心脏分化路线图分析可塑性和平衡谱系承诺。

IF 5.1 2区 医学 Q1 CELL & TISSUE ENGINEERING
Stem Cell Reports Pub Date : 2025-03-11 Epub Date: 2025-02-27 DOI:10.1016/j.stemcr.2025.102422
Rebecca R Snabel, Carla Cofiño-Fabrés, Marijke Baltissen, Verena Schwach, Robert Passier, Gert Jan C Veenstra
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引用次数: 0

摘要

基于干细胞的人类心脏组织和心脏分化模型采用具有不同性质、细胞类型组成和成熟度的单层和三维类器官培养物。在这里,我们展示了心脏单层,胚胎样体和工程心脏组织轨迹在心房和心室分化条件的单细胞路线图中的比较。使用多组学方法和基因调控网络推断,我们确定了心外膜、心房和心室心肌细胞谱系的调控因子。我们确定ZNF711是心肌细胞承诺的调节开关和保障。我们发现,在缺乏维甲酸的情况下,ZNF711消融可阻止心肌细胞分化,导致祖细胞更明显地转移到心外膜和其他谱系。维甲酸挽救了谱系承诺的这种转变,并通过调节共享和互补的靶基因促进心房心肌细胞分化,表明ZNF711和维甲酸在心脏谱系承诺中存在相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiac differentiation roadmap for analysis of plasticity and balanced lineage commitment.

Stem cell-based models of human heart tissue and cardiac differentiation employ monolayer and 3D organoid cultures with different properties, cell type composition, and maturity. Here we show how cardiac monolayer, embryoid body, and engineered heart tissue trajectories compare in a single-cell roadmap of atrial and ventricular differentiation conditions. Using a multiomic approach and gene-regulatory network inference, we identified regulators of the epicardial, atrial, and ventricular cardiomyocyte lineages. We identified ZNF711 as a regulatory switch and safeguard for cardiomyocyte commitment. We show that ZNF711 ablation prevents cardiomyocyte differentiation in the absence of retinoic acid, causing progenitors to be diverted more prominently to epicardial and other lineages. Retinoic acid rescues this shift in lineage commitment and promotes atrial cardiomyocyte differentiation by regulation of shared and complementary target genes, showing interplay between ZNF711 and retinoic acid in cardiac lineage commitment.

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来源期刊
Stem Cell Reports
Stem Cell Reports CELL & TISSUE ENGINEERING-CELL BIOLOGY
CiteScore
10.50
自引率
1.70%
发文量
200
审稿时长
28 weeks
期刊介绍: Stem Cell Reports publishes high-quality, peer-reviewed research presenting conceptual or practical advances across the breadth of stem cell research and its applications to medicine. Our particular focus on shorter, single-point articles, timely publication, strong editorial decision-making and scientific input by leaders in the field and a "scoop protection" mechanism are reasons to submit your best papers.
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