Cardiac conduction system regeneration prevents arrhythmias after myocardial infarction

被引:3
作者
Sayers, Judy R. [1 ,2 ]
Martinez-Navarro, Hector [3 ]
Sun, Xin [1 ,2 ]
de Villiers, Carla [1 ,2 ]
Sigal, Sarah [1 ,2 ]
Weinberger, Michael [1 ,2 ]
Rodriguez, Claudio Cortes [1 ,2 ]
Riebel, Leto Luana [3 ]
Berg, Lucas Arantes [3 ]
Camps, Julia [3 ]
Herring, Neil [2 ]
Rodriguez, Blanca [3 ]
Sauka-Spengler, Tatjana [4 ,5 ]
Riley, Paul R. [1 ,2 ]
机构
[1] Univ Oxford, Inst Dev & Regenerat Med, Oxford, England
[2] Univ Oxford, Dept Physiol Anat & Genet, Oxford, England
[3] Univ Oxford, British Heart Fdn, Ctr Res Excellence, Dept Comp Sci, Oxford, England
[4] Univ Oxford, Weatherall Inst Mol Med, Oxford, England
[5] Stowers Inst Med Res, Kansas City, MO USA
来源
NATURE CARDIOVASCULAR RESEARCH | 2025年 / 4卷 / 02期
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会; 英国工程与自然科学研究理事会; 英国惠康基金; 欧盟地平线“2020”;
关键词
SUBENDOCARDIAL PURKINJE-FIBERS; DISCONTINUOUS CONDUCTION; VENTRICULAR-ARRHYTHMIAS; IVABRADINE; EXPRESSION; ISCHEMIA; NETWORK; CELLS;
D O I
10.1038/s44161-024-00586-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Arrhythmias are a hallmark of myocardial infarction (MI) and increase patient mortality. How insult to the cardiac conduction system causes arrhythmias following MI is poorly understood. Here, we demonstrate conduction system restoration during neonatal mouse heart regeneration versus pathological remodeling at non-regenerative stages. Tissue-cleared whole-organ imaging identified disorganized bundling of conduction fibers after MI and global His-Purkinje disruption. Single-cell RNA sequencing (scRNA-seq) revealed specific molecular changes to regenerate the conduction network versus aberrant electrical alterations during fibrotic repair. This manifested functionally as a transition from normal rhythm to pathological conduction delay beyond the regenerative window. Modeling in the infarcted human heart implicated the non-regenerative phenotype as causative for heart block, as observed in patients. These findings elucidate the mechanisms underpinning conduction system regeneration and reveal how MI-induced damage elicits clinical arrhythmogenesis.
引用
收藏
页码:163 / 179
页数:33
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