Notch Signaling in Vascular Development and Homeostasis
血管发育和稳态中的Notch信号传导
基本信息
- 批准号:7257474
- 负责人:
- 金额:$ 38.2万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2007
- 资助国家:美国
- 起止时间:2007-04-01 至 2012-03-31
- 项目状态:已结题
- 来源:
- 关键词:AblationAdultBiologicalBirthBlood VesselsCaliberCardiacCellsCessation of lifeConditionCongenital Heart DefectsDataDefectDevelopmentEmbryoEndothelial CellsEndotheliumEventExcisionExhibitsExperimental DesignsGene DeletionGenerationsGeneticGoalsHeartHemorrhageHomeostasisIn VitroKnock-outKnockout MiceLigandsLinkLiteratureMaintenanceMapsMediatingMolecularMorphogenesisMusMutant Strains MiceNotch Signaling PathwayNumbersPathologyPathway interactionsPatternPhenotypePublishingResearch PersonnelRoleSeriesSeveritiesShunt DeviceSignal PathwaySignal TransductionSmooth Muscle MyocytesStagingTestingTimeTissuesVascular SystemVenousWeekangiogenesisbaseconceptdayinsightinterestjagged1 proteinmouse modelmutantnotch proteinnovelprogramsreceptorrepairedresearch study
项目摘要
DESCRIPTION (provided by applicant): Our long-term goal is to gain a comprehensive understanding of the molecular programs required for the formation of blood vessels. A combination of genetic and cell biological data has established a critical role for Notch signaling in vascular morphogenesis. However, concrete mechanistic insight into Notch's cellular effects in vascular development and differentiation is still far reached. Deletion of Notch 1 results in early embryonic lethality (E.9.5) with multiple defects, including alterations in the heart and vessels. To gain a detailed understanding of Notch1 effects in the vascular compartment, we have generated a mouse model with endothelial-cell specific deletion of Notch1 using a Cre-lox strategy. As in the full deletion, this mouse dies between E9.5-10.5 from collapse of the vascular system, but does not exhibit somitic mesodermal defects and cardiac features seen after global inactivation. Mutant embryos displayed congenital aortic branch defects, reduced aortic lumen, aneurisms, arterial-venous shunts and deregulated vascular branching. We also generated an inducible Cre-lox mouse and subsequently deleted Notch at later developmental time points. Interestingly, ablation of Notch at E10.5 results in hemorrhage and lethality at E13.5. Furthermore, deletion of Notch at E15.5 also leads to multiple hemorrhagic events with lethality at birth. These findings support and expand our understanding of Notch and further highlight the exquisite requirement of this signaling pathway during vascular stabilization and maturation at later time-points. Our current focus is to gain a mechanistic understanding of Notch function at the cellular level and to establish the molecular links of these effects downstream of the Notch signaling pathway. By using a variety of mouse models and in vitro approaches, we propose: (1) to gain a mechanistic understanding of Notch1's effects during vascular development, (2) to explore the contribution of Notch1 in the homeostasis of adult vessels and in pathological conditions, and (3) to evaluate the contribution of Notch-ligand Jagged1 during development. The molecular mapping of vascular morphogenesis is critical to understanding how vessels are formed. Many of the events that take place during development are recapitulated in situations of neoangiogenesis and vascular repair in the adult. Thus, this information is central to the generation of novel and more effective therapies that will enable manipulation of vascular function during pathological conditions.
描述(由申请人提供):我们的长期目标是全面了解血管形成所需的分子程序。遗传和细胞生物学数据的组合已经确立了Notch信号在血管形态发生中的关键作用。然而,Notch在血管发育和分化中的细胞作用的具体机制仍远未达到。Notch 1的缺失导致早期胚胎死亡(E.9.5),伴有多种缺陷,包括心脏和血管的改变。为了详细了解Notch 1在血管区室中的作用,我们使用Cre-lox策略产生了内皮细胞特异性缺失Notch 1的小鼠模型。如在完全缺失中,该小鼠在E9.5-10.5之间死于血管系统的塌陷,但在整体失活后未表现出体节中胚层缺陷和心脏特征。突变胚胎表现出先天性主动脉分支缺陷,主动脉腔减少,动脉-静脉分流和血管分支失调。我们还产生了诱导型Cre-lox小鼠,随后在以后的发育时间点删除Notch。有趣的是,在E10.5时消融Notch导致E13.5时出血和死亡。此外,在E15.5处缺失Notch也导致出生时具有致死性的多个出血事件。这些发现支持并扩展了我们对Notch的理解,并进一步强调了在以后的时间点血管稳定和成熟过程中对该信号通路的精细要求。我们目前的重点是在细胞水平上获得对Notch功能的机制理解,并建立Notch信号通路下游这些效应的分子联系。通过使用各种小鼠模型和体外方法,我们提出:(1)获得Notch 1在血管发育过程中作用的机制理解,(2)探索Notch 1在成人血管稳态和病理条件下的贡献,以及(3)评估Notch配体Jagged 1在发育过程中的贡献。血管形态发生的分子图谱对于理解血管是如何形成的至关重要。在发育过程中发生的许多事件在成人的新血管生成和血管修复的情况下重演。因此,该信息对于产生新的和更有效的疗法是至关重要的,所述疗法将使得能够在病理状况期间操纵血管功能。
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)
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M. LUISA IRUELA-ARISPE其他文献
M. LUISA IRUELA-ARISPE的其他文献
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