Single cell hematopoietic fate acquisition during embryonic development: To be a stem cell or not?

胚胎发育过程中单细胞造血命运的获得：是否成为干细胞？

• 批准号: BB/S01845X/1
• 负责人: Elaine Dzierzak
• 金额: $ 82.92万
• 依托单位: University of Edinburgh
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2019
• 资助国家: 英国
• 起止时间: 2019 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=BB%2FS01845X%2F1
• 关键词: Single; cell; hematopoietic; fate; acquisition

Rare stem cells in the adult bone marrow are responsible for the healthy life-long production of all circulating blood cells. These stem cells are used in curative clinical transplantations for blood-related diseases and for cancer therapies. Although blood banks for such stem cells exist in the UK and worldwide, there are insufficient supplies of stem cells (high quality and large numbers of cells) for transplantations and importantly, the donor stem cells need to closely match the patient's cells to avoid graft rejection. For years, researchers have attempted to increase the number of blood stem cells in culture systems. However, blood stem cells obtained from adult bone marrow or umbilical cord blood do not retain their stem cell properties when cultured. Instead they mature into red blood cells, macrophages and immune cell types which are short-lived. Rather than furthering culture approaches to expand blood stem cells, a new reprogramming approach has been taken to generate new stem cells from skin cells and embryonic cells. To date, these reprogramming approaches have had very limited success. In my lab, discoveries in the mouse revealed that all blood stem cells are made early in the embryo from specialized (endothelial) cells lining the blood vessels. Importantly, blood stem cells are made only once during development. Our knowledge of blood stem cell development and the molecular program directing cells to become blood stem cells is fundamental to approaches aiming to generate patient-specific stem cells and for alleviating insufficient supplies of these cells for transplantation. This study aims to demonstrate the complete genetic program of blood stem cells as they are generated within the mouse embryonic aorta. The challenge is to identify the true blood stem cells, of which there are only 1-2 in the embryo amongst about 700 other types of blood cells. These other blood cells are very similar to blood stem cells but cannot repopulate the blood system following transplantation and thus are not curative. Because there is no current technology that allows the isolation of pure blood stem cells from the other blood cell types, we will isolate single cells from the mouse embryonic aorta using unique fluorescent reporters and test their function through transplantation. We will perform state-of-the-art single cell RNA sequencing experiments and use a new and highly innovative DNA marking technique to identify for the first time the complete genetic program that codes these unique functionally potent blood stem cells. This important information will further our understanding of how blood stem cells are made and advance strategies for generating robust patient specific stem cells for treatment of leukemia and hematologic disorders.

成人骨髓中的稀有干细胞负责所有循环血细胞的健康终身生产。这些干细胞用于血液相关疾病的临床治疗移植和癌症治疗。尽管在英国和世界各地都有储存此类干细胞的血库，但用于移植的干细胞（高质量和大量的细胞）供应不足，重要的是，供体干细胞需要与患者的细胞紧密匹配，以避免移植排斥反应。多年来，研究人员一直试图增加培养系统中血液干细胞的数量。然而，从成人骨髓或脐带血中获得的造血干细胞在培养时不能保留其干细胞特性。相反，它们成熟为红细胞、巨噬细胞和寿命较短的免疫细胞。而不是进一步培养方法来扩大血液干细胞，一种新的重编程方法已经被采用，从皮肤细胞和胚胎细胞产生新的干细胞。迄今为止，这些重编程方法取得的成功非常有限。在我的实验室里，在老鼠身上的发现表明，所有的血液干细胞都是在胚胎早期由血管内壁的特化（内皮）细胞形成的。重要的是，造血干细胞在发育过程中只产生一次。我们对血液干细胞发育和引导细胞成为血液干细胞的分子程序的了解，是旨在产生患者特异性干细胞和缓解这些细胞用于移植供应不足的方法的基础。本研究旨在证明血液干细胞在小鼠胚胎主动脉内生成的完整遗传程序。目前的挑战是鉴定真正的血液干细胞，在胚胎中大约700种其他类型的血细胞中只有1-2种。这些其他血细胞与血液干细胞非常相似，但在移植后不能重新填充血液系统，因此不能治愈。由于目前没有技术可以从其他类型的血细胞中分离出纯血液干细胞，我们将使用独特的荧光报告基因从小鼠胚胎主动脉中分离出单细胞，并通过移植测试其功能。我们将进行最先进的单细胞RNA测序实验，并使用一种新的高度创新的DNA标记技术，首次识别编码这些独特功能强大的血液干细胞的完整遗传程序。这一重要的信息将进一步加深我们对血液干细胞是如何产生的理解，并推进产生用于治疗白血病和血液疾病的患者特异性干细胞的策略。

项目成果

De novo hematopoietic (stem) cell generation - A differentiation or stochastic process?

• DOI: 10.1016/j.ceb.2023.102255
• 发表时间: 2023-10-06
• 期刊: CURRENT OPINION IN CELL BIOLOGY
• 影响因子: 7.5
• 作者: Vink，Chris S.;Popravko，Anna;Dzierzak，Elaine
• 通讯作者: Dzierzak，Elaine

Embryonic Origins of the Hematopoietic System: Hierarchies and Heterogeneity.

• DOI: 10.1097/hs9.0000000000000737
• 发表时间: 2022-06
• 期刊: HEMASPHERE
• 影响因子: 6.6
• 作者: Vink, Chris S.;Mariani, Samanta A.;Dzierzak, Elaine
• 通讯作者: Dzierzak, Elaine