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(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相当大的兴趣。胚胎干细胞被认为是心脏修复的无限细胞来源，因为它们可以在培养中分化为心肌细胞。更好地了解这种分化过程的调控将大大有助于心肌细胞的产生，并可能导致提高心肌细胞产量、控制心肌细胞的质量和均质性以及直接确定心肌细胞亚型特征的方法。目前对控制人胚胎干细胞分化潜能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是细胞自我更新和多能性所必需的转录因子，但也可能在启动向心肌细胞分化的过程中发挥关键作用。转化生长因子-2家族蛋白的信号转导调控干细胞的自我更新、多能性和分化，而转化生长因子-2家族蛋白的自分泌信号转导可能在胚胎干细胞的自我更新和分化中起关键作用。转化生长因子-2家族蛋白通过Smads发挥基因表达反应，增强或抑制靶基因转录因子的转录活性，从而发挥细胞内源性分化介质的作用。通过这种作用方式，Smads可能调节胚胎干细胞转录因子Oct4、Sox2和Nanog的表达水平和功能，并调控胚胎干细胞向心肌细胞分化的选择和进展。该方案的总体目标是：(1)评估转化生长因子-2家族/Smad信号对Oct4、Sox2和Nanog表达和活性的调节；(2)将这种调控水平与心肌细胞系的分化潜能和分化特征相关联；(3)利用这一知识来产生高效和明确特征的心肌祖细胞。我们推测：(1)通过转化生长因子-2家族蛋白的Smad信号调节胚胎干细胞转录因子的表达和活性，(2)Smad信号和Oct4、Sox2和/或Nanog活性的改变改变了细胞的分化能力，特别是心肌细胞的分化。我们提出了三个目标：(1)检测转化生长因子-2家族信号对胚胎干细胞转录因子表达和活性的调节，并将这些结果与心肌细胞系分化相关；(2)研究单个Smads在Oct4、Sox2和Nanog调控中的作用，以及这些Smads和Oct4、Sox2和Nanog自身在心肌细胞系分化中的作用；(3)检测胚胎干细胞来源的心肌前体细胞在体内的分化和组织整合特征。公共卫生相关性：基于细胞的心脏组织修复和组织再生疗法，例如在心肌梗死后，可能提供巨大的前景，人类胚胎干细胞被认为是这些细胞的细胞来源，称为心肌细胞。我们现在提出一个研究计划，试图了解可能指导心肌细胞分化的信号通路。我们将探索如何修改这些途径，并希望设计出增加和改善心肌细胞的生成和特性的方法。这将通过细胞培养实验和一种将心肌细胞注射到心肌梗死小鼠的心肌中的新方法来进行测试。