Stem Cells in the Developing Heart

发育中的心脏中的干细胞

基本信息

批准号：
7654403
负责人：
Marcello Rota
金额：
$ 41.9万
依托单位：
BRIGHAM AND WOMEN'S HOSPITAL
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-04-01 至 2014-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7654403
关键词：
1,2-diacylglycerol Abbreviations Actinin Actins Address Adult Affect Age Angiotensin II Anterior Antigens Biological Models Birth Calcium Calcium Channel Calcium Oscillations Calcium-Sensing Receptors Cardiac Cardiac Myocytes Cardiovascular Diseases Cell Differentiation process Cell Proliferation Cell division Cell physiology Cells Cellular Structures Complement Connexin 43 Contractile Proteins Coupled Data Development Differentiation and Growth Diglycerides Discrimination Elements Embryo Embryonic Heart Endoplasmic Reticulum Equation Event Fluorescence Gap Junctions Generations Goals Growth Heart Heart Atrium Homeostasis Human Hypertrophy ITPR1 gene In Vitro Inositol Insulin-Like Growth Factor I Insulin-Like-Growth Factor I Receptor Laboratories Lead Life Mechanics Mediating Mesoderm Methodology Mitotic Mitotic spindle Modeling Morphogenesis Mus Muscle Cells Muscle Contraction Myocardial Myosin Heavy Chains Organ Pattern Peptidyl-Dipeptidase A Phenotype Physiological Population Process Proliferating Property Proteins Proto-Oncogene Protein c-kit Published Comment Renin-Angiotensin System Research Role Ryanodine Receptor Calcium Release Channel Ryanodine Receptors Sarcoplasmic Reticulum Scheme Spatial Distribution Staging Stem cells Stretching System Time Transgenic Mice Ventricular Work Workload attenuation base calcium metabolism cell growth design fetal immunocytochemistry in vivo mechanical behavior migration mouse model postnatal prenatal primitive cell progenitor promoter public health relevance receptor regenerative repaired response transcription factor tripolyphosphate young adult

项目摘要

DESCRIPTION (provided by applicant): This application raises the possibility that the myocyte compartment of the embryonic, fetal and post-natal heart is generated by activation and lineage commitment of a pool of resident c-kit-positive cardiac progenitor cells (CPCs) which are clustered in niches within the primitive heart. Cardiac morphogenesis may be mediated by spontaneous calcium oscillations within CPCs which lead to cell growth and the acquisition of the myocyte phenotype. The possibility is raised that the fate of CPCs is regulated by transient changes in intracellular calcium which constitute the essential element of symmetric and asymmetric division of these primitive cells. Similarly, calcium oscillations condition the differentiation of CPCs into functionally competent myocytes which become electrically and mechanically excitable. To address these fundamental issues, two transgenic mouse models have been developed: one in which EGFP is under the control of the c-kit-promoter (c-kit-EGFP mouse) and the second in which EGFP expression is regulated by the cardiac specific 1-myosin heavy chain promoter (1MHC-EGFP mouse). The c-kit-EGFP mouse should allow us to identify the embryonic stages at which c-kit-positive-EGFP-positive CPCs appear in the forming heart, their anatomical distribution and developmental changes in prenatal and postnatal life. The 1MHC-EGFP mouse will permit us to define the localization and spatial distribution of forming myocytes postnatally and this information will be complemented with the data to be obtained in the c-kit-EGFP mouse. With these two models, the relationship between the generation of myocytes and the activation, commitment and differentiation of CPCs will be established. These studies will be integrated with the analysis of the electrophysiological, mechanical and calcium handling properties of CPCs and linearly related cells together with their pattern of growth and differentiation. Ultimately, the interdependence of cellular physiology and growth with calcium being the master regulatory system will be determined. Therefore, the role that intracardiac progenitor cells have in the developing heart will be characterized and this information may have important implications in the myocardial adaptations to ischemic and non-ischemic damage later in life. PUBLIC HEALTH RELEVANCE: Determining whether a selective class of stem cells is implicated in cardiac development has consequences on our understanding of the formation of the heart and the mechanisms that regulate muscle contraction. This information is critical for the identification of the regenerative potential of the adult heart and its ability to react and repair in response to cardiovascular disease.

描述（由申请人提供）：此应用程序提高了胚胎，胎儿和产后心脏的心肌室是通过激活和谱系的谱系承诺而产生的，这些居民C-KIT阳性心脏祖细胞（CPC）的谱系承诺在原始心脏内聚集了。心脏形态发生可能是由CPC内的自发钙振荡介导的，这会导致细胞生长和心肌细胞表型的获得。提出的可能性是，CPC的命运受细胞内钙的短暂变化的调节，这构成了这些原始细胞的对称和不对称分裂的基本元素。同样，钙振荡调节了CPC的分化为功能合理的心肌细胞，这些肌细胞变得具有电气和机械性。为了解决这些基本问题，已经开发了两种转基因小鼠模型：其中一个在C-KIT启动器（C-KIT-EGFP小鼠）的控制之下，第二种由心脏特异性1-肌动蛋白重链链促进剂（1MHC-EGFP小鼠）调节的第二种。 C-KIT-EGFP小鼠应该使我们能够识别C-kit阳性-EGFP阳性CPC出现在形成心脏中的胚胎阶段，它们的解剖学分布以及产后和产后寿命的发育变化。 1MHC-EGFP鼠标将允许我们在产后定义形成心肌细胞的定位和空间分布，并且该信息将与C-KIT-EGFP鼠标中要获得的数据相辅相成。通过这两个模型，将建立肌细胞产生与激活，承诺和分化之间的关系。这些研究将与CPC和线性相关细胞的电生理，机械和钙处理特性的分析以及它们的生长和分化模式集成。最终，将确定细胞生理学和生长的相互依赖性，而钙将确定主要调节系统。因此，心脏内祖细胞在发育中的心脏中具有的作用将被表征，并且该信息可能对心肌适应性对缺血性和非缺血性损害具有重要意义。公共卫生相关性：确定选择性类干细胞是否与心脏发育有关，对我们对心脏形成的理解以及调节肌肉收缩的机制有影响。该信息对于鉴定成人心脏的再生潜力及其对心血管疾病的反应和修复能力至关重要。