Vascular Precursors and Cell-Cell Signaling in Heart Vasculogenesis

心脏血管发生中的血管前体和细胞间信号传导

• 批准号: 9249631
• 负责人: Michael I. Kotlikoff
• 金额: $ 38.75万
• 依托单位: CORNELL UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-04-01 至 2019-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9249631
• 关键词: Acute; Adopted; Animals; Antigens; Area; Arrhythmia; Blood Vessels; Bone Marrow; Bone Marrow Cells; CXCR4 gene; Cardiac; Cardiac Myocytes; Cell Communication; Cell Therapy; Cell Transplantation; Cells; Clinical; Data; Development; Endothelial Cells; Fibrosis; Genetic; Genetic Recombination; Heart; Heart Injuries; Home environment; Homing; Human; In Vitro; Incidence; Infarction; Inflammatory; Injury; Knock-out; LacZ Genes; Letters; Ligands; LoxP-flanked allele; Maps; Marrow; Mesenchymal Stem Cells; Mitosis; Molecular; Mus; Myocardial Infarction; Myocardial Revascularization; PTPRC gene; Perfusion; Pericytes; Platelet-Derived Growth Factor alpha Receptor; Population; Process; Protein Tyrosine Kinase; Proto-Oncogene Protein c-kit; Publishing; Reaction; Receptor Protein-Tyrosine Kinases; Recovery of Function; Recruitment Activity; Role; Rosa; Signal Transduction; Site; Smooth Muscle; Smooth Muscle Myocytes; Stem Cell Factor; Stem cells; Stromal Cell-Derived Factor 1; Stromal Cells; Therapeutic; Tissues; Uncertainty; Vascularization; angiogenesis; cadherin 5; clinically significant; cytokine; experience; experimental study; functional improvement; genetic approach; heart cell; heart function; improved; in vivo; injury and repair; intercellular communication; neovascularization; paracrine; precursor cell; progenitor; public health relevance; repaired; therapeutic development; vasculogenesis; virtual

 DESCRIPTION (provided by applicant): There is increasing evidence that recovery of function following a heart attack is markedly influenced by revascularization of the infarcted region, which influences the extent of injury, the degree of fibrosis within the infarct, post injury remodeling, and the incidence of arrhythmia. Despite the importance of revascularization, the processes underlying angiogenesis and/or vasculogenesis remain poorly understood, including the degree to which precursor cells are involved in new vessel formation, the origin of these putative precursors (e.g. bone marrow or resident adventitial cells), and the signals that govern processes such as homing, fate, and endothelial cell (EC) mitosis. This proposal examines fundamental aspects of post-infarction revascularization in vivo, exploiting recent advances in the understanding and genetic specification of vascular precursors. Our central hypothesis is that infarction triggers the expansion and differentiation of endogenous vascular precursors that are induced through key heterotypic cell-cell interactions within the perivascular niche. The proposed experiments will identify the degree to which these precursors drive revascularization, determine their developmental origin, and establish the role of the expression of c-kit, SCF, Sca1, and SDF- 1¿/CXCR4 signaling in this process. Defined precursor populations and terminally differentiated vascular cells (endothelial and smooth muscle) will be genetically tagged and the lineage of post-infarct nascent vascular cells examined to determine the role of angiogenesis and vasculogenesis. The role of c-kit and its ligand stem cell factor (SCF), as well as other receptor tyrosine kinases, will be examined in conditionally deleted (SCF) mice. Heterotypic signaling functions of Sca1 cells that home to infarcts and are used for cell therapy, and the importance of cardiac and marrow CXCR4 signaling will be determined in knockout or conditionally inactivated mice. These experiments will establish a conceptual framework for the understanding of ischemic revascularization of the heart, a critical step in the development of therapeutic strategies directed toward enhancing vascular repair.

 描述（由申请人提供）：越来越多的证据表明，心脏病发作后的功能恢复明显受到梗死区域血运重建的影响，这会影响损伤程度、梗死内纤维化程度、损伤后重塑和心律失常的发生率。尽管血管重建的重要性，血管生成和/或血管发生的基础过程仍然知之甚少，包括前体细胞参与新血管形成的程度，这些推定的前体细胞（如骨髓或驻留外膜细胞）的起源，以及控制过程的信号，如归巢，命运和内皮细胞（EC）有丝分裂。该提案探讨了梗死后血管重建在体内的基本方面，利用血管前体的理解和遗传规范的最新进展。我们的中心假设是梗死触发了内源性血管前体的扩张和分化，这些血管前体是通过血管周围生态位内的关键异型细胞-细胞相互作用诱导的。拟议的实验将确定这些前体驱动血管重建的程度，确定其发育起源，并确定c-kit，SCF，Sca 1和SDF- 1？/CXCR 4信号传导在此过程中的表达作用。将对确定的前体细胞群和终末分化的血管细胞（内皮细胞和平滑肌细胞）进行基因标记，并检查梗死后新生血管细胞的谱系，以确定血管生成和血管发生的作用。c-kit及其配体干细胞因子（SCF）以及其他受体酪氨酸激酶的作用将在条件性缺失（SCF）小鼠中进行检查。将在敲除或条件灭活小鼠中确定归巢于梗死并用于细胞治疗的Sca 1细胞的异型信号传导功能，以及心脏和骨髓CXCR 4信号传导的重要性。这些实验将建立一个概念框架，了解缺血性心脏血运重建，一个关键的一步，在发展的治疗策略，旨在加强血管修复。