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Stem cell biology in cardiovascular regeneration

Stem cell biology in cardiovascular regeneration
干细胞生物学在心血管再生中的应用
批准号:
7321642
负责人:
Manfred Boehm
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至

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中文摘要
翻译
心血管疾病(CVD),主要是心脏病和中风,是发达国家所有种族和族裔群体中男性和女性的主要死亡原因。这也是发展中国家面临的一个日益严重的问题。每年有近100万美国人死于CVD,约占所有死亡人数的42%。心血管疾病的并发症往往会导致长期的?长期而言,生活质量严重下降。心肌梗死后受损心脏愈合和新血管生长的能力有限是这些长期并发症,特别是心力衰竭的主要原因。我们的实验室专注于干细胞在心血管再生中的作用。我们正在从成年人的骨髓中分离稀有的干细胞群。这些被称为多能成体祖细胞(MAPCs)的细胞代表间充质基质细胞(MSC)的亚群,但具有能够分化成几乎所有身体组织的独特特性。当这些MAPCs被注射到发育中的小鼠胚胎中时,它们有助于所有器官结构(除了生殖系)的特性,使它们与胚胎干细胞相似,只是它们来自成年人,而不是胚胎。我们正在研究使MAPCs分化为内皮细胞和平滑肌细胞(正常血管中发现的主要细胞群)以及心肌细胞的分子机制。目前,我们正在大鼠和小鼠损伤模型中测试表征的MAPCs。我们已经在大鼠中开发了后肢缺血模型,并且正在测试和比较不同干细胞类型(MAPC、MSC和ES-细胞)在改善缺血后肢的灌注和功能方面的能力。了解干细胞的功能,包括分子和细胞途径,对于设计和开发心血管疾病的新疗法至关重要。我们预计,通过更好地了解这些成体干细胞的生物学及其在心脏再生中的作用,可能会开发新的治疗干预措施,以改善许多患有慢性心脏病的患者的预后。
英文摘要
Cardiovascular disease (CVD), principally heart disease and stroke, is the leading cause of death for both men and women, among all racial and ethnic groups in developed countries. It is also an increasing problem for developing countries. Almost 1 million Americans die of CVD each year, which is approximately 42% of all deaths. Complications of CVD often results in a long?term, severe reduction in quality of life. The limited ability of the damaged heart to heal, and of new blood vessels to grow after myocardial infarction are the main reasons for these long term complications, specifically of heart failure. Our laboratory focuses on the role of stem cells in cardiovascular regeneration. We are isolating rare stem cell populations from the bone marrow of adults. These cells called Multipotent Adult Progenitor Cells (MAPCs) represent a subpopulation of Mesenchymal Stromal Cells (MSC) but have the unique properties of being able to differentiate into almost all tissues of the body. When these MAPCs are injected into a developing mouse embryo, they contribute to all organ structures (except the germ line) properties that make them similar to embryonic stem cells except that they are derived from adults, not embryos. We are investigating the molecular mechanisms that enable MAPCs to differentiate into endothelial and smooth muscle cells, the major cell populations found in normal blood vessel, as well as cardiomyocytes. At present we are testing characterized MAPCs in rat and mouse injury models. We have developed a hind limb ischemia model in rats and are testing and comparing different stem cell types (MAPC, MSC and ES-cell) in their ability to improve not only the perfusion but also the function of ischemic hind limbs. Understanding the function including the molecular and cellular pathways of stem cells is critical to the design and development of new therapies for cardiovascular diseases. We anticipate that by better understanding the biology of these adult stem cells and their role in cardiac regeneration, new therapeutic interventions may be developed to improve the outcome of the many patients that suffer from chronic cardiac diseases.
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Underlying Mechanisms in CADASIL
Underlying Mechanisms in CADASIL
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