TGF-b family signaling in cardiomyocyte differentiation from embryonic stem cells

胚胎干细胞向心肌细胞分化中的 TGF-b 家族信号传导

• 批准号: 7738990
• 负责人: RIK M DERYNCK
• 金额: $ 23.18万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-01 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7738990
• 关键词: Activins; Affect; Autocrine Communication; Cardiac; Cardiac Myocytes; Cell Culture Techniques; Cell Nucleus; Cell Therapy; Cells; Characteristics; DNA Binding; Developmental Biology; Engraftment; Family; Gene Expression; Gene Targeting; Generations; Genetic Transcription; Goals; Heart; Individual; Knowledge; Lead; Lentivirus Vector; Ligands; Mediator of activation protein; Methods; Mus; Myocardial; Myocardial Infarction; Myocardial tissue; Myocardium; Natural regeneration; Pathway interactions; Phosphorylation; Play; Process; Property; Protein Family; Proteins; Quality Control; Regulation; Reporting; Research; Role; Signal Pathway; Signal Transduction; Source; Stimulus; System; Testing; Tissue Differentiation; Tissues; Vertebrates; autocrine; base; cell type; design; embryonic stem cell; human embryonic stem cell; improved; in vivo; inhibitor/antagonist; insight; interest; knock-down; mouse model; overexpression; paracrine; pluripotency; progenitor; public health relevance; receptor; repaired; research study; response; self-renewal; small hairpin RNA; stem cell differentiation; tissue regeneration; transcription factor

DESCRIPTION (provided by applicant): There is considerable interest in cell-based therapies for the repair and tissue regeneration of myocardial tissue. Embryonic stem cells are explored as an unlimited source of cells for cardiac repair, as they can differentiate into cardiomyocytes in culture. A better understanding of the regulation of this differentiation process would greatly aid in the generation of cardiomyocytes, and may lead to methods to improve the yield, control the quality and homogeneity, and direct subtype characteristics of the cardiomyocytes. Little is known about the signaling pathways and transcription factors that control the differentiation potential and cardiomyocyte differentiation of human embryonic stem cells. Oct4, Sox2 and Nanog function as essential transcription factors for self-renewal and pluripotency, yet may also play key roles in the initiation of differentiation into cardiomyocytes. Signaling by TGF-2 family proteins controls self-renewal, pluripotency and differentiation of stem cells, and autocrine signaling by TGF-2 family proteins is likely to play a key role in the self-renewal and differentiation of embryonic stem cells. TGF-2 family proteins exert gene expression responses through Smads, which enhance or repress the transcription activities of transcription factors at target genes, and thus function as cell-intrinsic mediators of differentiation. Through this mode of action, Smads are likely to regulate the expression levels and functions of embryonic stem cell transcription factors, such as Oct4, Sox2 and Nanog, and regulate the selection and progression of differentiation of cardiomyocytes from embryonic stem cells. The overall goals of this proposal are to (1) evaluate the regulation of expression and activities of the Oct4, Sox2 and Nanog by TGF-2 family/Smad signaling, (2) correlate this level of control with the differentiation potential and characteristics of differentiation along the cardiomyocyte lineage, (3) to use this knowledge to generate cardiomyocyte progenitors with high efficiency and defined characteristics. We hypothesize that (1) Smad signaling by TGF-2 family proteins regulates the expression and activities of the embryonic stem cell transcription factors, (2) alterations in Smad signaling and Oct4, Sox2 and/or Nanog activities modify the differentiation capacity of the cells and specifically cardiomyocyte differentiation. We propose three Aims: (1) to examine the regulation of embryonic stem cell transcription factor expression and activities by TGF-2 family signaling and to correlate these findings with cardiomyocyte lineage differentiation, (2) to study the roles of individual Smads in the regulation of Oct4, Sox2 and Nanog, and the roles of these Smads and Oct4, Sox2 and Nanog themselves in cardiomyocyte lineage differentiation, (3) To examine the in vivo differentiation and tissue integration characteristics of cardiomyocyte precursors derived from embryonic stem cells following manipulations that favor the generation of these cells in culture. PUBLIC HEALTH RELEVANCE: Cell-based therapies for the repair and tissue regeneration of heart tissue, for example following heart infarct, may provide great promise, and human embryonic stem cells are being considered as a cello source for these cells, called cardiomyocytes. We now propose a research plan in which we try to understand signaling pathways that may direct the differentiation of cardiomyocytes. We will explore how to modify these pathways and hope to design approaches that increase and improve the generation and characteristics of the cardiomyocytes. This will be tested through a combination of cell culture experiments and a new method in which the cardiomyocytes are injected into the heart muscle of mice with a heart infarct.

描述（由申请人提供）：对心肌组织的修复和组织再生的基于细胞的疗法有很大的兴趣。胚胎干细胞被探索为心脏修复的无限细胞来源，因为它们可以区分培养中的心肌细胞。更好地了解这种分化过程的调节将极大地有助于产生心肌细胞，并可能导致提高产量，控制质量和同质性以及直接亚型特征的方法。关于控制人类胚胎干细胞的分化潜力和心肌细胞分化的信号通路和转录因子知之甚少。 Oct4，Sox2和Nanog充当自我更新和多能性的基本转录因子，但在分化为心肌细胞中的启动中也可能起关键作用。 TGF-2家族蛋白的信号传导控制干细胞的自我更新，多能性和分化以及TGF-2家族蛋白的自分泌信号传导可能在胚胎干细胞的自我更新和分化中起关键作用。 TGF-2家族蛋白通过SMADS发挥基因表达反应，从而增强或抑制靶基因的转录因子的转录活性，从而充当分化的细胞内介介质。通过这种作用方式，SMAD可能会调节胚胎干细胞转录因子的表达水平和功能，例如OCT4，SOX2和NANOG，并调节从胚胎干细胞中心肌细胞分化的选择和进展。该提案的总体目标是（1）评估TGF-2家族/SMAD信号传导OCT4，SOX2和NANOG对表达和活动的调节，（2）将这种控制水平与沿心肌细胞谱系的分化潜力和分化的特征相关联（3），（3）使用此知识来实现​​较高的心肌细胞质量和较高的效率和定义的效率和定义。我们假设（1）TGF-2家族蛋白SMAD信号传导调节胚胎干细胞转录因子的表达和活性，（2）SMAD信号传导和OCT4，SOX2和/或NANOG活性的改变可修饰细胞的分化能力以及特定的心脏模板分化。 We propose three Aims: (1) to examine the regulation of embryonic stem cell tr​​anscription factor expression and activities by TGF-2 family signaling and to correlate these findings with cardiomyocyte lineage differentiation, (2) to study the roles of individual Smads in the regulation of Oct4, Sox2 and Nanog, and the roles of these Smads and Oct4, Sox2 and Nanog themselves in cardiomyocyte lineage分化，（3）检查体内分化和组织整合特性的伴有胚胎干细胞的心肌前体的操纵，这些操纵有利于在培养中产生这些细胞。公共卫生相关性：基于细胞的心脏组织修复和组织再生的疗法，例如心脏梗死，可能会提供巨大的前景，人类胚胎干细胞被视为这些细胞的大提琴来源，称为心肌细胞。现在，我们提出了一个研究计划，我们试图了解可能指导心肌细胞区分的信号通路。我们将探索如何修改这些途径，并希望设计方法来增加和改善心肌细胞的产生和特征。这将通过细胞培养实验和一种新方法的结合来测试，其中将心肌细胞注射到具有心脏梗塞的小鼠的心肌中。