心肌梗塞
有丝分裂
心脏病学
心力衰竭
内科学
医学
心肌细胞
人的心脏
心肌细胞
细胞生物学
细胞
哺乳动物心脏
循环系统
心肌梗死并发症
心肌细胞
细胞生长
作者
Robert D. Hume,Jessica Warwick,Woo Jun Shim,Cassandra Malecki,Mengbo Li,Lakshay Seth,Dylan Harney,Julien Dagher,Trina Lum,Geraldine L. Tierney,Wendy A. Cooper,Eugene Slaughter,Xiaosuo Wang,Lisa Nguyen,Louise Cole,James Edelman,Fairooj N. Rashid,Callum B. Houlahan,Antony Gao,Angela L. Ferguson
出处
期刊:Circulation Research
[Lippincott Williams & Wilkins]
日期:2025-12-04
卷期号:138 (2): e327486-e327486
标识
DOI:10.1161/circresaha.125.327486
摘要
BACKGROUND: Myocardial infarction (MI) is a leading cause of death worldwide and can eliminate up to a third of the cardiomyocytes within the human heart. Although cardiomyocytes undergo mitosis during early development, most cardiomyocytes cease cell cycling soon after birth. In contrast, rodent MI models have shown that cardiomyocytes increase mitosis in response to ischemia; however, this has not been shown in humans. METHODS: Using a unique premortem post-MI human heart, immunostaining, bulk RNA sequencing, proteomics, metabolomics, single-nucleus RNA sequencing and a novel post-MI human biopsy method, we investigated human cardiomyocyte mitosis post-MI. RESULTS: We show that adult human cardiomyocytes exhibit increased mitosis and cytokinesis in response to ischemia. CONCLUSIONS: Future development of therapeutics to enhance this intrinsic mitotic potential could lead to new treatments that reverse heart failure via cardiac regeneration.
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