 - 财政年份:2023
- 资助金额:
$ 37.63万 - 项目类别:
Inducible HMGB1 antagonist for viral-induced acute lung injury.
诱导型 HMGB1 拮抗剂,用于治疗病毒引起的急性肺损伤。
- 批准号:
10591804 - 财政年份:2023
- 资助金额:
$ 37.63万 - 项目类别:
MAP2K1 AND MAP2K2 IN ACUTE LUNG INJURY AND RESOLUTION
MAP2K1 和 MAP2K2 在急性肺损伤中的作用及缓解
- 批准号:
10741574 - 财政年份:2023
- 资助金额:
$ 37.63万 - 项目类别:
Development of a new treatment for COVID-19-related acute lung injury targeting the microbiota-derived peptide corisin
针对微生物群衍生肽 corisin 开发治疗 COVID-19 相关急性肺损伤的新疗法
- 批准号:
23K07651 - 财政年份:2023
- 资助金额:
$ 37.63万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Probing immunovascular mechanobiology in pneumonia-associated acute lung injury at the single capillary level
在单毛细血管水平探讨肺炎相关急性肺损伤的免疫血管力学生物学
- 批准号:
10679944 - 财政年份:2023
- 资助金额:
$ 37.63万 - 项目类别:
The amyloid precursor protein protects against acute lung injury
淀粉样前体蛋白可预防急性肺损伤
- 批准号:
10575258 - 财政年份:2023
- 资助金额:
$ 37.63万 - 项目类别:
Role of macrophages and miRNA in regulating lung macrophage polarization and lung pathogenesis during respiratory virus-induced acute lung injury in normal and diabetic Syrian hamsters.
正常和糖尿病叙利亚仓鼠呼吸道病毒引起的急性肺损伤期间巨噬细胞和 miRNA 在调节肺巨噬细胞极化和肺部发病机制中的作用。
- 批准号:
10701207 - 财政年份:2023
- 资助金额:
$ 37.63万 - 项目类别:
Roles of N-glycans on neutrophil beta2 integrins in progression of acute lung injury
N-聚糖对中性粒细胞β2整合素在急性肺损伤进展中的作用
- 批准号:
10837431 - 财政年份:2023
- 资助金额:
$ 37.63万 - 项目类别: