Mechanisms of dental pulp stem cell differentiation into functional endothelium

牙髓干细胞分化为功能性内皮细胞的机制

• 批准号: 9897411
• 负责人: Jacques Eduardo Nor
• 金额: $ 37.05万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-07-01 至 2022-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9897411
• 关键词: ANGPT1 gene; Address; Anastomosis - action; Angiopoietins; Blood; Blood Vessels; Blood capillaries; Cell Communication; Cell Differentiation process; Cell Therapy; Cells; Data; Dental Pulp; Development; Embryo; Embryonic Development; Endothelial Cells; Endothelium; Event; Exhibits; Experimental Models; Funding; Generations; Goals; Hematopoietic stem cells; Human; Imaging Techniques; In Vitro; Investments; Maintenance; Mesenchymal Differentiation; Mesenchymal Stem Cells; Metabolic; Modeling; Molecular; Mus; Natural regeneration; Nutrient; Odontoblasts; Organ; Outcome; Oxygen; Paracrine Communication; Pathway interactions; Patients; Pericytes; Play; Process; Proto-Oncogene Protein c-kit; Receptor Protein-Tyrosine Kinases; Research Design; Role; Signal Pathway; Signal Transduction; Smooth Muscle Myocytes; Stem Cell Factor; Stem cell transplant; Structure; Testing; Therapeutic; Tissue Engineering; Tissues; Tooth structure; Undifferentiated; Up-Regulation; Vascular Endothelial Cell; Vascular Endothelial Growth Factor Receptor-1; Vascular Endothelial Growth Factors; Vascularization; Work; base; beta catenin; cadherin 5; clinical translation; clinically significant; design; experience; experimental study; in vivo; intercellular communication; postnatal; receptor; reconstitution; recruit; regenerative; self-renewal; stem cell biology; stem cell differentiation; stem cells; tissue regeneration; tissue repair; tool; vasculogenesis

PROJECT SUMMARY/ABSTRACT The Problem: Human dental pulps contain mesenchymal stem cells (MSC), i.e. dental pulp stem cells (DPSC) that orchestrate tooth development and tissue regeneration. In the 1st funding cycle, we showed that DPSC are capable of differentiating into endothelial cells that form functional blood vessels. These findings suggest that pluripotent DPSC can differentiate into tissue-forming cells (e.g. odontoblasts) while exhibiting the capacity to generate blood vessels to support the metabolic demands of tissue regeneration. However, the mechanisms employed by DPSC to generate blood vessels are unclear, and therefore our ability to exploit the differentiation potential of these cells in therapeutic tissue regeneration is limited. Hypothesis: We have shown that signaling initiated by vascular endothelial growth factor (VEGF) through its receptor VEGFR1, and by the canonical Wnt/B-catenin pathway, regulate the endothelial differentiation of DPSC. In preliminary studies, we made the exciting observation that DPSC-derived blood vessels anastomize with the host vasculature and become invested by smooth muscle cells/pericytes. However, the mechanisms regulating these events are not known. VE-Cadherin plays a key role in endothelial cell orientation, blood vessel organization and anastomosis during embryonic development. Once blood vessels are formed, the Angiopoietin/Tie2 pathway regulates vessel maturation. Here, we will determine if these signaling pathways play a role in the anastomosis and maturation of post-natal stem cell-derived blood vessels, using dental pulp stem cells as experimental models of MSC. Furthermore, it has been postulated that the long-term viability and function of tissues regenerated with MSC depends on the ability of these cells to reconstitute and maintain stem cell niches. Preliminary data suggest that endothelial cell-derived factors induce self-renewal of DPSC, as demonstrated by Bmi-1 upregulation and secondary sphere formation. Here, we will explore the role of the Stem Cell Factor (SCF)/c-Kit axis on the maintenance of stem cells in DPSC-regenerated tissues. Our working hypothesis is: “Blood vessels generated by endothelial differentiation of dental pulp stem cells anastomize with the host vasculature, mature upon mural cell investment, and maintain a pool of stem cells”. To test this hypothesis, we propose the following specific aims: S.A.#1: To define the role of VE-Cadherin on the anastomosis of DPSC-derived blood vessels; S.A.#2: To define the function of Angiopoietin signaling on the maturation of DPSC-derived blood vessels; S.A.#3: To define the role of the SCF/c-Kit pathway in the maintenance of stem cells in DPSC-generated tissues. Significance: The clinical translation of stem cell-based therapies requires the understanding of mechanisms that control the differentiation fate of these cells. Successful completion of this project will lead to mechanism- based therapies that exploit the vasculogenic potential of mesenchymal stem cells in tissue regeneration. The development of safe strategies that enable efficient vascularization of tissues generated upon transplantation of stem cells will benefit a large number of patients that require therapeutic tissue regeneration.

项目总结/摘要 问题：人类牙髓含有间充质干细胞（MSC），即牙髓干细胞（DPSC） 协调牙齿发育和组织再生。在第一个融资周期中，我们表明DPSC是 能够分化成形成功能性血管的内皮细胞。这些发现表明 多能DPSC可以分化成组织形成细胞（例如成牙本质细胞），同时表现出 生成血管以支持组织再生的代谢需求。然而，机制 DPSC用于产生血管的能力尚不清楚，因此我们利用DPSC分化血管的能力尚不清楚。 这些细胞在治疗性组织再生中的潜力有限。假设：我们已经证明， 由血管内皮生长因子（VEGF）通过其受体VEGFR 1启动， Wnt/B-catenin通路，调节DPSC的内皮分化。在初步研究中，我们 令人兴奋的观察是DPSC衍生的血管与宿主脉管系统融合， 由平滑肌细胞/周细胞包埋。然而，调节这些事件的机制尚不清楚。 VE-钙粘蛋白在内皮细胞定向、血管组织化和血管吻合中起关键作用。 胚胎发育一旦血管形成，血管生成素/Tie 2途径调节血管生成， 成熟在这里，我们将确定这些信号通路是否在吻合和成熟中发挥作用。 以牙髓干细胞作为MSC的实验模型，研究了新生儿干细胞来源的血管。 此外，已经假设用MSC再生的组织的长期存活力和功能 取决于这些细胞重建和维持干细胞小生境的能力。初步数据表明 内皮细胞衍生因子诱导DPSC自我更新，如Bmi-1上调所示， 次级球体形成。在这里，我们将探讨干细胞因子（SCF）/c-Kit轴在细胞凋亡中的作用。 维持DPSC再生组织中的干细胞。我们的工作假设是：“血管生成 牙髓干细胞通过内皮分化与宿主血管系统融合，在壁周成熟， 细胞投资，并维持干细胞库”。为了验证这一假设，我们提出了以下具体的 目标：S.A.# 1：确定VE-钙粘蛋白在DPSC衍生血管吻合中的作用; S.A.#第二章： 定义血管生成素信号传导对DPSC衍生的血管成熟的功能; S.A.# 3：向 确定SCF/c-Kit途径在DPSC产生的组织中维持干细胞的作用。 意义：基于干细胞的治疗的临床转化需要了解机制 控制着这些细胞的分化命运该项目的成功完成将导致机制- 在组织再生中利用间充质干细胞的血管生成潜力的基于治疗的方法。的 开发能够使移植后产生的组织有效血管化的安全策略 干细胞的应用将使大量需要治疗性组织再生的患者受益。