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

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.

摘要 从成纤维细胞直接对诱导的心肌细胞(ICM)进行心脏重编程已成为一种 治疗心力衰竭的有希望的治疗策略，心力衰竭仍然是死亡和死亡的主要原因 发达国家的发病率。虽然关于从小鼠细胞产生的ICM已知很多，但 直接心脏重编程适应人类细胞的效率和质量都很低 因为物种之间的内在差异。我们最近报道了单细胞转录分析 在人类心脏重新编程期间，发现ICM的生成不足与 与不发达的基因程序，如离子通道和细胞连接，表明额外的 可能需要重新编程调节心肌细胞功能的因子。在这个研究项目中，我们 一种新的重编程因子TBX20在产生心肌细胞特性中起重要作用的假说 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，我们的 初步数据显示，在人类ICM中，TBX20在很大程度上表达不足。虽然强迫表达 在激活基因程序的同时，显著提高了重编程效率 与心肌细胞功能有关。为了检验这一假设，我们建议1)进一步确定影响 TBX20对人类心脏直接重编程的影响和2)确定TBX20如何作为必需的 在这一过程中的重新编程因素。这项建议的主要目标是确定 Tbx20对心脏直接重编程过程中心肌细胞再生的影响。这项工程的完成 该提案不仅提供了对心肌细胞身份如何通过直接 心脏重新编程，也使我们能够直接从人类产生功能可靠的心肌细胞 非心肌细胞用于潜在的心脏修复。

项目成果

Cardiomyocyte Cell-Cycle Regulation in Neonatal Large Mammals: Single Nucleus RNA-Sequencing Data Analysis via an Artificial-Intelligence-Based Pipeline.

• DOI: 10.3389/fbioe.2022.914450
• 发表时间: 2022
• 期刊: FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY
• 影响因子: 5.7
• 作者: Nguyen, Thanh;Wei, Yuhua;Nakada, Yuji;Zhou, Yang;Zhang, Jianyi
• 通讯作者: Zhang, Jianyi

A review of protocols for human iPSC culture, cardiac differentiation, subtype-specification, maturation, and direct reprogramming.

• DOI: 10.1016/j.xpro.2022.101560
• 发表时间: 2022-09-16
• 期刊: STAR PROTOCOLS
• 作者: Lyra-Leite, Davi M.;Gutierrez-Gutierrez, Oscar;Wang, Meimei;Zhou, Yang;Cyganek, Lukas;Burridge, Paul W.
• 通讯作者: Burridge, Paul W.