Critical Role of TBX20 in Cardiomyocyte Maturation during Direct Cardiac Reprogramming

TBX20 在直接心脏重编程过程中心肌细胞成熟中的关键作用

• 批准号: 10662347
• 负责人: Yang Zhou
• 金额: $ 37.13万
• 依托单位: UNIVERSITY OF ALABAMA AT BIRMINGHAM
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-08-25 至 2024-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10662347
• 关键词: Affect; Binding; Biological Assay; Calcium; Cardiac; Cardiac Myocytes; Cells; Chromatin; Cicatrix; Computer Analysis; Data; Dermal; Developed Countries; Development; Family; Fibroblasts; Future; Gene Activation; Gene Expression Profiling; Generations; Genes; Genetic; Genetic Transcription; Genomics; Heart; Heart Injuries; Heart failure; Histones; Human; Image; In Situ; In Vitro; Injury; Intercellular Junctions; Ion Channel; Left ventricular structure; Maps; Membrane; Molecular; Morbidity - disease rate; Mus; Myocardial Infarction; Myocardial Ischemia; Myofibrils; Natural regeneration; Neonatal; Optics; Patients; Performance; Play; Process; Proliferating; Regulation; Reporting; Research; Residual state; Role; Route; Sarcomeres; Structure; System; Technology; Testing; Therapeutic; Time; Tissues; Transactivation; Transmission Electron Microscopy; cardiac repair; clinical application; clinical translation; cofactor; epigenomics; genetic signature; in vivo; inducible gene expression; insight; loss of function; mortality; mouse model; multiple omics; novel; overexpression; penis foreskin; programs; protein expression; single-cell RNA sequencing; stem cell differentiation; transcription factor; transcriptome; transcriptomics; treatment strategy; tumorigenesis; voltage; Affect; Binding; Biological Assay; Calcium; Cardiac; Cardiac Myocytes; Cells; Chromatin; Cicatrix; Computer Analysis; Data; Dermal; Developed Countries; Development; Family; Fibroblasts; Future; Gene Activation; Gene Expression Profiling; Generations; Genes; Genetic; Genetic Transcription; Genomics; Heart; Heart Injuries; Heart failure; Histones; Human; Image; In Situ; In Vitro; Injury; Intercellular Junctions; Ion Channel; Left ventricular structure; Maps; Membrane; Molecular; Morbidity - disease rate; Mus; Myocardial Infarction; Myocardial Ischemia; Myofibrils; Natural regeneration; Neonatal; Optics; Patients; Performance; Play; Process; Proliferating; Regulation; Reporting; Research; Residual state; Role; Route; Sarcomeres; Structure; System; Technology; Testing; Therapeutic; Time; Tissues; Transactivation; Transmission Electron Microscopy; cardiac repair; clinical application; clinical translation; cofactor; epigenomics; genetic signature; in vivo; inducible gene expression; insight; loss of function; mortality; mouse model; multiple omics; novel; overexpression; penis foreskin; programs; protein expression; single-cell RNA sequencing; stem cell differentiation; transcription factor; transcriptome; transcriptomics; treatment strategy; tumorigenesis; voltage

SUMMARY Direct cardiac reprogramming to generated induced cardiomyocytes (iCMs) from fibroblasts has emerged as a promising therapeutic strategy for the treatment of heart failure, which is still the leading cause of mortality and morbidity in the developed country. While much is known regarding iCMs generated from mouse cells, the adaptation of direct cardiac reprogramming to human cells is hurdled with low efficiency and poor quality because of intrinsic differences between species. We recently reported the single cell transcriptomic analysis during human cardiac reprogramming and discovered that the insufficient generation of iCMs is associated with underdeveloped gene programs, such as ion channel and cell junction, suggesting that additional reprogramming factors regulating function of cardiomyocytes might be required. In this research program, we hypothesis that a novel reprogramming factor TBX20 plays an essential role to generate cardiomyocyte identity by establishing gene programs associated with cardiomyocyte function. In support of our hypothesis, our preliminary data have shown that TBX20 is largely under-expressed in human iCMs. While forced expression of TBX20 significantly enhanced reprogramming efficiency accompanied with activation of gene programs associated with cardiomyocyte function. To test the hypothesis, we propose to 1) further determine the impact of TBX20 on direct human cardiac reprogramming and 2) determine how TBX20 functions as an essential reprogramming factor during this process. The main objective of this proposal is to identify the critical role of TBX20 on regeneration of cardiomyocytes during direct cardiac reprogramming. The completion of this proposal will not only provide mechanistic insight into how cardiomyocyte identity can be regenerated by direct cardiac reprogramming but also enable us to generate functional-reliable cardiomyocytes directly from human non-myocytes for potential heart repair.

概括 直接对成纤维细胞产生的诱导心肌细胞（ICM）的心脏重编程已成为一种 有希望治疗心力衰竭的治疗策略，这仍然是死亡率和 发达国家的发病率。虽然对从小鼠细胞产生的ICMS有很多了解，但 直接心脏重编程对人类细胞的适应性低效率和质量差。 由于物种之间的内在差异。我们最近报道了单细胞转录组分析 在人类心脏重新编程期间，发现ICM的产生不足 与离子通道和细胞连接等欠发达的基因程序有关，这表明了其他 可能需要调节心肌细胞功能的重编程因子。在这个研究计划中，我们 假设新型重编程因子TBX20起产生心肌细胞身份的重要作用 通过建立与心肌细胞功能相关的基因程序。为了支持我们的假设 初步数据表明，在人类ICM中，TBX20在很大程度上表现不足。而强迫表达 TBX20的重新编程效率显着提高，并伴随着基因程序的激活 与心肌细胞功能相关。为了检验假设，我们提议1）进一步确定影响 在直接人类心脏重编程中的TBX20和2）确定TBX20的作用是必不可少的 在此过程中重新编程因子。该提案的主要目的是确定 TBX20在直接心脏重编程过程中心肌细胞再生。完成此完成 提案不仅将提供有关如何通过直接再生心肌细胞身份的机械洞察 心脏重新编程，但也使我们能够直接从人身上产生可靠的功能可靠的心肌细胞 非肌细胞潜在的心脏修复。