Role of Id genes during cardiac development

Id 基因在心脏发育过程中的作用

• 批准号: 7365360
• 负责人: DIEGO FRAIDENRAICH
• 金额: $ 13.38万
• 依托单位: UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-06-01 至 2009-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7365360
• 关键词: Ablation; Address; Adult; BHLH Protein; Biological; Brain hemorrhage; Cardiac; Cells; Chimera organism; Communication; Complement; Congenital Heart Defects; Core Facility; Defect; Development; Differentiation Inhibitor; Embryo; Endocardium; Environment; Epicardium; Family; Gene Expression; Genes; Genomics; Goals; Heart; Helix-Turn-Helix Motifs; Histology; Injection of therapeutic agent; Institutes; LacZ Genes; Lead; Mediator of activation protein; Microinjections; Modeling; Molecular; Molecular Profiling; Mus; Mutation; Myocardial; Myocardium; Pathway interactions; Play; Protein Isoforms; Role; Signal Transduction; Skeletal system; Tissues; Transgenic Mice; Transgenic Model; Ventricular septum; angiogenesis; anticancer research; cardiogenesis; congenital heart disorder; embryonic stem cell; extracellular; inhibitor/antagonist; member; mutant; prevent; research study; stem; tissue culture; transcription factor

DESCRIPTION (provided by applicant): The goal of this proposal is to address the role of the Id (inhibitor of differentiation) genes in specific cardiac compartments during development. Idl, 2 and 3 are expressed in the developing heart in the developing epicardium, endocardium and endocardial cushions (ECs), but not in the myocardium. Idl, Id2 or Id3 gene ablation studies revealed no developmental defects, but Idlld3, Idl Id2 and Id21d3 double mutant embryos die by E13.5. Ablation of Idl-3 in varying combinations resulted in cardiac defects not only in the endocardium and in the ECs, but also in the myocardium, suggesting cross-communication between layers. Id deficient embryos displayed impaired trabeculae and interventricular septum, thin myocardial wall, stenotic outflow tract, disorganized endocardium and hypocellular ECs. Injection of LacZ-marked Embryonic Stem (ES) cells reversed the cardiac abnormalities and rescued the embryonic lethality of the Idlld3 KO embryos. Altered myocardial markers in the Id KO embryos are restored to normal in the mutant cells of the rescued hearts. Thus, The ES-derived cells display the capacity to reverse gene expression profiles in mutant cells in a non-cell autonomous fashion. These observations raise important biological questions: What is the role of Id in the epicardium, endocardium/EC and in the myocardium? Is the Id mode of action non-cell autonomous? Which are the Id-dependent signals involved in the cross-talk between cardiac layers? Aiming to answer these questions we propose to study the role of Id genes in adult hearts of rescued chimeras (AIM I), to study the requirement for Id genes in specific cardiac compartments (AIM II), and to identify key mediators of Id signaling (AIM III). We will use murine models to extend the studies conducted with ES cells. Additionally, we will generate conditional KO and tissue-specific transgenic models. Some of the experiments will be complemented by tissue culture studies. The Sloan-Kettering Institute for Cancer Research provides the appropriate environment required to carry out this project, including the mouse transgenic, genomics core, and histology core facilities. The long term goals are to develop murine models to better understand the role of developmental control genes in cardiac formation, how mutations in those genes lead to congenital heart disease, and how these abnormalities could be prevented or ameliorated by embryonic stem cell injection. These studies may have important implications for congenital heart disease.

描述（由申请人提供）： 该提案的目的是解决发育过程中特定心脏室中ID（分化抑制剂）基因的作用。 IDL，2和3在发育中的心外膜，心内膜和心内膜垫（EC）中表达，但在心肌中不表达。 IDL，ID2或ID3基因消融研究没有发现发育缺陷，但是IDLLD3，IDL ID2和ID21D3双突变胚胎死亡E13.5。 IDL-3在不同组合中的消融导致心脏缺陷不仅在心内膜和EC中，而且在心肌中也导致心脏缺陷，这表明层之间的交叉沟道。 ID缺陷的胚胎显示出受损的小梁和室内隔膜，薄的心肌壁，狭窄的流出道，杂乱无章的心内膜心脏和次细胞ECS。注射LACZ标记的胚胎（ES）细胞逆转心脏异常，并挽救了IDLLD3 KO胚胎的胚胎致死性。 ID KO胚胎中改变的心肌标记在被救出的心脏的突变细胞中恢复为正常。因此，ES衍生的细胞以非自主方式显示出突变细胞中逆转基因表达谱的能力。这些观察结果提出了重要的生物学问题：ID在心外膜，心内膜/EC和心肌中的作用是什么？ ID动作模式是非单元自主的吗？心脏层之间的串扰涉及哪些ID依赖性信号？旨在回答这些问题，我们建议研究ID基因在救出的嵌合体成人心脏中的作用（AIM I），研究对特定心脏隔室中ID基因的要求（AIM II），并识别ID信号的关键介体（AIM III）。我们将使用鼠模型扩展使用ES细胞进行的研究。此外，我们将生成有条件的KO和组织特异性的转基因模型。一些实验将由组织培养研究补充。斯隆 - 凯特林癌症研究所提供了执行该项目所需的适当环境，包括小鼠转基因，基因组学核心和组织学核心设施。长期目标是开发鼠模型，以更好地了解发育控制基因在心脏形成中的作用，这些基因中的突变如何导致先天性心脏病以及如何通过胚胎干细胞注射来预防或改善这些异常。这些研究可能对先天性心脏病具有重要意义。